Genome editing, i.e. the ability to mutagenize, insert, delete and replace sequences, in living cells is a powerful and highly desirable method that could potentially revolutionize plant basic research and applied biotechnology. Indeed, various research groups from academia and industry are in a race to devise methods and develop tools that will enable not only site-specific mutagenesis but also controlled foreign DNA integration and replacement of native and transgene sequences by foreign DNA, in living plant cells. In recent years, much of the progress seen in gene targeting in plant cells has been attributed to the development of zinc finger nucleases and other novel restriction enzymes for use as molecular DNA scissors. The induction of double-strand breaks at specific genomic locations by zinc finger nucleases and other novel restriction enzymes results in a wide variety of genetic changes, which range from gene addition to the replacement, deletion and site-specific mutagenesis of endogenous and heterologous genes in living plant cells. In this review, we discuss the principles and tools for restriction enzyme-mediated gene targeting in plant cells, as well as their current and prospective use for gene targeting in model and crop plants.
Melanoma drug On 4 September, US regulators issued their first approval of a drug that helps the immune system to fight cancer by blocking a protein called PD-1 (see Nature 508, 24–26; 2014). The drug, Keytruda (pembrolizumab), made by Merck of Whitehouse Station, New Jersey, was granted accelerated approval by the US Food and Drug Administration for patients with advanced melanoma that does not respond to other treatments. Merck plans to charge about US$12,500 for a month’s supply of Keytruda.
Ed Rybicki's insight:
"...plans to charge about US$12,500 for a month’s supply of Keytruda."
Sounds like a candidate for plant expression to me!
While healthy people have proteins in their blood called clotting factors that act quickly to plug wounds, hemophiliacs lack these proteins, making even minor bleeds difficult to stop.
The main treatment option for people with severe hemophilia is to receive regular infusions of clotting factor. But 20 to 30 percent of people who get these infusions develop antibodies, called inhibitors, against the clotting factor. Once these inhibitors develop, it can be very difficult to treat or prevent future bleeding episodes.
In a new study, researchers from the University of Pennsylvania School of Dental Medicine and theUniversity of Florida College of Medicine teamed up to develop a strategy to prevent these antibodies from forming. Their approach, which uses plant cells to teach the immune system to tolerate rather than attack the clotting factor protein, offers hope for preventing one of the most serious complications of hemophilia treatment.
With the Ebola outbreak threatening to spiral out of control, U.S. officials unveiled a multimillion-dollar plan Tuesday aimed at getting a promising drug out of American research labs and into African hospitals and clinics more quickly.
Ed Rybicki's insight:
They didn't use my quote about mainlining green juice if it would save my life - but that's OK B-)
Will the public swallow science’s best solution to one of the most dangerous wheat pathogens on the planet?
Some wheat varieties are resistant to Ug99, but they represent just 10 percent of the varieties grown around the world. And even these plants are not necessarily immune to infection. Ug99 continues to mutate and spread, and new virulent races, or biotypes, of the fungus that are able to skirt plant resistance strategies could emerge at any time. Just last year, for example, outbreaks of a novel stem rust race in Ethiopia and Germany infected Ug99-resistant wheat plants. In the oft-repeated words of the late wheat-breeding pioneer Norman Borlaug of the Rockefeller Foundation and CIMMYT, “Rust never sleeps.”
Most wheat researchers and breeders agree that to protect plants from Ug99, they must develop wheat varieties with several rust-resistance genes, so that if the fungus mutates to outwit one defense, there are others there to take on the pathogen. The problem is that it can take years to achieve this goal using traditional breeding methods. In the meantime, favorable winds could spread Ug99 even farther, and the fungus continues to evolve resistance to wheat crops’ natural defenses.
One way to hasten the development of a long-lasting stem rust–resistant wheat variety is to engineer plants’ DNA to carry resistance genes, creating what are known as genetically modified (GM) crops. But at many of the facilities that develop wheat varieties—primarily led by academic breeding groups, in contrast to the commercial domination of corn and soybean development—such transgenic approaches are taboo, as public opposition, regulatory expenses, and genetic complexity have kept wheat transgenics off the market. “We could do millions of things [with transgenics],” says Jorge Dubcovsky, a wheat geneticist and breeder at the University of California, Davis, “but we have our hands tied.”
