Purdue News
Purdue News
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August 18, 2003 Purdue researchers expose 'docking bay' for viral attackWEST LAFAYETTE, Ind. – Imagine a virus and its cellular target as two spacecraft – the virus sporting a tiny docking bay that allows it to invade its victim. Purdue University researchers have taken a close-up picture of one virus' docking bay, work that could have implications for both medicine and nanotechnology.
Using advanced imaging techniques, an international team of biologists led by Michael Rossmann of Purdue, Vadim Mesyanzhinov in Moscow and Fumio Arisaka at the Tokyo Institute of Technology has analyzed the structure of part of the T4 virus, which commonly infects E. coli bacteria. The part they analyzed, called the baseplate, is a complex structure made of 16 types of proteins that allows T4 to attach itself to the surface of E. coli in order to inject its own deadly genetic material. Their work has produced the clearest picture ever obtained of the baseplate, which plays a critical role in the initial stages of viral infection. "We now have a fairly complete picture of the baseplate, the part of the virus that latches onto its cellular victim," said Rossmann, who is Hanley Distinguished Professor of Biological Sciences in Purdue's School of Science. "Armed with this knowledge, we should obtain a better understanding of how this virus injects its genetic material into its host. It could be the key to stopping the process – or even harnessing it to benefit humanity." The paper appears in the latest issue (Sunday, 8/17) of Nature Structural Biology.
While T4 is perhaps not as well known as the viruses that cause the flu, it is an old friend of viral researchers as an invader of the E. coli bacterium, which itself can threaten human health. Viruses that attack bacteria, called bacteriophages, are readily studied because a virus that attacks a unicellular host can often be observed and manipulated more easily. "Mesyanzhinov, Arisaka and I discussed the possibility of examining T4 in closer detail," said Rossmann. "It's a very complicated structure consisting of more than 150 protein molecules, and we wanted to know how they were put together. So we decided to take a close look." It had been common scientific knowledge that the baseplate was a complicated but beautiful mechanism, one which changed its conformation from a hexagon to a star shape as it formed the irrevocable bond between virus and bacterium. Analysis of its protein building blocks required the use of both electron microscopy, needed to resolve the shapes and relationships between the proteins, and X-ray crystallography, needed for high-resolution images of the atoms within them. Each of the three researchers contributed some of the technology necessary for the analysis, which eventually revealed the structure of the baseplate. "There are several steps a virus takes to infect a host cell," Rossmann said. "Scientists have long known what the steps were, but no one had ever examined them on a molecular level before. This research should allow us to analyze the initial events in a viral attack. Such knowledge could be useful for targeting bacterial viruses to kill invading bacteria as an alternative to antibiotic compounds." While viruses are not generally thought of as prospective friends to mankind, many attack the very bacteria that cause common human illnesses, giving them potential as antibiotics. "T4 attacks E. coli, which is well known as a threat to human health," Rossmann said. "Many other bacteriophages also have structures similar to T4. If we could modify the proteins in the baseplate's attachment fibers, it might enable T4 to destroy harmful bacteria. This research could be a step in that direction." Nanotechnology applications also are possible. "The baseplate of this virus is essentially a complex molecular machine," Rossmann said. "We have now obtained a clear picture of its structure, which has allowed us to suggest how it works. Building nanomachines will likely be easier if we can borrow some mechanisms already proven by nature." Such applications are admittedly pie in the sky for the moment, and Rossmann said the most valuable result of the research is the fundamental knowledge it reveals about viruses. "We now have a close-up image of the machinery that guides the steps taken when a virus infects a cell," he said. "We hope further analyses will show even greater detail." This research was funded in part by grants from the National Science Foundation, the Howard Hughes Medical Institute and the Human Frontiers Science Program. Rossmann's team is associated with Purdue's Markey Center for Structural Biology, which consists of laboratories that use a combination of cryoelectron microscopy, crystallography and molecular biology to elucidate the processes of viral entry, replication and pathogenesis. Writer: Chad Boutin, (765) 494-2081, cboutin@purdue.edu Sources: Michael G. Rossmann, (765) 494-4911, mgr@indiana.bio.purdue.edu Petr G. Leiman, (765) 494-4925, leiman@purdue.edu Purdue News Service: (765) 494-2096; purduenews@purdue.edu
CAPTION: CAPTION: Three-dimensional structure of Victor A Kostyuchenko, Petr G Leiman, The baseplate of bacteriophage T4 is a multi-protein molecular machine that controls host cell recognition, attachment, tail sheath contraction and viral DNA ejection. The three-dimensional structure of the baseplate-tail tube complex has been determined to 12 Å resolution by cryoelectron microscopy. The baseplate has a six-fold symmetric, dome-like structure about 520 Å in diameter and 270 Å long, assembled around a central hub. A 940 Å-long and 96 Å-diameter tail tube, coaxial with the hub, is connected to the top of the baseplate. At the center of the dome is a needle-like structure that was previously identified as a cell-puncturing device. The locations of six proteins with known atomic structures have been identified. In addition, the position and shape of some other baseplate proteins also have been established. The baseplate structure suggests a mechanism of baseplate triggering and structural transition during the initial stages of T4 infection.
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