New research yields insights into Parkinson's disease

Researchers at the University of Toronto Scarborough (UTSC) used an innovative technique to examine chemical interactions that are implicated in Parkinson's Disease.

The work details how a protein called alpha-synuclein interacting with the brain chemical dopamine can lead to protein misfolding and neuronal death.

Parkinson's Disease is a neurodegenerative disease which results in loss of motor control and cognitive function. Although the cause isn't known precisely, the disease involves the death of brain cells that produce dopamine, a chemical important in neuronal signaling. The disease also involves a protein called alpha-synuclein which aggregates in the neurons of people with the disease.

Kagan Kerman, a chemist in the Department of Physical and Environmental Sciences, and Ian R. Brown, a neuroscientist who founded UTSC's Centre for the Neurobiology of Stress in the Department of Biological Sciences, looked at the way dopamine interacts with alpha-synuclein to form aggregates that may be toxic to neurons.

"This is very fundamental," says Kagan Kerman. "It gives us a new point of view of the misfolding proteins and how they are affected by dopamine."

These sorts of interactions are often studied using microscopy. But the UTSC researchers decided to use an electroanalytic technique called voltammetry. By studying tiny changes in electric current as dopamine and alpha-synuclein interacted they were able to determine details about the early phases of the interaction.

Using the technique, they were able to detail how changes in pH levels and ionic strength of the solution affected the interaction. They found that at higher pH levels and higher ionic strengths, dopamine interacted much more strongly with alpha-synuclein, forming aggregates more quickly.

The results could have implications for understanding and treating the disease. Normally dopamine is contained in structures called vesicles, in which pH levels are low and dopamine is unlikely to interact with alpha-synuclein. 

Outside of the vesicles dopamine encounters higher pH levels and, according to the new research, is much more likely to interact to create aggregates.

The analysis was done using chemicals deposited onto screen-printed electrodes only 12.5 mm by 4 mm. The electrodes were manufactured at Osaka University, where Kerman completed his PhD work. Because they are so small, the electrodes allowed analysis to be done on tiny samples.

The technique is a potentially quicker and cheaper way to study protein misfolding, and could be automated to screen drugs that might treat the disease, says Brown.

The research was published in Chemical Neuroscience, published by the American Chemical Society.

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New drug strategy attacks resistant leukemia and lymphoma

Scientists build a synthetic peptide that overcomes cancer cells' survival defenses
  

BOSTON--Scientists at the Dana-Farber/Children's Hospital Cancer Center have developed an anti-cancer peptide that overcomes the stubborn resistance to chemotherapy and radiation often encountered in certain blood cancers when the disease recurs following initial treatment.

The strategy could pave the way for much needed new therapies to treat relapsed and refractory blood cancers, which are difficult to cure because their cells deploy strong protein "deflector shields" to neutralize the cell death signals that chemotherapy agents used against them initially, say the researchers.

The prototype compound, called a "stapled BIM BH3 peptide," is designed to disable the cancer's defenses by hitting a family of protein targets that regulate cell death.

In proof-of-concept studies in mice with transplanted, drug-resistant leukemia tumors, the compound alone suppressed cancer growth, and when paired with other drugs, showed synergistic anti-cancer activity, say researchers led by Loren Walensky, MD, PhD, of Dana-Farber/Children's Hospital Cancer Center.

Their paper has been posted online by the Journal of Clinical Investigation and will appear in the journal's June issue. Walensky is the senior author and James LaBelle, MD, PhD, is the first author.

A cell's "fate" – when and whether it lives or dies – depends on a tug-of-war between pro-death and anti-death forces within the cell that serve as a check-and-balance system to maintain orderly growth. The system is regulated by the BCL-2 family of proteins, which contains both pro-death and pro-survival members.

When cells are no longer needed or are damaged beyond repair, the body activates pro-death BCL-2 proteins to shut down mitochondria – the power plants of the cell– resulting in an orchestrated cellular destruction known as apoptosis, or programmed cell death.

Many cell-killing cancer treatments work by triggering these "executioner proteins" to cause tumor cells to commit suicide in this fashion. But cancer cells can escape their death sentence – and even become immortal – by hyperactivating the survival arm of the family; these proteins intercept the executioner proteins and block their lethal mission.

"When cancers recur, they activate not just one type of survival protein, but many," explains Walensky, whose laboratory has extensively studied the cell-death system and makes compounds to manipulate it for research and therapeutic purposes.

