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Scooped by
Gerd Moe-Behrens
December 5, 2012 2:27 PM
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By Caroline Arbanas "Our bodies contain far more microbial genes than human genes. And a new study suggests that just as human DNA varies from person to person, so too does the massive collection of microbial DNA in the intestine. The research is the first to catalog the genetic variation of microbes that live in the gut, where they extract nutrients from food, synthesize vitamins, protect against infections, and produce compounds that naturally reduce inflammation. The widespread genetic diversity uncovered by the scientists can help them understand how our microbial genes work together with our human genes to keep us healthy or, in some cases, to cause disease."
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Scooped by
Gerd Moe-Behrens
December 5, 2012 6:30 AM
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by Newcomb CJ, Moyer TJ, Lee SS, Stupp SI. "Elucidating the structural information of nanoscale materials in their solvent-exposed state is crucial, as a result, cryogenic transmission electron microscopy (cryo-TEM) has become an increasingly popular technique in the materials science, chemistry, and biology communities. Cryo-TEM provides a method to directly visualize the specimen structure in a solution-state through a thin film of vitrified solvent. This technique complements X-ray, neutron, and light scattering methods that probe the statistical average of all species present; furthermore, cryo-TEM can be used to observe changes in structure over time. In the area of self-assembly, this tool has been particularly powerful for the characterization of natural and synthetic small molecule assemblies, as well as hybrid organic-inorganic composites. In this review, we discuss recent advances in cryogenic TEM in the context of self-assembling systems with emphasis on characterization of transitions observed in response to external stimuli." http://1.usa.gov/THmWkD
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Rescooped by
Gerd Moe-Behrens
from GenoCon 2
December 4, 2012 1:39 PM
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New Submission Date Friday January 18th 2013 GenoCon2 Design Challenge A is officially launched! The challenge is to design a synthetic Arabidopsis promoter system of 500 base-pairs (or less) for selectively controlling the expression of a gene. These 500 base-pairs must be consecutive, and within the region prescribed by the GenoCon genetic vector and measurement assay system. Solutions may (1) localize gene expression to specific plant tissues such as the leaves, shoots, or wounds, (2) control the time of gene expression such as in plant senescence and circadian regulation, or may use a combination of both approaches. http://genocon.org/assignment-2012/assignment-a/background-2012/
Via David Gifford
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Scooped by
Gerd Moe-Behrens
December 3, 2012 4:16 PM
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A new genomics research center sits at the nexus of medicine, science, engineering and the humanities. The goal is nothing short of improving human well-being.
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Scooped by
Gerd Moe-Behrens
December 3, 2012 1:17 PM
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by U. TORONTO "It looks like a smiley face tattoo, but a new easy-to-apply sensor can detect medical problems and help athletes fine-tune training routines.“We wanted a design that could conceal the electrodes,” says Vinci Hung, a PhD candidate in physical and environmental sciences at the University of Toronto, who helped create the new sensor. “We also wanted to showcase the variety of designs that can be accomplished with this fabrication technique.” The tattoo, which is an ion-selective electrode (ISE), is made using standard screen printing technique and commercially available transfer tattoo paper—the same kind of paper that usually carries tattoos of Spiderman or Disney princesses. In the case of the sensor, the “eyes” function as the working and reference electrodes, and the “ears” are contacts for a measurement device to connect to. Hung contributed to the work while in the lab of Joseph Wang, a professor at the University of California, San Diego. The sensor she helped make can detect changes in the skin’s pH levels in response to metabolic stress from exertion...." http://bit.ly/R1Gfa5
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Scooped by
Gerd Moe-Behrens
December 2, 2012 4:40 PM
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Origins of Synthetic Biology
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Scooped by
Gerd Moe-Behrens
December 1, 2012 2:04 PM
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"Design could create a DNA molecule that is far better*....? Aesthetics in synthesis and synthetic biology http://bit.ly/Xcbl0r
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Scooped by
Gerd Moe-Behrens
December 1, 2012 11:50 AM
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by Anne Trafton "Borrowing from microfabrication techniques used in the semiconductor industry, MIT and Harvard Medical School (HMS) engineers have developed a simple and inexpensive way to create three-dimensional brain tissues in a lab dish. The new technique yields tissue constructs that closely mimic the cellular composition of those in the living brain, allowing scientists to study how neurons form connections and to predict how cells from individual patients might respond to different drugs. The work also paves the way for developing bioengineered implants to replace damaged tissue for organ systems, according to the researchers. “We think that by bringing this kind of control and manipulation into neurobiology, we can investigate many different directions,” says Utkan Demirci, an assistant professor in the Harvard-MIT Division of Health Sciences and Technology...." http://bit.ly/YBl1BW
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Scooped by
Gerd Moe-Behrens
November 30, 2012 5:44 PM
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(Phys.org)—While some advanced humanoid robots already look eerily lifelike, robots in the future may actually become partly alive.