Ed Rybicki's insight:
The question should rather be: "Want wheat? Yes? GMO or nothing, baby...".
Seriously: without some imaginative engineering, wheat rusts may yet get the better of one of humanity's favourite crops.
Giving ZMapp, a cocktail of antibodies, to rhesus macaques up to five days after infection with the Ebola virus completely protected the animals — a finding that a Canadian-led research team says supports use of the treatment during the current outbreak in West Africa.
Biopharmed drugs offer much promise; but how should they be regulated?
Using genetic engineering in plants to create biopharmed drugs holds all sorts of promise for treating diseases, as the recent case of a drug which appears to have cured two Ebola patients has shown, but regulators may be holding this field back, argues Henry Miller in a Wall Street Journal op-ed.
Biopharming involves genetically engineering crops such as corn, tomato, and tobacco to create high concentrations of antibodies and other pharmaceuticals that can then be harvested.
The drug used in the two US Ebola patients, called ZMapp, is one of these; a mixture of three antibodies taken from tobacco plants that were infected with engineered plant viruses. These kinds of drugs have such "great potential," Miller says, because the raw materials are cheap and they can be scaled up far more cheaply than bricks-and-mortar factories. That fluid scalability enables drug firms to hold off on investing in production facilities until later in the clinical testing cycle, or until the market it will target can be better estimated.
Sandusky Register Ebola puts focus on tobacco plant use The Durango Herald Biotech greenhouse associate specialist Derek Haynes replaces young tobacco plants of a unique strain in the greenhouse at Medicago USA, Inc.
ICON GENETICS is a provider of new plant engineering technologies which address precision, speed, expression control and safety of transgene management in plants. We develop platforms and product prototypes for pharmaceutical, animal health and chemical biotech markets. ICON's Intellectual Property portfolio provides broad freedom-to-operate for all major expression systems, including nuclear transformation, plastid transformation, and transient expression based on pro-viral vectors. ICON's products consist of technology suites with emphasis on transient expression and designer glycosylation, and apipeline of biopharmaceuticals in development.
NHL Vaccine in Phase I
Icon Genetics successfully completes Phase I clinical study with personalized vaccines for treatment of non-Hodgkin's lymphoma,Jan`14
Kentucky Bioprocessing, Icon Genetics and Mapp Biopharmaceutical have entered into discussions to merge their businesses,May`12
We report the successful use of TALENs under the control of an estrogen-inducible promoter for targeted mutagenesis in tomato (Solanum lycopersicum) of the negative regulator of gibberellin signaling PROCERA(PRO). TALEN expression was induced and plants were regenerated from cotyledons of seedlings derived from stable transgenic lines. Six of 40 regenerated plants carried pro alleles, and the mutations in the two lines examined were heritable. Homozygous pro segregants exhibited phenotypes consistent with increased gibberellin response.
The body is structured to ensure that any invading organisms have a tough time reaching the brain, an organ obviously critical to survival. Known as the blood-brain barrier, cells that line the brain and spinal cord are tightly packed, making it difficult for anything besides very small molecules to cross from the bloodstream into the central nervous system. While beneficial, this blockade also stands in the way of delivering drugs intended to treat neurological disorders, such as Alzheimer’s.
In a new study published in the journal Molecular Therapy, University of Pennsylvania researchers have found a way of traversing the blood-brain barrier, as well as a similar physiological obstacle in the eye, the retinal-blood barrier. By pairing a receptor that targets neurons with a molecule that degrades the main component of Alzheimer’s plaques, the biologists were able to substantially dissolve these plaques in mice brains and human brain tissue, offering a potential mechanism for treating the debilitating disease, as well as other conditions that involve either the brain or the eyes.
This talk was given at a local TEDx event, produced independently of the TED Conferences. Ed explores new ways to make pharmaceuticals inexpensive and asks: ...