"It's as if relapsed cancers 'learned' from their initial exposure to chemotherapy such that when they come back, they put up a variety of formidable barriers to apoptosis," he adds. "To reactivate cell death in refractory hematologic cancers, we need new pharmacologic strategies that broadly target these obstacles and substantially lower the apoptotic threshold."

When cancers specifically rely on one or two survival proteins, treating them with selective BCL-2 inhibitors can be very effective at eliminating the cancer cells' survival advantage. But relapsed cancers often evade such agents by deploying a battery of alternate survival proteins, so what's needed, Walensky says, are "next-generation" compounds that can block a wider range of survival proteins without jeopardizing normal tissues.

In the current research, the scientists built a chemically-reinforced peptide containing the death-activating BH3 domain of an especially potent killer protein, BIM, which is able to tightly bind with and neutralize all of the BCL-2 family survival proteins. This 'stapled' peptide, which incorporates the natural structure and properties of BIM BH3, not only disables the survival proteins, but also directly activates pro-death BCL-2 family proteins in cancer cells, making them self-destruct. Importantly, non-cancerous cells and tissues were relatively unaffected by the treatment.

"The diversity of BCL-2 family survival proteins blunts the anti-tumor activity of essentially all cancer treatments to some degree," Walensky points out. "By using Nature's solution to broad targeting of the BCL-2 pathway with a stapled BIM BH3 peptide, our goal is to eliminate cancer's protective force field and enable the arsenal of cancer treatments to do their job."

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Department of Biotechnology Announces A Pathbreaking Research:an International Consortium Sequences Tomato Genome

The Secretary, Department of Biotechnology Shri M K Bhan today announced a major leap forward in the field of Biotechnology Research. Mr. Bhan informed the media persons in New Delhi that the Tomato Genome Consortium (TGC), a group of over 300 scientists from fourteen countries, has sequenced the genomes of the domesticated tomato and its wild ancestor, Solanum pimpinellifolium. This achievement is expected to lower costs and speed up efforts to improve the worldwide tomato production, making it better equipped to combat the pests, pathogens, drought and diseases that now plague growers. The work may also speed up improvements in other crops. This important result is published in this week’s issue of Nature as cover story.

Main contributor Director of National Institute of Plant Genome Research Prof. Akhilesh Kumar Tyagi said that India contributed sequence of euchromatic region with emphasis on chromosome 5 of tomato and provided support to generate 5-fold sequence coverage of the entire tomato genome by Next Generation Sequence (NGS) technology. Indian Team also participated in performing annotation of all predicted proteins using international databases as a part of the International Tomato Annotation Group (ITAG). Simultaneously, Indian researchers have taken up analysis of specific genes/gene families related to ripening, nutrition, disease resistance and abiotic stress tolerance based on transcriptome data and comparative genomics. The genomic resources generated are expected to greatly accelerate improvement of tomato by functional genomics and molecular breeding. The University of Delhi South Campus (Principal Investigator- J.P. Khurana), National Research Centre on Plant Biotechnology, Indian Agricultural Research Institute (Principal Investigator- N.K. Singh), and National Institute of Plant Genome Research (Principal Investigator- D. Chattopadhyay), New Delhi, under the auspices of the Indian Initiative on Tomato Genome Sequencing (IITGS; Coordinator- A.K. Tyagi) participated in the international Tomato Genome Consortium (TGC). The Indian initiative was funded by the Department of Biotechnology, Government of India, and supported by the Indian Council for Agricultural Research.

Mr. Tyagi mentioned that the sequences provide a detailed overview at the functional portions of the tomato genome and its closest relative, revealing the order, orientation, types and relative positions of their 35,000 genes. The sequences will help researchers decipher the relationships between tomato genes and traits and broaden their understanding of genetic and environmental factors that interact to determine a field crop’s health and viability. Tomato is a member of the Solanaceae or nightshade family, and the new sequences are expected to provide reference points helpful for identifying important genes in tomato’s relatives. The group includes potato, pepper, eggplant and petunia and is the world’s most important vegetable plant family in terms of both economic value and production volume. Solanaceae members serve as sources of food, spices, medicines and ornamentals.

Elaborating further the Director of NIPGR Mr. Tyagi mentioned that the sequences also offer insight into how the tomato has diversified and adapted to new environments. They show that the tomato genome expanded abruptly about 60 million years ago, at a time close to one of the large mass extinctions. Subsequently, most of this genetic redundancy was lost. Some of the genes evolved during that event survive till today and control some of the most appealing traits of tomato.