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Scooped by
Gerd Moe-Behrens
November 30, 2012 5:11 PM
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by Yonggang Ke, Luvena L. Ong, William M. Shih, and Peng Yin "We describe a simple and robust method to construct complex three-dimensional (3D) structures by using short synthetic DNA strands that we call “DNA bricks.” In one-step annealing reactions, bricks with hundreds of distinct sequences self-assemble into prescribed 3D shapes. Each 32-nucleotide brick is a modular component; it binds to four local neighbors and can be removed or added independently. Each 8–base pair interaction between bricks defines a voxel with dimensions of 2.5 by 2.5 by 2.7 nanometers, and a master brick collection defines a “molecular canvas” with dimensions of 10 by 10 by 10 voxels. By selecting subsets of bricks from this canvas, we constructed a panel of 102 distinct shapes exhibiting sophisticated surface features, as well as intricate interior cavities and tunnels." http://bit.ly/QTt23i
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Scooped by
Gerd Moe-Behrens
November 30, 2012 12:00 PM
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Brain without a body "A computationally advanced, million-neuron model of the brain successfully demonstrates perception, cognition, and behavior. " A Large-Scale Model of the Functioning Brain by Chris Eliasmith, Terrence C. Stewart, Xuan Choo, Trevor Bekolay, Travis DeWolf, Charlie Tang, Daniel Rasmussen "A central challenge for cognitive and systems neuroscience is to relate the incredibly complex behavior of animals to the equally complex activity of their brains. Recently described, large-scale neural models have not bridged this gap between neural activity and biological function. In this work, we present a 2.5-million-neuron model of the brain (called “Spaun”) that bridges this gap by exhibiting many different behaviors. The model is presented only with visual image sequences, and it draws all of its responses with a physically modeled arm. Although simplified, the model captures many aspects of neuroanatomy, neurophysiology, and psychological behavior, which we demonstrate via eight diverse tasks." http://bit.ly/TwWRBX see comment Building the Human Brain by Christian K. Machens "The human brain is exceedingly complex and studying it encompasses gathering information across a range of levels, from molecular processes to behavior. The sheer breadth of this undertaking has perhaps led to an increased specialization of brain research and a concomitant fragmentation of our knowledge. A potential solution is to integrate all of this knowledge into a coherent simulation of the brain (1). However, simply “building” a brain from the bottom up by replicating its parts, connections, and organization fails to capture its essential function—complex behavior (2). Instead, just as engineers can only construct cars and computers because they know how they work, we will only be able to construct a brain if we know how it works—that is, if we understand the computations that are carried out in individual brain areas, and how these computations are implemented on the level of neural networks. On page 1202 of this issue, Eliasmith et al. (3) make headway toward this benchmark by presenting just such a large-scale computational model of the human brain that can simulate a variety of complex behaviors." http://bit.ly/U6CFGa
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Scooped by
Gerd Moe-Behrens
November 30, 2012 11:16 AM
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Standard European Vector Architecture (SEVA) platform is a web-based resource and a material clone repository http://bit.ly/SkmVSu
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Scooped by
Gerd Moe-Behrens
November 30, 2012 10:29 AM
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Scooped by
Gerd Moe-Behrens
December 5, 2012 10:30 AM
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By Mikey Campbell "The brainchild of photographer and author Rick Smolan, "The Human Face of Big Data" app offers a well-curated collection of tantalizing essays and photographs delving into Big Data, a revolution in information and analytics that is changing the very world we live in." http://bit.ly/VmtD91
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Scooped by
Gerd Moe-Behrens
December 4, 2012 1:50 PM
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Biological Pathways and the Semantic Web... WikiPathways (www.wikipathways.org) is a community-driven pathway resource [1-3]. It is inspired by Wikipedia and aims at capturing knowledge about biological pathways in such a way that it can be used for data analysis. For the Innovative Medicine Initiative project Open PHACTS [4], we expose the contents of WikiPathways in semantic web format. We are taking a multi-pronged approach, selecting different ontologies to capture diverse aspects of semantics. As an established pathway ontology, BioPAX [5] forms the bulk of the semantics for the actual pathway content, but we also use other specialized ontologies to capture the semantics of curators, authors, and other WikiPathways-specific meta data.
