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Scooped by Dr. Stefan Gruenwald
March 25, 2021 1:34 PM
Scoop.it!

Hi-throughput Simulation of the Immune System to Fight Cancer

Hi-throughput Simulation of the Immune System to Fight Cancer | Amazing Science | Scoop.it

Cancer cells have evolved mechanisms to escape the body's immune defense. Agents that prevent immune escape are attractive targets for the development of new cancer therapies. A group of scientists led by Herbert Waldmann and Slava Ziegler at the Max Planck Institute of Molecular Physiology in Dortmund has now developed a new cell-based test system to identify immunoregulatory modulators. Screening a library of over 150,000 substances revealed several potent substances with unprecedented structure.

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Rescooped by Dr. Stefan Gruenwald from Virus World
March 24, 2021 8:19 PM
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Researchers Race to Develop Antiviral Weapons to Fight the Pandemic Coronavirus

Researchers Race to Develop Antiviral Weapons to Fight the Pandemic Coronavirus | Amazing Science | Scoop.it

An arsenal of potential treatments takes aim at proteins that are key to the virus’ life cycle.  In March 2020, as the full scope of the COVID-19 pandemic was coming into view, Jen Nwankwo and colleagues turned a pair of artificial intelligence (AI) tools against SARS-CoV-2. One newly developed AI program, called SUEDE, digitally screens all known drug-like compounds for likely activity against biomolecules thought to be involved in the disease. The other, BAGEL, predicts how to build inhibitors to known targets. The two programs searched for compounds able to block human enzymes that play essential roles in enabling the virus to infect its host cells. While SUEDE sifted through 14 billion compounds in just a few hours and spat out a hit, BAGEL created equally fast new leads.

 

Nwankwo, CEO of a Massachusetts biotech startup called 1910 Genetics, asked a chemical company partner to synthesize the compounds. A week or so later, her team received the orders, added each compound in turn to human cells, and learned that each blocked its target and prevented viral entry into cells. 1910 Genetics is now looking to partner with antiviral drug developers to pursue animal and human trials.

 

“It shows that AI can massively accelerate drug design,” Nwankwo says. Designing and developing a medicine is almost always painfully slow, regularly taking at least a decade. Many steps—such as animal studies, tweaking molecules to avoid side effects, and clinical trials—can’t be accelerated. But the race toward new treatments against COVID-19 is off to a blistering start as researchers accelerate other parts of the search, deploying supercomputers, robots, synchrotrons, and every other tool they have to find and lab test possible medicines at speed. According to a biotech industry drug tracker, some 239 antiviral molecules against COVID-19 are under development, targeting multiple parts of the viral life cycle.

 

Antivirals have proved critical in fighting other infections such as HIV and hepatitis C. Such drugs will be vital in the struggle against the pandemic coronavirus, too, despite the ongoing rollout of COVID-19 vaccines. “We know not everyone will be able to take the vaccine or respond to it,” says Mark Denison, a virologist at Vanderbilt University. Vaccines may also lose effectiveness as immune protection wanes or viral variants emerge. “So, continuing development of antivirals is critical,” Denison says. To date, most of that search has centered on “repurposed” compounds, antivirals originally developed to combat other diseases. Other repurposed drugs, such as the steroid dexamethasone, target the body’s reaction to infection rather than the virus itself.

 

“Drug repurposing made sense as the first thing to try,” Nwankwo says. Many repurposed antivirals have shown promise against SARS-CoV-2 in cell and animal studies and are now in clinical trials. One, remdesivir, has already proved to speed recovery by a few days in very ill people. But several other repurposed antivirals have failed to prove effective.

 

As a result, says Francis Collins, director of the National Institutes of Health (NIH), “We really, really need a bunch more antivirals.” Buoyed by almost daily advances in understanding SARS-CoV-2, the rapidly growing list of new compounds that might block it, and ongoing clinical trials—some of them late stage—Denison and others hope to deliver effective drugs this year. Says Andrew Mesecar, a structural biologist from Purdue University: “I am confident we will have more treatments for coronavirus.” As viruses go, SARS-CoV-2 is a behemoth, with some 30,000 letters of RNA in its genetic code. Those letters encode 29 viral proteins that enable the virus to infect cells, reproduce, escape, and spread. “We’re fortunate this virus has provided us with so many targets, so many opportunities for intervention,” says Sandra Weller, a molecular biologist at UConn Health. The 29 proteins come in three main categories: structural proteins that make up the outer coat; nonstructural proteins (NSPs), most of which help the virus replicate; and accessory proteins, several of which appear to subdue the host’s immune response. Thus far, drug hunters have taken aim mainly at the structural and replication proteins, concentrating on molecules similar to those that have paid off in fighting other viruses. SARS-CoV-2 has just four structural proteins. The envelope and membrane proteins make up the virus’ spherical shell, and the nucleocapsid protein shields its genome. The fourth protein, spike, protrudes from the shell, creating the crown of thorns that gives the virus its name and enables it to bind to angiotensin-converting enzyme 2 (ACE2) receptors, its main entry point into cells.

 

Spike is the primary target of many vaccines and antivirals. However, small molecules, the typical focus for drug discovery programs, won’t work because they aren’t bulky enough to prevent spike from binding to the ACE2 receptor.vDavid Baker, a computational biologist at the University of Washington, Seattle, and colleagues turned instead to miniproteins, each with about 60 amino acids, customized to block protein-protein interactions. In late 2020, Baker’s team described miniproteins tailormade to bind tightly to the virus’ spike protein and block it from attaching to the ACE2 receptor. The tiny proteins kept the virus from infecting human cells in a test tube, and Baker says miniproteins could make ideal drugs because they are far more stable than conventional protein therapeutics, such as antibodies, which must be refrigerated. Baker is in discussions with drug companies to pursue his leads. Other researchers have a different strategy for interfering with viral binding. They are designing ACE2 look-alikes to serve as decoys, drawing SARS-CoV-2 away from cells. Researchers at Neoleukin Therapeutics and their partners, for example, reported creating a miniprotein, CTC-445.2d, that mimics ACE2, binding tenaciously to spike. The compound protected human cells from infection in vitro. When given to hamsters in a nasal spray, the decoy also prevented them from getting severe disease after they received a normally lethal dose of the virus. Another “receptor trap” molecule, described in November 2020 in the Proceedings of the National Academy of Sciences, also diverted SARS-CoV-2, keeping it from infecting cells in the test tube.....


Via Juan Lama
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March 24, 2021 2:15 PM
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Astronomers image magnetic fields at the edge of M87's black hole

Astronomers image magnetic fields at the edge of M87's black hole | Amazing Science | Scoop.it

The Event Horizon Telescope (EHT) collaboration, who produced the first ever image of a black hole, has revealed today a new view of the massive object at the center of the M87 galaxy: how it looks in polarized light. This is the first time astronomers have been able to measure polarization, a signature of magnetic fields, this close to the edge of a black hole. The observations are key to explaining how the M87 galaxy, located 55 million light-years away, is able to launch energetic jets from its core.

 

University of Illinois at Urbana-Champaign Astronomy and Physics Professor Charles Gammie is part of the EHT theory and simulation working group. Gammie is the Willett Professor of Physics and a founding member of the Illinois Center for Advanced Studies of the Universe (ICASU).  Gammie says, “Our research group at Illinois developed numerical procedures that capture the turbulent flow of gas in the strong gravitational pull of the black hole and then simulate the production and propagation of polarized light, taking into account the black hole's gravitational field. “Illinois graduate students George Wong and Ben Prather played a vital role in creating the simulations used to the analyze the new results. They were also part of the paper writing team for the polarization theory paper published today in The Astrophysical Journal.”