A team of virologists and plant geneticists at Wageningen UR has demonstrated that when tomato plants contain Ty-1 resistance to the important Tomato yellow leaf curl virus (TYLCV), parts of the virus DNA (the genome) become hyper-methylated, the result being that virus replication and transcription is inhibited. The team has also shown that this resistance has its Achilles heel: if a plant is simultaneously infected with another important (RNA) virus, the Cucumber mosaic virus (CMV), the resistance mechanism is compromised.
Ed Rybicki's insight:
...first heard of by us just the other day, when Richard Kormelink of Wageningen gave the Biopharming Research Unit a seminar! Really good work
•Current phylogenetic data do not support the existence of IAA biosynthesis in algae.•Plant Trp-dependent IAA biosynthesis has been shaped by gene transfer.•IAA biosynthesis in plants evolved in response to microbe–plant interactions.
The recent finding of the tryptophan aminotransferase (TAA)/flavin monooxygenase (YUC) pathway as the principal route of auxin production in plants provides an opportunity to revisit the origin of plant auxin biosynthesis. Phylogenetic analyses of the TAA and YUC gene families provide very little evidence for the production of indole-3-acetic acid (IAA) in algae. Instead, horizontal gene transfer of YUCs from bacteria to the ancestral land plant suggests that the TAA/YUC pathway is a land plant innovation. In this Opinion article we postulate that the origin of tryptophan-dependent IAA biosynthesis in land plants might have evolved in response to interactions with microbes, particularly bacteria, allowing plants to counteract bacterial activities and control their own auxin signaling.
A Liberian health worker who recovered from Ebola after receiving an experimental drug is urging the manufacturer to speed up its production and send it to Africa,
Two Ebola patients, given the experimental drug ZMapp, have been allowed to leave a treatment centre in the Liberian capital after testing negative for the disease. The pair – both medics – were greeted by country’s president in Monrovia.
“Really, really good news. First of all I just want to say to both of you, how happy we are that you have survived this,” said Ellen Johnson Sirleaf.
Meanwhile, residents have been celebrating the lifting of a blockade in a neighbourhood of the capital.
Streets in the West Point district had been closed for 10 days after an Ebola health centre was stormed.
Residents had feared that they would run out of food and safe water due to the outbreak.
In Sierra Leone, youth groups have taken to the streets of Freetown to raise awareness of Ebola, as the virus continues to spread.
More than three thousand cases have now been reported across West Africa.
Liberia has been the hardest hit, reporting at least 694 deaths.
Senegal has joined the list of affected countries, announcing its first case on Friday.
MONROVIA, August 25- A Liberian doctor treated with experimental American anti-Ebola serum ZMapp has died, the west African nation said on Monday. Abraham Borbor
A Bioengineered Glow-in-the-Dark Plant Is Your Next Night Light Motherboard That's why you could soon find yourself reading a bedtime book by the soft green light of a glow-in-the-dark plant.
PlantForm Corporation is a Canadian company with an ultra-low-cost solution. We use plants to produce monoclonal antibodies, protein drugs and vaccines – for as little as one-tenth of the manufacturing cost of other biopharmaceutical production systems.
Our pipeline includes:
three biosimilar drugs for oncology, leading with biosimilar Herceptin® (trastuzumab) for breast cancerinnovator antibodies to fight HIV/AIDSrecombinant butyrylcholinesterase to provide prophylactic protection against nerve agents
iBio, Inc. (IBIO:AMEX), a leader in the plant-made pharmaceutical field, develops and offers pharmaceutical product applications using its iBioLaunch™ platform. The iBioLaunch platform is a proprietary, transformative technology for the production of biologics including monoclonal antibodies, other therapeutic proteins and vaccines. It uses proprietary, transient gene expression in unmodified green plants instead of materials such as chicken eggs, bacteria, mammalian and insect cells, transgenic plants, and human blood plasma required by other systems, to produce important biologic pharmaceuticals. This unique plant-based platform offers a number of significant advantages over other systems:
Ability to synthesize complex proteins at which other systems have failedSimplicity, scalability and flexibilityReduced capital investmentLower operating costsSurge capacityRapid production times – gene sequence to factory-scale protein harvestEliminates the need of bioreactorsLow risk of contamination by animal pathogens
iBio has a strong IP/technology portfolio and has been well established by more than nine years of applications development and $100 million in funding. Our current pipeline includes:
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