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Scooped by
Gerd Moe-Behrens
December 4, 2012 1:36 PM
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By Jeffrey M. Perkel "James DiCarlo was only a freshman at Johns Hopkins University in the spring of 2007 when his research advisor, Jef Boeke, approached him about taking a new class Boeke was putting together. “Do you think students would be interested in a class about synthetic biology and building genomes?” DiCarlo recalls Boeke asking. “I was like, ‘Yeah, that sounds awesome, I would take that class,’” DiCarlo, now a grad student in biomedical engineering at Boston University, recalls. That class was Biology 420, aka Build-a-Genome. Instead of concentrating on typical cookbook-style experiments, Build-a-Genome teaches undergrads the fine points of synthetic biology and then turns them loose to rebuild their own 10-kilobase slice of yeast chromosome three. The course, a kind of lab class–cum-independent project, was conceived as part of an international yeast genome engineering research consortium called Sc2.0...." http://bit.ly/11yHfo0
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Scooped by
Gerd Moe-Behrens
December 3, 2012 3:07 PM
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"Computer scientists prove that networks of cells can compute as efficiently as networks of computers linked via the internet Distributed computing is all the rage these days. The idea is to break down computational tasks into convenient chunks and distribute them across a network to a number of computers. The benefits are clear, such as easy, on-demand access to huge computing resources. The conventional way to think about these systems is as independent Turing machines connected by a network that allows them to exchange large messages. This so-called ‘message passing model’ certainly applies to much of the distributed computing that takes place on the internet; projects such as the SETI@home and the Einstein @home programs. But there is a growing awareness that many networks are much more limited, both in the size of the messages they can transmit and receive and also in the processing capacity at each node. A biological cell, for example, can transmit and receive only limited amounts of information and can perform only rudimentary processing tasks. It’s easy to imagine that a network of cells can perform only very simple distributed computing tasks. On the other hand, perhaps they can make up for their individual deficiencies by working as a group and so are just as capable as other networks. So an important question is how these limitations influence the classes of distributed computing tasks that groups of cells can perform. Today we have an answer thanks to the work of Yuval Emek, Jasmin Smula and Roger Wattenhofer at the Swiss Federal Institute of Technology in Zurich. “We believe that there is a need for a network model, where nodes are by design below the computation and communication capabilities of Turing machines,” they say. These guys have modelled the computing behaviour of a network of these sub-Turing machines, which they call finite state machines. They show that far from being critically handicapped, a network of finite state machines is capable of solving many of the standard problems in conventional distributed computing, such as the 3-colouring of undirected trees . What’s more, these networks can do the job just as efficiently–in a time that is poly-logarithmic with the number of cells. That could turn out to have far reaching consequences. It may be a stretch to imagine a network of cells joining the SETI@home project. But it provides a framework in which to study how networks of cells might solve other common problems in biological systems such as forward planning, trajectory calculations and so on. The new model can also be applied in more prosaic ways, such as predicting the performance of networks of sensors which are strongly constricted by power limitations. Emek and co ask the question: “do tiny bio/nano nodes “compute” and/or “communicate” essentially [in] the same [way] as a computer?” The answer, it would seem, is yes, which means it is an exciting time to be a distributed computing specialist working in biology." http://bit.ly/11sDwIA
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Scooped by
Gerd Moe-Behrens
December 2, 2012 4:51 PM