 

The bright jets of energy and matter that emerge from M87’s core and extend at least 5000 light-years from its center are one of the galaxy’s most mysterious and energetic features. Most matter lying close to the edge of a black hole falls in. However, some of the surrounding particles escape moments before capture and are blown far out into space in the form of jets. 

 

Astronomers have relied on different models of how matter behaves near the black hole to better understand this process. But they still don’t know exactly how jets larger than the galaxy are launched from its central region, which is as small in size as the Solar System, nor how exactly matter falls into the black hole. With the new EHT image of the black hole and its shadow in polarized light, astronomers managed for the first time to look into the region just outside the black hole where this interplay between matter flowing in and being ejected out is happening. 

 

These observations provide new information about the structure of the magnetic fields just outside the black hole. The team found that only theoretical models featuring strongly magnetized gas can explain what they are seeing at the event horizon. Researchers at the U of I created such models.

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March 15, 2021 4:59 PM
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There might be many planets with water-rich atmospheres in our galaxy

There might be many planets with water-rich atmospheres in our galaxy | Amazing Science | Scoop.it

An atmosphere is what makes life on Earth's surface possible, regulating our climate and sheltering us from damaging cosmic rays. But although telescopes have counted a growing number of rocky planets, scientists had thought most of their atmospheres long lost.

 

However, a new study by University of Chicago and Stanford University researchers suggests a mechanism whereby these planets could not only develop atmospheres full of water vapor, but keep them for long stretches. Published March 15, 2021 in the Astrophysical Journal Letters, the research expands our picture of planetary formation and could help direct the search for habitable worlds in other star systems.

 

"Our model is saying that these hot, rocky exoplanets should have a water-dominated atmosphere at some stage, and for some planets, it may be quite a long time," said Asst. Prof. Edwin Kite, an expert in how planetary atmospheres evolve over time. As telescopes document more and more exoplanets, scientists are trying to figure out what they might look like. Generally, telescopes can tell you about an exoplanet's physical size, its proximity to its star and if you're lucky, how much mass it has. To go much further, scientists have to extrapolate based on what we know about Earth and the other planets in our own solar system. But the most abundant planets don't seem to be similar to the ones we see around us.

 

"What we already knew from the Kepler mission is that planets a little smaller than Neptune are really abundant, which was a surprise because there are none in our solar system," Kite said. "We don't know for sure what they are made of, but there's strong evidence they are magma balls cloaked in a hydrogen atmosphere."

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Rescooped by Dr. Stefan Gruenwald from Cool Future Technologies
March 12, 2021 12:57 PM
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A New Powerpaste out of Solid Magnesium Hydride for Hydrogen Storage

A New Powerpaste out of Solid Magnesium Hydride for Hydrogen Storage | Amazing Science | Scoop.it

Gasoline and diesel engines, which are powered by fossil fuels, will soon be sidelined by climate change. Instead, new propulsion systems will be required. One fuel with a big potential is hydrogen.

 

Hydrogen vehicles are equipped with a reinforced tank that is fueled at a pressure of 700 bar. This tank feeds a fuel cell, which converts the hydrogen into electricity. This in turn drives an electric motor to propel the vehicle. In the case of passenger cars, this technology is well advanced, with several hundred hydrogen-powered automobiles already in operation on German roads. At the same time, the network of hydrogen stations in Germany is projected to grow from 100 to 400 over the next three years. Yet hydrogen is not currently an option for small vehicles such as electric scooters and motorcycles, since the pressure surge during refilling would be too great.

 

However, researchers from the Fraunhofer Institute for Manufacturing Technology and Advanced Materials IFAM in Dresden have now come up with a hydrogen-based fuel that is ideal for small vehicles: Powerpaste, which is based on solid magnesium hydride. “Powerpaste stores hydrogen in a chemical form at room temperature and atmospheric pressure to be then released on demand,” explains Dr. Marcus Vogt, research associate at Fraunhofer IFAM. And given that Powerpaste only begins to decompose at temperatures of around 250 °C, it remains safe even when an e-scooter stands in the baking sun for hours.

 

Moreover, refueling is extremely simple. Instead of heading to the filling station, riders merely have to replace an empty cartridge with a new one and then refill a tank with mains water. This can be done either at home or underway. The starting material of Powerpaste is magnesium, one of the most abundant elements and, therefore, an easily available raw material. Onboard the vehicle, the Powerpaste is released from a cartridge by means of a plunger. When water is added from an onboard tank, the ensuing reaction generates hydrogen gas in a quantity dynamically adjusted to the actual requirements of the fuel cell. In fact, only half of the hydrogen originates from the Powerpaste ; the rest comes from the added water.

 

“Powerpaste thus has a huge energy storage density,” says Vogt. “It is substantially higher than that of a 700 bar high-pressure tank. And compared to batteries, it has ten times the energy storage density.” This means that Powerpaste offers a range comparable to – or even greater than – gasoline. And it also provides a higher range than compressed hydrogen at a pressure of 700 bar.

 


Via Sepp Hasslberger
Sepp Hasslberger's curator insight, February 19, 2021 7:08 PM

This looks like a much needed advance in our ability to store hydrogen to be released on demand. It might get fuel cells (making electricity from hydrogen) off the ground into more widespread application. 

Wojciech Krawczyk's curator insight, April 3, 2022 4:24 AM
Paliwo na bazie wodoru. Czy będzie to rewolucja na rynku motoryzacji?
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March 10, 2021 4:18 PM
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Wormholes may be lurking throughout the universe—and scientists are proposing new ways to find them

Wormholes may be lurking throughout the universe—and scientists are proposing new ways to find them | Amazing Science | Scoop.it
Albert Einstein's theory of general relativity profoundly changed our thinking about fundamental concepts in physics, such as space and time. But it also left us with some deep mysteries. One was black holes, which were only unequivocally detected over the past few years. Another was "wormholes"—bridges connecting different points in spacetime, in theory providing shortcuts for space travelers.

 

Wormholes are still in the realm of the imagination. But some scientists think we will soon be able to find them, too. Over the past few months, several new studies have suggested intriguing ways forward. Black holes and wormholes are special types of solutions to Einstein's equations, arising when the structure of spacetime is strongly bent by gravity. For example, when matter is extremely dense, the fabric of spacetime can become so curved that not even light can escape. This is a black hole.

 

As the theory allows the fabric of spacetime to be stretched and bent, one can imagine all sorts of possible configurations. In 1935, Einstein and physicist Nathan Rosen described how two sheets of spacetime can be joined together, creating a bridge between two universes. This is one kind of wormhole – and since then many others have been imagined.

 

Some wormholes may be "traversable", meaning humans may be able to travel through them. For that though, they would need to be sufficiently large and kept open against the force of gravity, which tries to close them. To push spacetime outward in this way would require huge amounts of "negative energy".

 

Sounds like sci-fi? We know that negative energy exists, small amounts have already been produced in the lab. We also know that negative energy is behind the universe's accelerated expansion. So nature may have found a way to make wormholes.

 

Spotting wormholes in the sky

How can we ever prove that wormholes exist? In a new paper, published in the Monthly Notices of the Royal Society, Russian astronomers suggest they may exist at the center of some very bright galaxies, and propose some observations to find them. This is based on what would happen if matter coming out of one side of the wormhole collided with matter that was falling in. The calculations show that the crash would result in a spectacular display of gamma rays that we could try to observe with telescopes.