Mr. Bhan said that the previous efforts have led to the sequencing of a number of other crop plants, including rice, corn, sorghum, poplar, potato, soybean, grape and Arabidopsis thaliana, a plant widely studied as a model organism. The availability of tomato genome sequence will not only serve as a reference for other Solanaceous species but also help in comparative genomics among diverse taxa.

TGC was established as a result of a scientific conference organized in 2003 in Washington, DC. Consortium members include scientists from Argentina, Belgium, China, France, Germany, India, Israel, Italy, Japan, Korea, Spain, the Netherlands, the United Kingdom and the United States.

The genome sequence and related resources can be accessed at the Solgenomics website
(http://solgenomics.net) and at http://mips.helmholtz-muenchen.de/plant/tomato/index.jsp

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Scientists decipher how T cells hunt down infection

T cells 'hunt' parasites like animal predators seek prey, study shows

By pairing an intimate knowledge of immune-system function with a deep understanding of statistical physics, a cross-disciplinary team at the University of Pennsylvania has arrived at a surprising finding: T cells use a movement strategy to track down parasites that is similar to strategies that predators such as monkeys, sharks and blue-fin tuna use to hunt their prey.

With this new insight into immune-cell movement patterns, scientists will be able to create more accurate models of immune-system function, which may, in turn, inform novel approaches to combat diseases from cancer to HIV/AIDS to arthritis.

The research involved a unique collaboration between the laboratories of senior authors Christopher Hunter, professor and chair of the Pathobiology Department in Penn's School of Veterinary Medicine, and Andrea Liu, the Hepburn Professor of Physics in the Department of Physics and Astronomy. Penn Vet postdoctoral researcher Tajie Harris and physics graduate student Edward Banigan also played leading roles in the research.

The study, which will be published in the journal Nature, was conducted in mice infected with the parasite Toxoplasma gondii. This single-celled pathogen is a common cause of infection in humans and animals; as much as a third of the world's population has a dormant form of this infection present in the brain. However, in immunocompromised individuals, such as those with HIV/AIDS or undergoing organ transplantation, this infection can have serious consequences, including brain inflammation and even death.

Earlier work had shown that T cells — a key immune-cell type — are central in preventing disease caused by T. gondii. In the new study, the Penn researchers used the infected mice as a natural model system to learn how the movement of T cells in the brain affects the body's ability to control this infection.

Among immunologists, it's widely believed that the movement of immune cells is governed in part by signaling proteins called chemokines. The Penn-led team demonstrated that a specific chemokine, CXCL10, and its receptor were abundantly produced in the brains of T. gondii-infected mice. When CXCL10 was blocked, mice had fewer T cells, a greater parasite burden and actively reproducing parasites.

Next the researchers sought to pinpoint the exact movement patterns of individual T cells in living tissue from T. gondii-infected mice. This was possible with multi-photon imaging, a technique that relies on a refined yet powerful microscope that can display living tissues in three dimensions in real time. Using this approach, the team found that CXCL10 appeared to play a role in the speed at which T cells are able to search for and control infection.To the extent that immunologists had considered T-cell movement patterns at all, many assumed that they moved in a highly directed fashion to find infected cells. But when the researchers analyzed the movement of T cells, they found their data did not match what would be expected: the T cells showed no directed motion.

That's where the statistical physics expertise of Liu and Banigan came in.

"We looked at a much more complete way to quantify these tracks and found that the standard model didn't fit at all," Liu said. "After some work we managed to find a model that did fit the tracks beautifully."

"The model that finally led us down the right path," Banigan said, "had a strong signature of something really interesting," a model known as a Lévy walk.

This "walk," or a mathematically characterized path, tends to have many short "steps" and occasional long "runs." The model was not fully consistent with the data, however.

"Rather, I had to look at variations on the Lévy walk model," Banigan said, because the researchers also observed that the T cells paused between steps and runs. Like the movements of the cells, the pauses were usually short but occasionally long.

Hunter likened the model to a strategy a person might employ to find misplaced keys in the house.

"When you lose your keys, how do you go about looking for them? You look in one place for a while, then move to another place and look there," he said.

"What that leads to is a much more efficient way of finding things," Liu said.

And, indeed, when the team modeled the generalized Lévy strategy against other strategies, they confirmed that the Lévy walk was a more efficient technique to find rare targets. That makes sense for T cells, which have to locate sparsely distributed parasites in a sea of mostly normal tissue.

Interestingly, T cells are not alone in employing a Lévy-type strategy to find their targets. Several animal predators move in a similar way — with many short-distance movements interspersed with occasional longer-distance moves — to find their prey. The strategy seems particularly common among marine predators, including tuna, sharks, zooplankton, sea turtles and penguins, though terrestrial species like spider monkeys and honeybees may use the same approach to locate rare resources.

