January 30, 2002
Study reveals new information on how viruses enter cells
WEST LAFAYETTE, Ind. A detailed look at a syringe-like structure designed to inject viral DNA into a host cell reveals a unique and complex entry scheme for viruses.
The study may provide clues to how similar viruses infect cells and suggest ways for developing a new class of antibiotics and other drugs to prevent illnesses caused by viral pathogens.
Scientists at Purdue University have solved the three-dimensional structure of the bacteriophage T4 virus, a virus that resembles a lunar lander in both its looks and intricate workings.
The study, published in the Jan. 31 issue of the journal Nature, reveals for the first time how the virus binds to the surface of the host, punctures the cell wall with a syringe-like tube and injects its own genetic blueprint into the cell. This genetic information then sets the cell's machinery to work creating replicas of the virus.
"Though the T4 virus has been studied extensively in the past, this study provides the first detailed information on the virus structure and how it works," says Michael Rossmann, Hanley Distinguished Professor of Biological Sciences at Purdue who directed the study.
Bacteriophage T4 is a virus that infects only bacteria, in this case E. coli, a bacteria used extensively in molecular biology research. The study of bacterial viruses such as T4 is useful in understanding many basic functions in biology, Rossmann says.
"This particular study tells us a great deal about how a virus infects a cell," he says. "These processes tend to be quite general, so mechanisms used by one virus often are similar to mechanisms used by other viruses, including those that infect humans."
Bacteriophages may play a future role in controlling disease-causing bacteria, says Kamal Shukla, the National Science Foundation project officer for this research.
"Knowing the exact mechanism of T4 bacteriophage infectivity is a significant breakthrough," Shukla says. "This information could eventually help in creating designer viruses that could be the next class of antibiotics."
Analysis of the cell-puncturing device also reveals a structure that may hold potential for applications in nanotechnology, such as microscopic probes, Rossmann says.
"This a very stable structure that looks like a small stylus," he says. "It might be useful as a probe in an atomic force microscope, which employs a probe of molecular dimension."
The T4 virus consists of an elongated head, which carries the virus' genetic material, and a tail made up of a hexagonal baseplate and six leg-type structures, called long-tail and short-tail fibers.
In the study, the Purdue group analyzed atom-by-atom the structure of the virus' baseplate. The baseplate is the key component of the virus, Rossmann says, serving as a "nerve center" and sending signals to and from the virus' head and tail fibers.
While transmitting its messages, the baseplate also prepares the virus machinery to eject its DNA into the host cell.
"A whole series of events are required to recognize, attach and confirm the attachment, and then contract so that the viral DNA can be ejected into the host," Rossmann says. "It's a very complicated system for infecting a cell."
The viral machine works as follows:
The virus uses its long-tail fibers to recognize its host and to send a signal back to the baseplate. Once the signal is received, the short-tail fibers help anchor the baseplate into the cell surface receptors. As the virus sinks down onto the surface, the baseplate undergoes a change shifting from a hexagon to a star-shaped structure. At this time, the whole tail structure shrinks and widens, bringing the internal pin-like tube in contact with the outer membrane of the E. coli cell. As the tail tube punctures the outer and inner membranes of the E. coli cell, the virus' DNA is injected through the tail tube into the host cell.
The DNA then instructs the bacterium to produce new viruses. So many are produced, in fact, that the E. coli eventually bursts, setting masses of new virus free to infect other cells.
The new detailed images provided by Rossmann's group also reveal a structure slightly different than what scientists had envisioned.
"We found that the baseplate is shaped like a cup or small dome," Rossmann says. "Previously it was believed that the baseplate was a rather flat structure."
The study also is the first to show how the syringe-like tube is situated in the center of the baseplate, positioned in line with the DNA contained in the virus head.
The studies were done at Purdue using X-ray crystallography, a technique often used to study structures such as proteins and viruses, in atomic detail. But the process works only if the substances can be made to form crystals. Crystals are used because the diffraction pattern from one single molecule could be insignificant, but the many individual, identical molecules in a crystal amplify the pattern.
Diffraction patterns are created when an X-ray beam hits a crystal, causing the electrons surrounding each atom to bend the beam. Computers can then be used to interpret this pattern and reconstruct the positions of the atoms.
"Because the structure is so complex, we could not crystallize the entire virus structure at once," Rossmann says. "Instead, we crystallized the various components and gradually pieced together a picture of the structure."
The research was funded by the National Science Foundation. Rossmann and his research team at Purdue collaborated with Shuji Kanamaru and Fumio Arisaka of the Tokyo Institute of Technology, and Vadim Mesyanzhinov of the Shemyakin-Ovchnnikov Institute of Bioorganic Chemistry in Moscow, Russia.
Writer: Susan Gaidos, (765) 494-2081; firstname.lastname@example.org
Sources: Michael Rossmann, (765) 494-4991, email@example.com
Kamal Shukla, (703) 292-8444, firstname.lastname@example.org
Purdue News Service: (765) 494-2096; email@example.com
A publication-quality photograph is available at ftp://ftp.purdue.edu/pub/uns/rossmann.T4.jpeg.
The Structure of the Bacteriophage T4 Cell-Puncturing Device
Shuji Kanamaru, Petr G. Leiman, Victor A. Kostyuchenko, Paul R. Chipman, Vadim V. Mesyanzhinov,
Bacteriophage T4 has a very efficient mechanism for infecting cells. The key component of this process is the baseplate, located at the end of the phage tail, which regulates the interaction of the tail fibers and the DNA ejection machine. The complex of gene product (gp) 5 (63°kDa) and gp27 (44°kDa), the central part of the baseplate, is required to penetrate the E. coli outer cell membrane and to disrupt the inter membrane peptidoglycan layer, promoting subsequent page DNA entry into the host. We present here a crystal structure of the (gp5-gp27)3 321°kDa complex determined to 2.9° resolution fitted into a 17° resolution cyro-electron microscopy image reconstruction of the baseplate-tail assembly.