 

This radiation could be the key to differentiating between a wormhole and a black hole, previously assumed to be indistinguishable from the outside. But black holes should produce fewer gamma rays and eject them in a jet, while radiation produced via a wormhole would be confined to a giant sphere. Although the kind of wormhole considered in this study is traversable, it would not make for a pleasant trip. Because it would be so close to the center of an active galaxy, the high temperatures would burn everything to a crisp. But this wouldn't be the case for all wormholes, such as those further from the galactic center.

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Rescooped by Dr. Stefan Gruenwald from Virus World
March 6, 2021 3:45 PM
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Biologists Find Almost 143,000 Bacteriophage Species in Human Gut 

Biologists Find Almost 143,000 Bacteriophage Species in Human Gut  | Amazing Science | Scoop.it

A team of biologists from the Wellcome Sanger Institute, the European Bioinformatics Institute and the Universidad de los Andes has identified 142,809 species of bacteriophages -- viruses that infect and replicate in bacteria -- living in the human gut. 

 

Using a DNA-sequencing method called metagenomics, Wellcome Sanger Institute’s Dr. Luis Camarillo-Guerrero and colleagues explored and catalogued the biodiversity of the viral species found in 28,060 public human gut metagenomes and 2,898 bacterial isolate genomes cultured from the human gut. “It’s important to remember that not all viruses are harmful, but represent an integral component of the gut ecosystem,” said co-author Dr. Alexandre Almeida, a postdoctoral researcher at the European Bioinformatics Institute and the Wellcome Sanger Institute. “For one thing, most of the viruses we found have DNA as their genetic material, which is different from the pathogens most people know, such as SARS-CoV-2 or Zika, which are RNA viruses.”

 

“Secondly, these samples came mainly from healthy individuals who didn’t share any specific diseases.” “It’s fascinating to see how many unknown species live in our gut, and to try and unravel the link between them and human health.” The researchers also identified a previously unknown clade of bacteriophages, named Gubaphage. This was found to be the second most prevalent virus clade in the human gut, after crAssphage, which was discovered in 2014.

 

“An important aspect of our work was to ensure that the reconstructed viral genomes were of the highest quality,” Dr. Camarillo-Guerrero said. “A stringent quality control pipeline coupled with a machine learning approach enabled us to mitigate contamination and obtain highly complete viral genomes.” “High-quality viral genomes pave the way to better understand what role viruses play in our gut microbiome, including the discovery of new treatments such as antimicrobials from bacteriophage origin.”

 

The team’s results form the basis of the Gut Phage Database, a highly curated database of phage genomes that will be an invaluable resource for those studying bacteriophages and the role they play on regulating the health of both our gut bacteria and ourselves. “Bacteriophage research is currently experiencing a renaissance,” said Dr. Trevor Lawley, a researcher at the Wellcome Sanger Institute. “This high-quality, large-scale catalogue of human gut viruses comes at the right time to serve as a blueprint to guide ecological and evolutionary analysis in future virome studies.”

 

Findings published in Cell (Feb. 18, 2021):

https://doi.org/10.1016/j.cell.2021.01.029


Via Juan Lama
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Scooped by Dr. Stefan Gruenwald
March 6, 2021 3:25 PM
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An Atom Pushed to Its Speed Limit

An Atom Pushed to Its Speed Limit | Amazing Science | Scoop.it
Researchers have transported an atom between two locations in the shortest possible time, an achievement that has implications for quantum technologies.

 

Moving information from one place to another takes time, even in the quantum world. A team of researchers has now moved an atom in the shortest time possible, in a way that preserves the information that it contains [1]. Achieving the top overall speed turned out to require a series of accelerations and decelerations, not a constant cruise. Disturbances from the environment degrade the performance of quantum computers, and carrying out the calculations as quickly as possible is one way to reduce such effects. But running calculations too quickly can also lead to information loss, so there is a “speed limit” on such systems.

 

For simple, two-level quantum systems, such as an electron (which can be spin-up or spin-down), researchers have performed quantum operations at the theoretically predicted speed limits. However, some quantum technologies, such as atom interferometers, require a system to move among many quantum states. These systems should also have speed limits, but they have not been predicted or measured. Andrea Alberti of the University of Bonn in Germany and his colleagues have now studied an example of such a speed limit. They measured the fastest speed at which an atom could be moved from one place to another, ending at the new location in the same state in which it began, despite transitioning to other states during the trip. Moving too rapidly can cause the atom to end up in a different state, which means that it loses information. Keeping the information safe while moving as fast as possible is a bit like transferring a bowl containing water from one location to another at the highest possible speed that avoids a spill.

 

For their experiments, the team used a so-called optical lattice trap, in which atoms sit in a row of potential energy valleys produced by a pair of overlapping, oppositely directed laser beams. They used a microwave field to cool the atoms to their lowest (ground) vibrational state. In this state, each atom is like a fluid sloshing back and forth in a bowl with the smallest possible amplitude; excited states correspond to larger-amplitude oscillations. The goal was to end in the ground state, even though the atoms transitioned to excited states along the way.

 

To transport the atoms, the team caused the valleys to move like a conveyor belt, with each valley moving as far as its nearest neighbor. They could vary the speed of the conveyor belt, and they used measurement techniques that allowed sub-nanometer tracking of the motion. Alberti and his colleagues transported their atoms a distance of 0.5 micrometers using both constant-speed and variable-speed schemes. In each case, the researchers measured the fidelity, a parameter characterizing the similarity of the initial and final states. The protocol with the best fidelity involved a series of speedups and slowdowns. These speed “wiggles” canceled out the effects of transitions to excited states that occurred during the transport process, ensuring that the atoms ended in the ground state. This wiggling is analogous to physically wiggling a bowl containing water to counteract excessive sloshes as it is moved at high speed—tipping it forward a bit at the beginning of its journey and backward a bit at the end.

 

The researchers found that when the average speed over the trip was below about 17 millimeters per second, the fidelity was very good, but it dropped to much lower values for higher average speeds. The team developed a theory to explain this measured speed limit. “The finding is a compelling demonstration of how fundamental properties of quantum dynamics change when one goes beyond the well-studied case of a two-level system,” says Nora Tischler, a quantum physicist at Griffith University in Australia. “I am excited by this work,” she adds. Daniel Burgarth of Macquarie University, also in Australia, is equally impressed. He hopes that the new method will be adapted by other groups to operate complex quantum systems at or near their speed limits.

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March 6, 2021 3:13 PM
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New study suggests supermassive black holes could form from dark matter

New study suggests supermassive black holes could form from dark matter | Amazing Science | Scoop.it

A new theoretical study has proposed a novel mechanism for the creation of supermassive black holes from dark matter. The international team find that rather than the conventional formation scenarios involving ‘normal’ matter, supermassive black holes could instead form directly from dark matter in high density regions in the centers of galaxies. The result has key implications for cosmology in the early Universe, and is published in Monthly Notices of the Royal Astronomical Society.

 

Exactly how supermassive black holes initially formed is one of the biggest problems in the study of galaxy evolution today. Supermassive black holes have been observed as early as 800 million years after the Big Bang, and how they could grow so quickly remains unexplained.