This parallel with animal predators also makes sense because parasites, like prey species, have evolved to evade detection.

"Many pathogens know how to hide, so T cells are not able to move directly to their target," Hunter said. "The T cell actually needs to go into an area and then see if there's anything there."

The model is also relevant to cancer and other immune-mediated diseases, Hunter noted.

"Instead of looking for a parasite, these T cells could be looking for a cancer cell," he said. By knowing what controls T cell movement, "you might be able to devise strategies to make the T cells more efficient at finding those cells."

On the physics side, while the Lévy-walk model is not new, the fact that T cells pause in between their steps or runs is something that hadn't been recognized before when mapping the paths in other contexts.

"From a physics point of view, to have runs and pauses is a new model," Liu said. "Biological phenomena can illustrate what we wouldn't have thought about otherwise."

The Penn collaborators are working to plot the tracks of other cell types and credit their unique partnership for their discovery.

"We've said all along that this study could only happen because [our physics colleagues] had such a great expertise and we had our own separate expertise," Tajie Harris said. "They took a chance working with us, and it turned out to be something really rewarding."

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'Intelligent medicine' erases side effects

Scientists at Aarhus University, Denmark in collaboration with the biotech company Cytoguide now publish a key to use glucocorticoid steroids in a kind of intelligent medicine that specifically hits the relevant cells. Data are based on rodent studies but if this principle is translated to humans it may greatly improve todays hazardous treatment with this type of potent steroids.

This is the main perspective in the research now published in the recognized research journal Molecular Therapy in the Nature Publishing group.

50-fold higher potency

Synthetic glucocorticoid steroid are used in many acute and chronic inflammatory diseases including many autoimmune diseases such as rheumatoid arthritis. This is the most potent anti-inflammatory medicine, but its use is hampered by serious side effects such as osteoporosis, loss in muscle mass, diabetes and immunosuppression.

The new data from the scientists now show that they can target the drugs directly to the 'macrophage' immune cells. These cells play a main role in inflammation and their damaging effect on the surrounding tissues is strongly dampened by the glucocorticoid steroids.

The new technology is based on the coupling of the steroids to an antibody that specifically binds to a receptor exclusively expressed on the surface of macrophages. The receptors normally take up haemoglobin but they are also able to engulf drug-conjugates binding to the receptors. In the cells, the active steroid is released and it can now execute it effect (gene regulation).

In this way the drug only works in the relevant cells and much less is needed to obtain full efficacy.

Perspectives in many diseases

'Our project may initially have relevance for inflammation disease and our focus is now on the liver inflammation that affects many persons with fatty liver due to obesity or alcohol abuses' Soren K. Moestrup from Aarhus University says.

'But this technology may also be applied on completely different types of diseases such as cancer' he continues.

If the scientists get financing and collaboration with the large pharma industry in place they expect to have the first conjugate medicine on the market in about 6 years.

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Options for a NON GATE, B.Tech students to apply for M.Tech Biotechnology and allied programs

A non gate student has several options to apply for various M.Tech programs in Biotechnology and allied fields. So please don’t lose hope and apply to the options available right away. Below I have tried to give you the possible ways of admission into M.Tech and M. S. (by Research) courses in various IITs, NITs, some very good Universities and State Colleges along with certain Private Universities. Hope this mail proves to be helpful.

Indian Institute of Technology (IITs) or National Institute of Technology (NITs):

Sponsored Candidates:  If you are working in industry for over three year and can prove that your employer is ready to allow you to go to study by letters from authority, you can apply under this category. There are few seats reserved under this category in both IITs and NITs.

Quality Improvement Program (QIP): This is started by Govt. of India to improve the quality of teaching staff in state colleges by giving them a chance to attend India’s top most engineering schools. All the faculty members with three years plus experience are eligible for this.

M.Tech (Research): The National Institute of Technology, Rourkela, provides facilities for instructions in all Engineering Departments at postgraduate level with more emphasis on research content, leading to the degree of Master of Technology by Research, M. Tech. (Res). The M. Tech (Res) programmes are being offered by all of the Departments/ Centres National Institute Technology. For more details visit:

http://www.nitrkl.ac.in/Advertisement_for_Ph.D._admission_.pdf

In National Institute of Technology, Jalandar this programme is applicable to external faculty/staff working in organisations other than NITJ. Academic qualifications is Bachelor's degree in Engineering/Technology or Master's degree in appropriate Sciences/Humanities/Social Sciences with a first class or minimum 60% marks (CGPA 6.5) or equivalent. A valid GATE score of UGC/CSIR fellowship is not required. Candidates having a minimum of two years of professional experience after the qualifying degree in the appropriate discipline of the recognized institutes, R & D establishments, public utility undertakings and industrial units with well-established R & D units recognized by DST or NITJ are eligible. 