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by Allison McCann "Synthetic biology, the newer, cooler branch of genetic engineering, has gained a lot of attention in recent years because of its innovative take on biology, as well as for its similarities with the hugely successful software industry. But synthetic biology still struggles in one key area where the software industry excels: open access to information. Synthetic biology could easily be buried beneath patents protecting proprietary information, much like the pharmaceutical and biotech industries today. And while computer science and synthetic biology aren’t identical (there will likely be a lot less on the consumer-facing end from engineered DNA), a more open-source model within synthetic biology could expedite the experimentation process, allowing researchers to focus on the engineering aspects and not time-consuming DNA synthesis — ultimately bringing some of these ungodly sounding new life-forms out from labs and into the commercial world." http://bit.ly/YFcSwe
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Scooped by
Gerd Moe-Behrens
December 1, 2012 3:33 PM
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Fifty-nine years after James Watson and Francis Crick deduced the double-helix structure of DNA, a scientist has captured the first direct photograph of the twisted ladder that props up life.
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Scooped by
Gerd Moe-Behrens
December 1, 2012 1:30 PM
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Scooped by
Gerd Moe-Behrens
November 30, 2012 5:46 PM
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Manipulation of signal transduction pathways presents a viable mechanism to interface cells with electronics. In this work, we present a two-step signal transduction pathway involving cellular and electronic transduction elements.
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Scooped by
Gerd Moe-Behrens
November 30, 2012 5:17 PM
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"Researchers at the Wyss Institute for Biologically Inspired Engineering at Harvard University have created more than 100 three-dimensional (3D) nanostructures using DNA building blocks that function like Lego® bricks — a major advance from the two-dimensional (2D) structures the same team built a few months ago." http://bit.ly/11sbNa3
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Scooped by
Gerd Moe-Behrens
November 30, 2012 5:03 PM
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by Kurt V. Gothelf "Parallels are often drawn between the construction of molecular structures and building toy models in LEGO bricks. This analogy is particularly suitable for the method reported by Ke et al. on page 1177 of this issue (1). The authors describe the construction of arbitrary and discrete three-dimensional (3D) DNA structures by self-assembly of single-stranded DNA “bricks.” The method opens a new route to complex self-assembled (3D) nanostructures that may serve as addressable templates for placing guest molecules with high precision, with possible applications in biophysics, medicine, and nanoelectronics." http://bit.ly/YyTq4t
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Scooped by
Gerd Moe-Behrens
November 30, 2012 11:50 AM
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Curiosity drives humanity. When confronted with a new phenomenon, we are compelled to search for understanding. We can then control the science with new technologies, making life easier.
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Scooped by
Gerd Moe-Behrens
November 30, 2012 10:50 AM
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Iterative plug-and-play methodology for constructing and modifying synthetic gene networks
by Kevin D Litcofsky, Raffi B Afeyan, Russell J Krom, Ahmad S Khalil & James J Collins "We present a methodology for the design, construction and modification of synthetic gene networks. This method emphasizes post-assembly modification of constructs based on network behavior, thus facilitating iterative design strategies and rapid tuning and repurposing of gene networks. The ease of post-construction modification afforded by this approach and the ever-increasing repository of components within the framework will help accelerate the development of functional genetic circuits for synthetic biology." http://bit.ly/Twa4vp A free PDF from the Collins lab can be found here: http://www.bu.edu/abl/files/naturemethods_litcofsky.pdf
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