 

Standard formation models involve normal baryonic matter – the atoms and elements that that make up stars, planets, and all visible objects – collapsing under gravity to form black holes, which then grow over time. However the new work investigates the potential existence of stable galactic cores made of dark matter, and surrounded by a diluted dark matter halo, finding that the centers of these structures could become so concentrated that they could also collapse into supermassive black holes once a critical threshold is reached. According to the model this could have happened much more quickly than other proposed formation mechanisms, and would have allowed supermassive black holes in the early Universe to form before the galaxies they inhabit, contrary to current understanding.

 

Carlos R. Argüelles, the researcher at Universidad Nacional de La Plata and ICRANet who led the investigation comments: “This new formation scenario may offer a natural explanation for how supermassive black holes formed in the early Universe, without requiring prior star formation or needing to invoke seed black holes with unrealistic accretion rates.” Another intriguing consequence of the new model is that the critical mass for collapse into a black hole might not be reached for smaller dark matter halos, for example those surrounding some dwarf galaxies. The authors suggest that this then might leave smaller dwarf galaxies with a central dark matter nucleus rather than the expected black hole. Such a dark matter core could still mimic the gravitational signatures of a conventional central black hole, whilst the dark matter outer halo could also explain the observed galaxy rotation curves.

 

“This model shows how dark matter haloes could harbor dense concentrations at their centers, which may play a crucial role in helping to understand the formation of supermassive black holes,” added Carlos.

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Scooped by Dr. Stefan Gruenwald
March 6, 2021 3:07 PM
Scoop.it!

Beauty is in the brain of the beholder: An AI generates personally attractive images by reading brain data

Beauty is in the brain of the beholder: An AI generates personally attractive images by reading brain data | Amazing Science | Scoop.it

Researchers have succeeded in making an AI understand our subjective notions of what makes faces attractive. The device demonstrated this knowledge by its ability to create new portraits on its own that were tailored to be found personally attractive to individuals. The results can be utilized, for example, in modelling preferences and decision-making as well as potentially identifying unconscious attitudes.

 

"In our previous studies, we designed models that could identify and control simple portrait features, such as hair colour and emotion. However, people largely agree on who is blond and who smiles. Attractiveness is a more challenging subject of study, as it is associated with cultural and psychological factors that likely play unconscious roles in our individual preferences. Indeed, we often find it very hard to explain what it is exactly that makes something, or someone, beautiful: Beauty is in the eye of the beholder," says Senior Researcher and Docent Michiel Spapé from the Department of Psychology and Logopedics, University of Helsinki.

 

The study, which combines computer science and psychology, was published in February in the IEEE Transactions in Affective Computing journal.

 

Preferences exposed by the brain

Initially, the researchers gave a generative adversarial neural network (GAN) the task of creating hundreds of artificial portraits. The images were shown, one at a time, to 30 volunteers who were asked to pay attention to faces they found attractive while their brain responses were recorded via electroencephalography (EEG).

"It worked a bit like the dating app Tinder: the participants 'swiped right' when coming across an attractive face. Here, however, they did not have to do anything but look at the images. We measured their immediate brain response to the images," Spapé explains.

The researchers analysed the EEG data with machine learning techniques, connecting individual EEG data through a brain-computer interface to a generative neural network.

 

"A brain-computer interface such as this is able to interpret users' opinions on the attractiveness of a range of images. By interpreting their views, the AI model interpreting brain responses and the generative neural network modelling the face images can together produce an entirely new face image by combining what a particular person finds attractive," says Academy Research Fellow and Associate Professor Tuukka Ruotsalo, who heads the project.

 

Reference: Michiel Spape, Keith Davis, Lauri Kangassalo, Niklas Ravaja, Zania Sovijarvi-Spape, Tuukka Ruotsalo. Brain-computer interface for generating personally attractive images. IEEE Transactions on Affective Computing, 2021; 1 DOI: 10.1109/TAFFC.2021.3059043

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Scooped by Dr. Stefan Gruenwald
March 6, 2021 2:58 PM
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Fungi in the Gut Prime Immunity Against Infections

Fungi in the Gut Prime Immunity Against Infections | Amazing Science | Scoop.it
Common fungi, often present in the gut, teach the immune system how to respond to their more dangerous relatives, according to new research from scientists at Weill Cornell Medicine.

 

The a recent study, published Feb. 5, 2021 in Cell, reveals a new twist in the complex relationship between humans and their associated microbes, and points the way toward novel therapies that could help combat a rising tide of drug-resistant pathogens.

The new discovery stemmed from work on inflammatory bowel disease, which often causes patients to carry larger than normal populations of fungi in their guts. These patients often develop strong antibody responses against mannan, a molecule common to a wide range of fungal species. However, Dr. Iliyan Iliev, associate professor of immunology in medicine in the Division of Gastroenterology and Hepatology at Weill Cornell Medicine, noticed that healthy controls in these studies also had some level of anti-fungal antibodies. "There was no actual evidence for fungal infections in the healthy individuals that we examined, so we started thinking about the possible function of those antibodies," said Dr. Iliev, who is senior author on the study and a member of the Jill Roberts Institute for Research in Inflammatory Bowel Disease.

 

The team developed a platform that allowed them to determine which gut fungi are targeted by antibodies in the blood of individual patients. They detected a strong response against the yeast Candida albicans. Turning to experiments in mice, Dr. Iliev and Itai Doron, a Weill Cornell Medicine Graduate School of Medical Sciences doctoral candidate in the lab and lead author on the study, found that colonizing the animals' guts with Candida albicans caused them to develop antibodies against the fungus in their bloodstreams, even though they didn't develop blood-borne fungal infections. Instead, the animals' immune cells appeared to transport fungal antigens to the spleen, stimulating the production of circulating antibodies in the bloodstream. "Those fungi just educate that immune response," Dr. Iliev said.

 

In patients with suppressed immune systems, such as organ transplant recipients and some cancer patients, fungi in the gut can invade the bloodstream and cause life-threatening infections. Dr. Iliev and his colleagues mimicked this process by treating mice with immunosuppressive drugs. When a Candida species colonizes the gut of these mice, the fungus moves into the bloodstream, causing a fatal infection. Treating the mice with purified anti-fungal antibodies from donor animals protected the immunosuppressed mice from these infections. The same strategy worked against infection with either Candida albicans or the emerging pathogenic yeast Candida auris, which has become a major cause of fungal disease in immunosuppressed patients and the elderly in recent years.

george sperco's curator insight, February 7, 2023 1:55 PM
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Crediamo che i farmaci a volte possano essere molto urgenti da assumere. Se hai urgente bisogno di farmaci, possiamo anche fornirti una consegna espressa,


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Life from deep down: A new translucent snail discovered from the deepest cave in Croatia

Life from deep down: A new translucent snail discovered from the deepest cave in Croatia | Amazing Science | Scoop.it

Scientists discovered a new species of a peculiar cave-dwelling snail in one of the 20 deepest cave systems in the world, Lukina Jama–Trojama in Croatia. The newly discovered species belongs to a genus of minute air-breathing land snails that have lost visual orientation and are considered to be true eutroglobionts, or exclusive cave-dwellers.

 

The study describing the new species was published in the open access journal Subterranean Biology. The new species Zospeum tholussum is a miniature and fragile snail, with a beautifully shaped dome-like translucent shell. Only one living specimen was found during the expedition around the galleries of the Lukina Jama–Trojama cave system. The animal was found at the remarkable depth of 980 m, in an unnamed chamber full of rocks and sand and a small stream running through it.