Other option: In NIT Durgapur, in case of non-availability of enough number of GATE-qualified candidates, the resulting vacant seats are filled with non-GATE candidates strictly based on merit through a written test followed by viva-voce. 30% weightage is given to written Test, 40% weightage to viva-voce in respective departments at NIT, Durgapur and 30% weightage to Percentage of Marks / CGPA obtained in the last qualifying examination. 

IIITs: These institutes are deemed universities and conduct their own entrance test for M.Tech course admission. For more details visit one of the Institute website:http://www.iiit.net/admissions/postgraduate/standingpg

Central Universities:Few Central Universities conduct their own entrance exam and few consider GATE scores too. Most of the State University doesn’t get GATE qualified students, therefore they conduct their own written test and interview. Examples of certain such universities and courses available are:

Hyderabad University: Medical Biotechnology, Bioinformatics

Jamia Millia Islamia: Nanotechnology, Environmental Engineering

Pondicherry University: Nano Science and Technology

On behalf of Anna University, Chennai, Cochin University of Science and Technology, Kochi, Kerala; &West Bengal University of Technology, Kolkata, Jawaharlal Nehru University holds Combined Biotechnology Entrance Examination for admission to M.Tech Biotechnology.

Deemed Universities: In recent years many good deemed universities have come with great infrastructure and industry interface.

State Universities: Few good universities in different states conduct their own test and follow admission procedure.

Private Universities: There are many private collages for Master Degree in Engineering (M.Tech) studies in every state.

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Walking and Running Again After Spinal Cord Injury

Rats with spinal cord injuries and severe paralysis are now walking (and running) thanks to researchers at EPFL. Published in the June 1, 2012 issue of Science, the results show that a severed section of the spinal cord can make a comeback when its own innate intelligence and regenerative capacity is awakened. The study, begun five years ago at the University of Zurich, points to a profound change in our understanding of the central nervous system. According to lead author Grégoire Courtine, it is yet unclear if similar rehabilitation techniques could work for humans, but the observed nerve growth hints at new methods for treating paralysis.

"After a couple of weeks of neurorehabilitation with a combination of a robotic harness and electrical-chemical stimulation, our rats are not only voluntarily initiating a walking gait, but they are soon sprinting, climbing up stairs and avoiding obstacles when stimulated," explains Courtine, who holds the International Paraplegic Foundation (IRP) Chair in Spinal Cord Repair at EPFL.

Waking up the spinal cord

It is well known that the brain and spinal cord can adapt and recover from moderate injury, a quality known as neuroplasticity. But until now the spinal cord expressed so little plasticity after severe injury that recovery was impossible. Courtine's research proves that, under certain conditions, plasticity and recovery can take place in these severe cases -- but only if the dormant spinal column is first woken up.

To do this, Courtine and his team injected a chemical solution of monoamine agonists into the rats. These chemicals trigger cell responses by binding to specific dopamine, adrenaline, and serotonin receptors located on the spinal neurons. This cocktail replaces neurotransmitters released by brainstem pathways in healthy subjects and acts to excite neurons and ready them to coordinate lower body movement when the time is right.

Five to 10 minutes after the injection, the scientists electrically stimulated the spinal cord with electrodes implanted in the outermost layer of the spinal canal, called the epidural space. "This localized epidural stimulation sends continuous electrical signals through nerve fibers to the chemically excited neurons that control leg movement. All that is left was to initiate that movement," explains Rubia van den Brand, contributing author to the study.

The innate intelligence of the spinal column

In 2009, Courtine already reported on restoring movement, albeit involuntary. He discovered that a stimulated rat spinal column -- physically isolated from the brain from the lesion down -- developed in a surprising way: It started taking over the task of modulating leg movement, allowing previously paralyzed animals to walk over treadmills. These experiments revealed that the movement of the treadmill created sensory feedback that initiated walking -- the innate intelligence of the spinal column took over, and walking essentially occurred without any input from the rat's actual brain. This surprised the researchers and led them to believe that only a very weak signal from the brain was needed for the animals to initiate movement of their own volition.

To test this theory, Courtine replaced the treadmill with a device that vertically supported the subjects, a mechanical harness did not facilitate forward movement and only came into play when they lost balance, giving them the impression of having a healthy and working spinal column. This encouraged the rats to will themselves toward a chocolate reward on the other end of the platform. "What they deemed willpower-based training translated into a fourfold increase in nerve fibers throughout the brain and spine -- a regrowth that proves the tremendous potential for neuroplasticity even after severe central nervous system injury," says Janine Heutschi, co-author in the study.

First human rehabilitation on the horizon

Courtine calls this regrowth "new ontogeny," a sort of duplication of an infant's growth phase. The researchers found that the newly formed fibers bypassed the original spinal lesion and allowed signals from the brain to reach the electrochemically-awakened spine. And the signal was sufficiently strong to initiate movement over ground -- without the treadmill -- meaning the rats began to walk voluntarily towards the reward, entirely supporting their own weight with their hind legs.

"This is the world-cup of neurorehabilitation," exclaims Courtine. "Our rats have become athletes when just weeks before they were completely paralyzed. I am talking about 100% recuperation of voluntary movement."

In principle, the radical reaction of the rat spinal cord to treatment offers reason to believe that people with spinal cord injury will soon have some options on the horizon. Courtine is optimistic that human, phase-two trials will begin in a year or two at Balgrist University Hospital Spinal Cord Injury Centre in Zurich, Switzerland. Meanwhile, researchers at EPFL are coordinating a nine million Euro project called NeuWalk that aims at designing a fully operative spinal neuroprosthetic system, much like the one used here with rats, for implanting into humans.

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Combined Biotech Entrance Exam

MORE THAN 10,000 aspirants appeared for the Combined Biotechnology Entrance Examination conducted on Thursday, 25th May for admission to 500 seats in 40 institutions.

If the numbers prove a point, it is that Biotechnology has arrived as a career choice for more young people than in the past. It is because biotechnology is increasingly being viewed as the magic bullet that can rid the world of many of its problems, from chronic hunger to infectious diseases. The belief, based more on fact than on hyperbole, has spawned industries, which in turn have created a rush of new job opportunities.

A little something about this exam:

Exam Pattern

The entrance examination, which is conducted by Jawaharlal Nehru University (JNU), is divided into two sections, and according to Prof. K. J. Mukherjee, Dean, School of Biotechnology, JNU. 

Section A has traditionally been beneficial for students who have studied Mathematics at the plus-two level, whereas students who had Biology in their undergraduate years have a clear edge in Section B. “Section A has Class XII-level questions from Physics, Chemistry, Biology, and Mathematics, so those who had Mathematics in their plus-two should get good scores in Section A,” Mukherjee said. 

“Section B has Physics and Chemistry, but there are more questions from Biology, which gives students who have studied biology an advantage.” Prof. Rajiv Bhat, Coordinator, Combined Biotechnology Entrance Examination, counsels test takers not to panic. “People who take the exam come from diverse academic backgrounds and it’s difficult to design a paper that includes all subjects,” Bhat said. “The paper is balanced and has questions from the subjects that matter to biotechnology students — Physics, Chemistry, Biology and Mathematics.” 

The really good news, though, is that students taking the examination won’t be as much in the dark about it as they have been all these years. To help aspirants prepare better, sample papers will be uploaded on the JNU website from next year, Bhat said.

JNU's School of Bio-Technology

It was one of the first six institutions in the country to initiate a postgraduate teaching and research programme in the subject in 1985. Over the years, it has established itself as the country’s leading academic programme in Biotechnology, which is why it has been given the responsibility of conducting and assessing the entrance examination.

The Common Entrance Examination is conducted for admission to the M. Sc. Biotechnology, M. Sc. Agriculture / M. V. Sc. ( Biotechnology) and M. Tech. Biotechnology programmes being offered by the participating institutions. 

JNU’s School of Biotechnology offers 30 M. Sc. seats, and the specialisations on offer include cell biology, biochemistry, biophysics, computational biology and bioinformatics, and biomolecules, to name just a few.

“We focus more on animal biotechnology and I think we are behind in plant biotechnology, though the School of Life Science does focus on this field,” Mukherjee added. The School, however, is introducing a paper in chemical and synthetic biology this academic session.

Among students, though, biotechnology industry courses such as biosimilars, advanced immunology and bioprocess technology are immensely popular, for they offer a diverse range of opportunities both in research and manufacturing. “ The production of cost- efficient drugs and food production is what biotechnology is being used for, so there are a number of career options in the industry,” Mukherjee added.