 

All known species from the cave-dwelling genus Zospeum possess a limited ability to move. Their preference of a muddy habitat and the fact that they are usually located near the drainage system of the cave, in a close proximity to running water, however suggest that these animals are not exactly immobile. Scientists hypothesize that dispersal is achieved through passive transportation via water or larger mammals.

 

The Lukina Jama–Trojama is the deepest cave system in Croatia, extraordinary for its vertical shape, long pits and great depth of -1392 m. From an ecological point of view this cave system is extremely interesting for having three microclimatic layers: firstly entrance icy part with the temperature of about 1 °C, secondly, middle part with the temperature up to 2 °C and bottom part with temperature till 4 °C. These unusual living conditions make the cave extremely interesting for scientist from a biodiversity point of view.

 

Citation: Weigand AM (2013) New Zospeum species (Gastropoda, Ellobioidea, Carychiidae) from 980 m depth in the Lukina Jama–Trojama cave system (Velebit Mts., Croatia). Subterranean Biology 11: 45–53. doi: 10.3897/ subtbiol.11.5966

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March 5, 2021 1:03 PM
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Hybrid chips can run AI on battery-powered devices

Hybrid chips can run AI on battery-powered devices | Amazing Science | Scoop.it
In traditional electronics, separate chips process and store data, wasting energy as they toss data back and forth over what engineers call a “memory wall.” New algorithms combine several energy-efficient hybrid chips to create the illusion of one mega–AI chip.

 

Smartwatches and other battery-powered electronics would be even smarter if they could run AI algorithms. But efforts to build AI-capable chips for mobile devices have so far hit a wall – the so-called “memory wall” that separates data processing and memory chips that must work together to meet the massive and continually growing computational demands imposed by AI.

 

Hardware and software innovations give eight chips the illusion that they’re one mega-chip working together to run AI. “Transactions between processors and memory can consume 95 percent of the energy needed to do machine learning and AI, and that severely limits battery life,” said computer scientist Subhasish Mitra, senior author of a new study published in Nature Electronics.

 

Now, a team that includes Stanford computer scientist Mary Wootters and electrical engineer H.-S. Philip Wong has designed a system that can run AI tasks faster, and with less energy, by harnessing eight hybrid chips, each with its own data processor built right next to its own memory storage. This recent paper builds on the team’s prior development of a new memory technology, called RRAM, that stores data even when power is switched off – like flash memory – only faster and more energy efficiently. Their RRAM advance enabled the Stanford researchers to develop an earlier generation of hybrid chips that worked alone.

 

Their latest design incorporates a critical new element: algorithms that meld the eight, separate hybrid chips into one energy-efficient AI-processing engine.

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March 25, 2021 1:31 PM
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On-chip torsion balance with femtonewton (fN) force resolution at room temperature

On-chip torsion balance with femtonewton (fN) force resolution at room temperature | Amazing Science | Scoop.it

The torsion balance contains a rigid balance beam suspended by a fine thread as an ancient scientific instrument that continues to form a very sensitive force sensor to date. The force sensitivity is proportional to the lengths of the beam and thread and inversely proportional to the fourth power of the diameter of the thread. Therefore, nanomaterials that support the torsion balances should be ideal building blocks.

 

In a new report now published on Science Advances, Lin Cong and a research team in quantum physics, microelectronics and nanomaterials in China have detailed a torsional balance array on a chip with the highest sensitivity level. The team facilitated this by using a carbon nanotube as the thread and a monolayer graphene coated with aluminum films as the beam and mirror. Using the experimental setup, Cong et al. measured the femtonewton force exerted by a weak laser. The balances on the chip served as an ideal platform to investigate fundamental interactions up to zeptonewton in accuracy.

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March 24, 2021 2:25 PM
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Microscope that detects individual viruses could power rapid diagnostics

Microscope that detects individual viruses could power rapid diagnostics | Amazing Science | Scoop.it

A fast, low-cost technique to see and count viruses or proteins from a sample in real time, without any chemicals or dyes, could underpin a new class of devices for rapid diagnostics and viral load monitoring, including HIV and the virus that causes COVID-19.

 

Researchers at the University of Illinois Urbana-Champaign described the technique, called Photonic Resonator Interferometric Scattering Microscopy, or PRISM, in the journal Nature Communications.

 

“We have developed a new form of microscopy that amplifies the interaction between light and biological materials. We can use it for very rapid and sensitive forms of diagnostic testing, and also as a very powerful tool for understanding biological processes at the scale of individual items, like counting individual proteins or recording individual protein interactions,” said study leader Brian Cunningham, the Intel Alumni Endowed Chair of electrical and computer engineering at Illinois.

 

In optical microscopes, light bounces off any molecules or viruses it encounters on a slide, creating a signal. Instead of a regular glass slide, the PRISM technique uses a photonic crystal — a nanostructured glass surface that brilliantly reflects only one specific wavelength of light. Cunningham’s group designed and fabricated a photonic crystal that reflects red light, so that the light from a red laser would be amplified.

 

“The molecules we are looking at – in this study, viruses and small proteins – are extremely small. They cannot scatter enough light to create a signal that can be detected by a conventional optical microscope,” said graduate student Nantao Li, the first author of the paper. “The benefit of using the photonic crystal is that it amplifies the light’s intensity so it’s easier to detect those signals and enables us to study these proteins and viruses without any chemical labels or dyes that might modify their natural state or hinder their activity – we can just use the intrinsic scattering signal as the gauge for determining if those molecules are present.”

 

The researchers verified their technique by detecting the virus that causes COVID-19. PRISM detected individual coronaviruses as they traveled across the slide’s surface. The researchers also used PRISM to detect individual proteins such as ferritin and fibrinogen. The technique could allow researchers to study such biological targets in their natural states – watching as proteins interact, for example – or researchers could seed the surface of the photonic crystal slide with antibodies or other molecules to capture the targeted items and hold them in place.

 

“It takes 10 seconds to get a measurement, and in that time we can count the number of viruses captured on the sensor,” Cunningham said. “It’s a single-step detection method that works at room temperature. It is also fast, very sensitive and low cost. It’s very different from the standard way we do viral testing now, which involves breaking open the viruses, extracting their genetic material and putting it through a chemical amplification process so we can detect it. That method, called PCR, is accurate and sensitive, but it requires time, specialized equipment and trained technicians.”

 
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Many People Who Die of COVID-19 Have the Virus in Their Hearts

Many People Who Die of COVID-19 Have the Virus in Their Hearts | Amazing Science | Scoop.it

Three-quarters of people who died of COVID-19 harbored the SARS-CoV-2 virus in their hearts, according to the most detailed study of cardiac tissue to date. Those people were also more likely than patients without cardiac invasion to experience abnormal heart rhythms before they ultimately died.

 

The study offers insight into how the disease may damage the heart—and how certain treatments may help to fight this. The findings “paint a clear picture” about the connection between the virus and heart problems, says Joseph Maleszewski, a cardiovascular pathologist at the Mayo Clinic who was not involved with the study.

 

Scientists have ample evidence of heart damage in COVID-19 patients. Some people, for example, show elevated levels of troponins, molecules released in the blood when the heart muscle is injured. Others have experienced inflammation of the pericardium surrounding the heart—and inflammation of the heart itself. But it’s been unclear whether these problems were caused by the SARS-CoV-2 virus attacking the heart directly, or the damage is due to an overactive immune system response. Previous studies were mixed about whether SARS-CoV-2 can invade heart tissue. Many that haven’t detected the virus use RT-PCR, says James Stone, a cardiovascular pathologist at Massachusetts General Hospital.