For more details :www.jnu.ac.in/Admission/BiotechAnnouncement2012-13.pdf

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New Molecular Structure Offers First Picture of a Protein Family Vital to Human Health

The 20 proteins in the Wnt family are some of the most important proteins in controlling how an organism develops and grows, but for 30 years scientists have not known what these vital proteins actually look like. The proteins have eluded standard visualization techniques, in large part because they do not dissolve well in the water-based liquids normally used for biochemical studies. But once Howard Hughes Medical Institute investigator K. Christopher Garcia, and Claudia Janda, a post-doctoral fellow in his Stanford University School of Medicine lab, thought of an approach to make the proteins behave better, they succeeded in solving the first structure of a Wnt protein.

Their work reveals an unexpected three-dimensional shape that offers clues to how Wnt proteins function and clarifies the nature of its Frizzled receptor target for drug developers working to design anti-Wnt therapies for cancer and other diseases. "Having finally gained structural access to Wnts, I think this is going to open up a whole new era in molecularly dissecting the role of Wnt proteins in biological processes," says Garcia.

Wnt proteins were discovered 30 years ago by Harold Varmus, the current director of the National Cancer Institute, and Roel Nusse, who is now an HHMI investigator at Stanford University. They observed that Wnt1, the gene for a Wnt protein, was very active in breast cancer cells from mice. Over the past decades, researchers have shown that Wnt proteins play key roles in embryonic development, tissue regeneration, bone growth, stem cell differentiation, as well as many human cancers. In essence, Wnt proteins help give cells their identity and tell them how to behave.

"This is one of the most important ligand-receptor systems in both human and invertebrate biology. Wnts cut across every field, which is why I got involved. But many excellent groups have tried to express them in the lab and solve their structures, so we realized that something non-intuitive would be required to crack the problem," says Garcia.

In 2003, Nusse's team found out why scientists who had been trying to isolate Wnt proteins had been plagued with so many difficulties: the proteins contained lipids, fatty molecules that prevent the protein from dissolving in water-based solutions. Scientists realized they could stabilize the protein by instead keeping it in mixtures that contained detergents, helping pave the way for a plethora of biochemical experiments on isolated Wnts. But such detergent-containing mixtures still present obstacles for crystallizing and visualizing proteins by structural analysis techniques; simply put, the detergents get in the way.

"This really causes a great deal of difficulty in working with these proteins," says Garcia. But he and Janda had an idea: what if they expressed both a Wnt protein, and the receptor it bound to in the same cell? Perhaps, they thought, the receptor would shield the Wnt protein's exposed lipid, making it able to dissolve in the solution they needed.

The technique worked -- they were able to produce Wnt8 bound to Frizzled-8, one of 10 Frizzled receptors that the 20 Wnt proteins bind to to carry out cellular effects.

"It's one of the most unusual protein structures I've ever seen," says Garcia. "It looks like a crab with its two pinchers reaching around and grabbing the Frizzled receptor. When we originally solved this, we could see no relationship between the structure of Wnt8 and any other structure that has ever been described. However, we are beginning to see the evolutionary origins of the Wnt fold. This story is developing."

Garcia expects the other Wnt proteins likely have similar structures, with the respective Frizzled receptors shielding the lipid attached to the protein, meaning their method should work on other Wnts. He now wants to delve into those structures, answering questions about which Wnt-Frizzled pairs are responsible for what biological roles, how co-receptors bind to the pairs, and how the structure can be changed to optimize the interactions.

"What we can see now are some clues in the structure as to why Wnts are so hard to express, because of the exposure of the lipid," says Garcia. "So now we can think about ways to remodel the protein that will solve the expression problem without altering function."

But it's not just basic science of Wnts that gets a boost with the new method for solving their structure, and the new structural data. Wnts have long been considered a potential drug target for cancers, as well as other diseases. Knowing the structure provides a huge advantage when trying to develop compounds that will bind to Wnts.

"There are already some drugs companies that have been developing anti-Wnt and anti-Frizzled antagonist antibodies as drugs," says Garcia. "But they're been working in the dark, with no knowledge of structure. So I really think this will open up a whole new era for not only of basic biology on these proteins, but also for their therapeutic potential. We are currently attempting to engineer Frizzled-specific Wnts in order to better understand the role of a particular Wnt in a biological and disease process, as well as assess the efficacy of selectively blocking or activating Wnt signaling pathways."