 

RT-PCR works by detecting viral RNA in tissue, then making many DNA copies of it. Once there’s enough DNA, a fluorescent tag can stick to it and shine to reveal its presence. But Stone says that heart tissue is often processed and preserved using chemicals like paraffin, which can break down the RNA and prevent detection to begin with. Thus, he and his team used another approach: in situ hybridization and NanoString transcriptomic profiling. Like RT-PCR, these techniques use special molecules to attach to and detect pieces of viral RNA, but they do so without having to make DNA copies first. The approach can identify viral RNA even after it’s broken into smaller pieces. The scientists also analyzed about 1,000 pieces of heart tissue—more than 20 samples from each of the 41 patients they looked at. That’s double the number of samples per patient in most studies, Stone says. 

 

SARS-CoV-2 was present in 30 of the hearts, the team reports today in Modern Pathology. And only those patients experienced new atrial fibrillations, fast and irregular heart rhythms, or early or extra heartbeats, compared with the other patients in the study—a correlation Stone calls “pretty phenomenal.” Still, it’s unclear whether the virus attacked the heart directly in these cases. Most of the infected cardiac cells were immune cells, which SARS-CoV-2 could have invaded elsewhere in the body before they traveled to the heart. It’s also unclear whether the virus—rather than the immune cells themselves—is causing the problems.

 

Regardless, the study may help explain why the steroid dexamethasone is so helpful to some patients. The drug was one of the first found to prevent deaths from severe COVID-19. It reduces inflammation, so it may have curbed the presence of SARS-CoV-2–harboring immune cells in the heart, Stone says. Only 50% of the patients treated with dexamethasone had the virus in their hearts, compared with 90% of patients who were not on the drug. But compared with large clinical trials, the number of patients in this new study is small, making it impossible to say that one drug protects the heart better than another, says Nicholas Hendren, a cardiology fellow at the University of Texas Southwestern Medical Center. Still, Maleszewski says the new findings are a call to action. Scientists need to probe more cardiac tissue, he argues, not just to see how COVID-19 kills patients, but to figure out how it hurts the hearts of those that survive. The disease may, for example, create scar tissue that can cause cardiac problems down the line. We’re starting to understand what COVID-19 does to patients when they have it, he says. “What’s not clear is what happens later on.”

 

This Research is Published in Modern Pathology (March 17, 2021):

https://doi.org/10.1038/s41379-021-00790-1 


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Rescooped by Dr. Stefan Gruenwald from Cool Future Technologies
March 12, 2021 12:59 PM
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Spacetime wave packets: New class of laser defies laws of light physics

Spacetime wave packets: New class of laser defies laws of light physics | Amazing Science | Scoop.it
Scientists have created a new class of laser beam that appears to violate long-held laws of light physics. These new beams, which the team calls “spacetime wave packets,” follow different rules of refraction, which could lead to new communication technologies

 

Light travels at different speeds through different media, slowing down in denser materials. It’s a phenomenon that’s best summed up in a basic, middle-school science experiment: if you place a spoon in a glass of water, the spoon will appear to be broken at the water’s surface. That’s because the light is traveling slower through the water than the air, and the light rays bend as they enter the water – a phenomenon known as Snell’s Law.

 

But the new laser beams don’t follow this basic law of light. And it’s not just Snell’s Law either – the team says they also ignore Fermat’s Principle, which says that light always takes the shortest possible path. “This new class of laser beams has unique properties that are not shared by common laser beams,” says Ayman Abouraddy, principal investigator of the study. “Spacetime wave packets can be arranged to behave in the usual manner, to not change speed at all, or even to anomalously speed up in denser materials. As such, these pulses of light can arrive at different points in space at the same time.”

 

This has some major implications for optical communications technologies. The team uses the example of a plane sending messages encoded in light to two submarines, at the same depth but different distances away. Normally, the message would arrive at the closer sub first, but with spacetime wave packets the pulses could be propagated to reach both at the exact same time.


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Sepp Hasslberger's curator insight, August 8, 2020 6:39 AM

We are learning about light...

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Birds learn to avoid flashy, hard-to-catch butterflies and their lookalikes

Birds learn to avoid flashy, hard-to-catch butterflies and their lookalikes | Amazing Science | Scoop.it
The showy colors of some butterflies could advertise their speed and nimbleness, much like a coat of bright yellow paint on a sports car. A new study shows birds can learn to recognize these visual cues, avoiding not only butterflies they've failed to nab in the past but similar-looking species as well.

 

The research provides some of the strongest evidence to date for the idea of evasive mimicry, a strategy in which animals protect themselves from predators by matching the colors or patterns of agile relatives. First proposed more than 60 years ago, the hypothesis has been a challenge to test. But in an experimental setting, researchers found that wild birds learned and remembered the wing patterns of artificial butterflies that evaded their attacks, as well as those that had a foul flavor, equally spurning both in follow-up tests and often ignoring lookalikes with similar color patterns. Unexpectedly, the birds learned to avoid evasive butterflies faster than distasteful ones.

 

The results suggest that being hard to catch may deter predators at least as effectively as chemical defenses. "There's a common idea that being distasteful is one of the best kinds of defense to have, but at least in this experiment, that didn't prove to be the case," said study co-author Keith Willmott, curator and director of the Florida Museum of Natural History's McGuire Center for Lepidoptera and Biodiversity.

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March 10, 2021 4:12 PM
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Neanderthals disappeared from Europe earlier than thought, study suggests

Neanderthals disappeared from Europe earlier than thought, study suggests | Amazing Science | Scoop.it

Neanderthal fossils from a cave in Belgium believed to belong to the last survivors of their species ever discovered in Europe are thousands of years older than once thought, a new study said.

 

Previous radiocarbon dating of the remains from the Spy Cave yielded ages as recent as approximately 24,000 years ago, but the new testing pushes the clock back to between 44,200 to 40,600 years ago. The research appeared in the Proceedings of the National Academy of Sciences and was carried out by a team from Belgium, Britain and Germany.

 

Co-lead author Thibaut Deviese from the University of Oxford and Aix-Marseille University told AFP he and colleagues had developed a more robust method to prepare samples, which was better able to exclude contaminants. Having a firm idea of when our closest human relatives disappeared is considered a key first step toward understanding more about their nature and capabilities, as well as why they eventually went extinct while our own ancestors prospered.

 

The new method still relies on radiocarbon dating, long considered the gold standard of archeological dating, but refines the way specimens are collected. All living things absorb carbon from the atmosphere and their food, including the radioactive form carbon-14, which decays over time. Since plants and animals stop absorbing carbon-14 when they die, the amount that remains when they are dated tells us how long ago they lived.

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Researchers create quantum light source that is 1,000-fold brighter than others

Researchers create quantum light source that is 1,000-fold brighter than others | Amazing Science | Scoop.it

Quantum technologies such as quantum computers require sources of entangled pairs of photons. To make these photon pairs, researchers commonly use silicon-based devices, where the silicon sits on an insulator.

 

Galan Moody and his colleagues at the University of California, Santa Barbara, wondered if they could switch the silicon with aluminum gallium arsenide (AlGaAs), a material that has recently been demonstrated to be useful for classical photonics applications. The team showed that AlGaAs-made devices can produce entangled photons at a rate 1000 times greater than devices made from other materials [1].