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Chief Minister chairs 2nd North East Biotech Hub Coordinators’ Interactive Meeting

Shri Pawan Chamling proposes setting up of Biotech Park in Sikkim

Gangtok, April 14, 2012: Two days long 2nd North East Biotech Hub Coordinators’ Interactive Meeting began today here at Chintan Bhawan, organised by Sikkim State Council of Science and Technology Gangtok, Department of Science and Technology and Climate Change, Government of Sikkim. The meeting supported by the Department of Biotechnology, Government of India, New Delhi, saw the presence of Chief Minister, Mr Pawan Chamling as chief guest along with Mr Bhim Dhungel, Minister for Science and Technology, Dr T. Madhan Mohan, Adviser, Department of Biotechnology, Government of India, New Delhi, Dr B. Ravindran, Director ILS, Bhubaneswar, Dr Purnima Sharma, MD & NERBPMC, New Delhi on the dais in the inaugural session. 

More than 100 Scientists and Research Scholars from Government of India and Institutional Hub Coordinators are participating in the meeting where they will be discussing on protection, conservation, monitoring and evaluation work on biodiversity and to foster exchange of ideas to promote Biotechnology in the North East region.

In his inaugural address, the Chief Minister informed that Sikkim- home to towering Mount Kanchenjunga and exquisite tapestry of flora and fauna, perhaps an exemplary State to ban killing of wildlife, felling of trees and use of plastics, where environmental conservation is paramount in all development philosophy. A State very close to attaining zero poverty status, wanting vigorously to pursue the ultimate aim of making Sikkim a total organic state. Sikkim accounts only 0.2% of total geographical area of the country, yet hosts over 26% of country’s biodiversity, he mentioned.

Respecting the sanctity of all living organisms including the green and clean environment, the Chief Minister further added that the State Government has undertaken many conservation measures to protect the mountain ecology and has moved very cautiously while undertaking any developmental activity. For Sikkim, conservation, protection of eco-system and environmental sanctity has remained priority, he added. The Chief Minister also infomed about the various innovative green initiatives taken by his government way back in 1995 like Harit Kranti Varsha, and the decade 2000 to 2010 as Harit Kranti Dasak, to generate mass awareness among the people through plantations. Other programmes like State Green Mission and Ten Minutes to earth have generated awareness about the conservation of environment and induced a sense of participation and ownership amongst the people.

Informing further, he said that registers are being maintained in each Gram Panchayat unit to record names of medicinal plants found in that area and for in-situ conservation on a regular basis and in the same manner he also asked the Department of Biotechnology, Government of India for supporting such endeavor in this field in a more extensive and comprehensive manner. This Coordinators’ Meeting is a common platform to discuss the issues and problems faced by the Biotech hub centers of the North Eastern states and it shall, no doubt, help the North Eastern states to work in close coordination with world experts on biotechnology both in India and outside the country, he mentioned. 


Mr Bhim Dhungel, in his address, mentioned that Science has made a noteworthy contribution to the global world in various sectors of medicine, agriculture, environment management and processing industry. Sikkim, blessed with natural beauty and rich biodiversity, is a treasure house of bioresources and protection and conservation of the same has been a priority in the state. He also believed that this two days meeting and the proceeding being published incorporating activities of all the Biotech- Hub Centres will serve as a valuable reference for the research organisations in the country. He also added that the exchange of intellectual ideas and thoughts during the meeting will lead to various recommendations and new ideas for strengthening of research in the field of biotechnology in the North Eastern region.

Dr T. Madhan Mohan, Adviser, Department of Biotechnology, Government of India, New Delhi expressed that biotechnology is a fast growing science that amalgamates biology and technology to derive a result using technological applications and has been used in many forms of traditional practices by the Indian society. The scheme on establishment of Biotech Hubs under the special programme for North East has been supported by the Department of Biotechnology, Government of India with the purpose of flourishing biotechnology in this region. The Adviser also advised the state government for capacity building for the students and hoped that north east can be a leading in biotechnology in the next five years. 

In her address, Dr Purnima Sharma, MD & NERBPMC, New Delhi said that the two days programme aims at interacting, sharing, learning from each other experiences and enhancing capacities in bio technology. 
Dr. B. Ravindran, Director, ILS (Institute of Life Sciences), Bhuwaneswar also shared his experiences.

The inaugural session also witnessed the release of books on Biodiversity of Sikkim and the proceeding of 2nd North East Biotech Hub Copordinators’ Meeting by the Chief Minister.

The technical session included the presentations by North East Coordinators, Institutional Hub Coordinators followed by the discussion with the Coordinators of Biotech Hubs. The second day shall also have the presentations by Institutional Hub Coordinators followed by the valedictory functions.

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