 

Chip-sized devices for producing entangled pairs of photons typically couple laser light into a photonic waveguide or an optical cavity. Individual photons in the laser are then annihilated by interacting with the cavity’s material, a process that creates two new—entangled—photons. The efficiency of this process depends on the size of the cavity and the properties of the material used to make it.

 

Using this same design, Moody and his colleagues tinkered with the cavity’s size and switched its material from silicon to AlGaAs. They found that they could increase the efficiency of the process significantly without compromising other important properties of the generated entangled photon pairs, such as entanglement fidelity.

 

The 1000-fold increase in brightness that the team achieved should, they say, let them produce the same number of entangled photon pairs as other devices but by using lower-power lasers. That could allow the modified devices to consume less power overall. AlGaAs could also be used to make the other components for quantum computers, potentially allowing them to be contained on a single chip. The team says that such integration would simplify device fabrication and facilitate all-on-chip quantum-photonics systems.

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Ultralight materials: High strength through hierarchy

Ultralight materials: High strength through hierarchy | Amazing Science | Scoop.it

As light as possible and as strong as possible at the same time. These are the requirements for modern lightweight materials, such as those used in aircraft construction and the automotive industry. A research team has now developed a new materials' design approach for future ultralight materials: Nanometer-sized metal struts that form nested networks on separate hierarchical levels provide amazing strength.

 

When the Eiffel Tower was inaugurated in 1889, it was considered a technical marvel. Its artful and delicate arrangement of large and small iron girders provided extraordinary stability and made sure it became the world's tallest building at the time by a long shot. "Hierarchical" is what experts call the engineering approach of an open array of larger beams braced by smaller ones. For several years now, material science researchers have tried to transfer this efficient approach to the internal microstructure of materials, for example by using 3D printers that can replicate engineering truss structures on a micrometer scale.

 

So far, hopes of creating a new generation of extremely strong lightweight construction materials have not been fulfilled. One of the reasons: "A 3D printer can only print a maximum of roughly ten thousand beams and that will take hours," according to Professor Jörg Weißmüller of the Institute of Materials Mechanics at HZG, co-author of the current publication. "For practical applications, this is not really a viable option."

 

Corroding away silver

Nevertheless, his team is pursuing an even more ambitious goal. The vision: If beams could be strengthened by downsizing to few nanometers in diameter, they could provide the basis for a new type of material -- exceptionally light and at the same time strong. However, this kind of material would have to contain trillions of beams, far exceeding the capability of even the most sophisticated printer. "That is why we have to trick nature into making these kinds of materials for us, simply by self-organization," Weißmüller's colleague Dr. Shan Shi, lead author of the study, explains.

 

As a start, the team used an alloy of 93% silver and 7% gold. This alloy is dipped into diluted sulfuric acid, dissolving out approximately half of the silver. As a result, the remaining material rearranges itself, forming a delicate network of nanoscale beams. Afterwards, the material undergoes a heat treatment at several hundred degrees. "This coarsens the network to a beam size of 150 nanometers while maintaining the original architecture," Shi explains. During the last step, acid comes into play once again. It is used to wash out the rest of the silver, leaving only gold beams with a pore size of 15 nanometers on average. The result is a hierarchically structured material with two distinctly different beam sizes, not unlike the Eiffel Tower. As a result of its open network structure, this new material consists of 80 to 90% air, giving it a density of only 10 to 20% of the solid metal.

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Can’t solve a riddle? The answer might lie in knowing what doesn’t work

Can’t solve a riddle? The answer might lie in knowing what doesn’t work | Amazing Science | Scoop.it

Ever get stuck trying to solve a puzzle? You look for a pattern, or a rule, and you just can't spot it. So you back up and start over. That's your brain recognizing that your current strategy isn't working, and that you need a new way to solve the problem, according to new research from the University of Washington. With the help of about 200 puzzle-takers, a computer model and functional MRI (fMRI) images, researchers have learned more about the processes of reasoning and decision-making, pinpointing the brain pathway that springs into action when problem-solving goes south.

 

"There are two fundamental ways your brain can steer you through life -- toward things that are good, or away from things that aren't working out," said Chantel Prat, associate professor of psychology and co-author of the new study, published Feb. 23 2021, in the journal Cognitive Science. "Because these processes are happening beneath the hood, you're not necessarily aware of how much driving one or the other is doing." Using a decision-making task developed by Michael Frank at Brown University, the researchers measured exactly how much "steering" in each person's brain involved learning to move toward rewarding things as opposed to away from less-rewarding things. Prat and her co-authors were focused on understanding what makes someone good at problem-solving.

 

The research team first developed a computer model that specified the series of steps they believed were required for solving the Raven's Advanced Performance Matrices (Raven's) -- a standard lab test made of puzzles like the one above. To succeed, the puzzle-taker must identify patterns and predict the next image in the sequence. The model essentially describes the four steps people take to solve a puzzle:

  • Identify a key feature in a pattern;
  • Figure out where that feature appears in the sequence;
  • Come up with a rule for manipulating the feature;
  • Check whether the rule holds true for the entire pattern.

 

At each step, the model evaluated whether it was making progress. When the model was given real problems to solve, it performed best when it was able to steer away from the features and strategies that weren't helping it make progress. According to the authors, this ability to know when your "train of thought is on the wrong track" was central to finding the correct answer.

 

The next step was to see whether this was true in people. To do so, the team had three groups of participants solve puzzles in three different experiments. In the first, they solved the original set of Raven's problems using a paper-and-pencil test, along with Frank's test which separately measured their ability to "choose" the best options and to "avoid" the worse options. Their results suggested that only the ability to "avoid" the worst options related to problem-solving success. There was no relation between one's ability to recognize the best choice in the decision-making test, and to solve the puzzles effectively.

 

The second experiment replaced the paper-and-pencil version of the puzzles with a shorter, computerized version of the task that could also be implemented in an MRI brain-scanning environment. These results confirmed that those who were best at avoiding the worse options in the decision-making task were also the best problem solvers.

 

The final group of participants completed the computerized puzzles while having their brain activity recorded using fMRI. Based on the model, the researchers gauged which parts of the brain would drive problem-solving success. They zeroed in on the basal ganglia -- what Prat calls the "executive assistant" to the prefrontal cortex, or "CEO" of the brain. The basal ganglia assist the prefrontal cortex in deciding which action to take using parallel paths: one that turns the volume "up" on information it believes is relevant, and another that turns the volume "down" on signals it believes to be irrelevant. The "choose" and "avoid" behaviors associated with Frank's decision-making test relate to the functioning of these two pathways. Results from this experiment suggest that the process of "turning down the volume" in the basal ganglia predicted how successful participants were at solving the puzzles.

 

"Our brains have parallel learning systems for avoiding the least good thing and getting the best thing. A lot of research has focused on how we learn to find good things, but this pandemic is an excellent example of why we have both systems. Sometimes, when there are no good options, you have to pick the least bad one! What we found here was that this is even more critical to complex problem-solving than recognizing what's working."

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March 6, 2021 3:03 PM
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A Single Gene Alteration May Explain Cognitive Differences Between Modern Humans and Their Predecessor

A Single Gene Alteration May Explain Cognitive Differences Between Modern Humans and Their Predecessor | Amazing Science | Scoop.it

UCSD researchers have discovered a single gene alteration that may help explain cognitive differences between modern humans and our predecessor, and used that information to develop Neanderthal-like brain organoids in the lab.

 

As a professor of pediatrics and cellular and molecular medicine at University of California San Diego School of Medicine, Alysson R. Muotri, PhD, has long studied how the brain develops and what goes wrong in neurological disorders. For almost as long, he has also been curious about the evolution of the human brain -- what changed that makes us so different from preceding Neanderthals and Denisovans, our closest evolutionary relatives, now extinct?

 

Evolutionary studies rely heavily on two tools -- genetics and fossil analysis -- to explore how a species changes over time. But neither approach can reveal much about brain development and function because brains do not fossilize, Muotri said. There is no physical record to study.

 

So Muotri decided to try stem cells, a tool not often applied in evolutionary reconstructions. Stem cells, the self-renewing precursors of other cell types, can be used to build brain organoids -- "mini brains" in a laboratory dish. Muotri and colleagues have pioneered the use of stem cells to compare humans to other primates, such as chimpanzees and bonobos, but until now a comparison with extinct species was not thought possible.

 

In a study published February 11, 2021 in Science, Muotri's team catalogued the differences between the genomes of diverse modern human populations and the Neanderthals and Denisovans, who lived during the Pleistocene Epoch, approximately 2.6 million to 11,700 years ago. Mimicking an alteration they found in one gene, the researchers used stem cells to engineer "Neanderthal-ized" brain organoids.

 

"It's fascinating to see that a single base-pair alteration in human DNA can change how the brain is wired," said Muotri, senior author of the study and director of the UC San Diego Stem Cell Program and a member of the Sanford Consortium for Regenerative Medicine. "We don't know exactly how and when in our evolutionary history that change occurred. But it seems to be significant, and could help explain some of our modern capabilities in social behavior, language, adaptation, creativity and use of technology."

 

The team initially found 61 genes that differed between modern humans and our extinct relatives. One of these altered genes -- NOVA1 -- caught Muotri's attention because it's a master gene regulator, influencing many other genes during early brain development. The researchers used CRISPR gene editing to engineer modern human stem cells with the Neanderthal-like mutation in NOVA1. Then they coaxed the stem cells into forming brain cells and ultimately Neanderthal-ized brain organoids.

 

Brain organoids are little clusters of brain cells formed by stem cells, but they aren't exactly brains (for one, they lack connections to other organ systems, such as blood vessels). Yet organoids are useful models for studying genetics, disease development and responses to infections and therapeutic drugs. Muotri's team has even optimized the brain organoid-building process to achieve organized electrical oscillatory waves similar to those produced by the human brain.

 

The Neanderthal-ized brain organoids looked very different than modern human brain organoids, even to the naked eye. They had a distinctly different shape. Peering deeper, the team found that modern and Neanderthal-ized brain organoids also differ in the way their cells proliferate and how their synapses -- the connections between neurons -- form. Even the proteins involved in synapses differed. And electrical impulses displayed higher activity at earlier stages, but didn't synchronize in networks in Neanderthal-ized brain organoids.

 

According to Muotri, the neural network changes in Neanderthal-ized brain organoids parallel the way newborn non-human primates acquire new abilities more rapidly than human newborns.

"This study focused on only one gene that differed between modern humans and our extinct relatives. Next we want to take a look at the other 60 genes, and what happens when each, or a combination of two or more, are altered," Muotri said.

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March 6, 2021 2:56 PM
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Origin of life: The chicken-and-egg problem

Origin of life: The chicken-and-egg problem | Amazing Science | Scoop.it

New research shows that slight alterations in transfer-RNA molecules (tRNAs) allow them to self-assemble into a functional unit that can replicate information exponentially. tRNAs are key elements in the evolution of early life-forms.

 

A Ludwig-Maximilians-Universitaet (LMU) in Munich team has shown that slight alterations in transfer-RNA molecules (tRNAs) allow them to self-assemble into a functional unit that can replicate information exponentially. tRNAs are key elements in the evolution of early life-forms.

 

Life as we know it is based on a complex network of interactions, which take place at microscopic scales in biological cells, and involve thousands of distinct molecular species. In our bodies, one fundamental process is repeated countless times every day. In an operation known as replication, proteins duplicate the genetic information encoded in the DNA molecules stored in the cell nucleus -- before distributing them equally to the two daughter cells during cell division. The information is then selectively copied ('transcribed') into what are called messenger RNA molecules (mRNAs), which direct the synthesis of the many different proteins required by the cell type concerned. A second type of RNA -- transfer RNA (tRNA) -- plays a central role in the 'translation' of mRNAs into proteins. Transfer RNAs act as intermediaries between mRNAs and proteins: they ensure that the amino-acid subunits of which each particular protein consists are put together in the sequence specified by the corresponding mRNA.

 

How could such a complex interplay between DNA replication and the translation of mRNAs into proteins have arisen when living systems first evolved on the early Earth? We have here a classical example of the chicken-and-the-egg problem: Proteins are required for transcription of the genetic information, but their synthesis itself depends on transcription.

 

LMU physicists led by Professor Dieter Braun have now demonstrated how this conundrum could have been resolved. They have shown that minor modifications in the structures of modern tRNA molecules permit them to autonomously interact to form a kind of replication module, which is capable of exponentially replicating information. This finding implies that tRNAs -- the key intermediaries between transcription and translation in modern cells -- could also have been the crucial link between replication and translation in the earliest living systems. It could therefore provide a neat solution to the question of which came first -- genetic information or proteins?

 

Strikingly, in terms of their sequences and overall structure, tRNAs are highly conserved in all three domains of life, i.e. the unicellular Archaea and Bacteria (which lack a cell nucleus) and the Eukaryota (organisms whose cells contain a true nucleus). This fact in itself suggests that tRNAs are among the most ancient molecules in the biosphere.

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Scooped by Dr. Stefan Gruenwald
March 5, 2021 1:16 PM
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Fighting shingles with nanoviricides

Fighting shingles with nanoviricides | Amazing Science | Scoop.it

The company NanoViricides, Inc. is taking a unique approach to fighting herpes (shingles) and other viral infections by using tiny decoys, termed nanoviricides, to bind and inactivate the virus.

 

Nanoviricides are composed of micelles with up to 1,200 chemically attached ligands on their surface. These ligands mimic the cellular receptors targeted by the relevant virus or class of virus. When a virion is bound by a nanoviricide via the virion’s cell-receptor-binding glycoproteins, the lipid envelope of the virus merges with the lipids attached to the nanoviricide. This lipid mixing destabilizes the virion, rendering it incapable of infecting host cells.

 

NanoViricides’ shingles drug candidate is moving rapidly toward the clinic as a topical treatment for shingles. The company also has related drug candidates with follow-on applications against other herpes infections in its HerpeCide program.

 

According to Anil R. Diwan, NanoViricides’ president and chairman, “our anti-herpes drug development program has produced impressive results in animal models and, with limited additional testing, we are close to declaring a drug candidate that will move into clinical testing.”

 

Indeed, a nanoviricide against HSV-1 has shown impressive activity in mice, providing proof of concept for the success of similar drugs in humans. Because nanoviricides attack viruses directly, the host environment is not expected to affect their activity. In experiments performed in the laboratory of Ken Rosenthal at Northeast Ohio Medical University, mice were infected with the highly virulent H129c strain of HSV-1, which is uniformly fatal. However, in mice treated with an anti-herpes nanoviricide, viral load dropped by 99.9%, lesion progression was halted, and >85% of the mice survived.

george sperco's curator insight, February 7, 2023 1:53 PM
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