Email Print Share

News Release 08-220

Viruses, Start Your Engines!

Researchers find what drives one of nature's powerful, nanoscale motors

DNA entering the gp17 motor complex on the T4 capsid.

Image of DNA entering the gp17 motor complex on the T4 capsid.


December 29, 2008

For b-roll and sound bites including a sophisticated animation, an interview with researcher Michael Rossmann and b-roll of the laboratory, contact Dena Headlee at dheadlee@nsf.gov or Josh Chamot at jchamot@nsf.gov. Video is also available at: thenewsmarket.com.

This material is available primarily for archival purposes. Telephone numbers or other contact information may be out of date; please see current contact information at media contacts.

Peering at structures only atoms across, researchers have identified the clockwork that drives a powerful virus nanomotor.

Because of the motor's strength--to scale, twice that of an automobile--the new findings could inspire engineers designing sophisticated nanomachines. In addition, because a number of virus types may possess a similar motor, including the virus that causes herpes, the results may also assist pharmaceutical companies developing methods to sabotage virus machinery.

Researchers from Purdue University in West Lafayette, Ind., and the Catholic University of America in Washington, D.C., collaborated on the study that appears in the Dec. 26, 2008, issue of the journal Cell.

"The discovery of how this virus motor functions represents a significant milestone in the investigation of viral processes," says David Rockcliffe, the program director who oversees a National Science Foundation (NSF) grant that partly funded the research. "This research is a breakthrough that not only may lead to the development of a means of arresting harmful infections, but it also points to possible ways in which nano-devices could be fashioned,"

The virus in the study, called T4, is not a common scourge of people, but its host is: the bacterium Escherichia coli (E. coli). Purdue researchers studied the virus structures, such as the motor, while the Catholic University researchers isolated the virus components and performed biochemical analyses.

"T4 is what's called a 'tailed virus'," says Purdue biologist Michael Rossmann, one of the lead researchers for the study. "It is actually one of the most common types of organisms in the oceans of the world. There are many different, tailed, bacteria viruses--or phages--and all of these phages have such a motor for packaging their DNA, their genome, into their pre-formed heads."

The virus is well known to scientists. "T4 has rich history going back to 1940s when the original genetic tools to understand virus assembly were developed," adds biologist Venigalla Rao of Catholic University, also a lead researcher on the study. "T4 has been an important model system to tease out the details of basic mechanisms by which viruses assemble into infectious particles."

For the recent study, analyses involved two sophisticated instruments capable of studying structures at the nanometer (billionth of a meter) scale. One of the techniques, x-ray crystallography, showed the ordered arrays of atoms in the various structures, while another, called cryo-electron microscopy, let the researchers study the broader shape of the structures without the need for coating or drying out the specimens.

Having already determined the structures of a number of other viral components and how they self-assemble, in this study the researchers focused their attention on the small motor that some viruses use to package DNA into their "heads", protein shells also called capsids.

Not all viruses have a motor such as the one found  in the T4 virus, but some viruses that cause human diseases posses molecular motors with similar functions, and likely have similar structures. T4 uses its motor to pack about 171,000 basepairs of genetic information to near-crystalline density within its 120 nanometer by 86 nanometer capsid.

The researchers found that the motor is located at the intersection of the capsid and the virus "tail" and is made of a circular array of proteins called gene product 17 (gp17). Five, two-part, gp17 proteins combine to form a pair of conjoined rings, arrayed so that their upper segments form an upper ring and their lower segments form a lower ring.

As a T4 virus assembles itself, the lower ring of the motor structure attaches to a strand of DNA, while the upper ring attaches to a capsid. The upper and lower rings have opposite charges, which allow the motor to contract and release, alternately tugging at the DNA like a ring of hands pulling on a rope.

The process draws the DNA strand upwards into the capsid where it is protected from damage, enabling the virus to survive and reproduce. After the DNA is inside the capsid, the motor falls off, and a virus tail attaches to the capsid.

Until now, researchers did not know how T4, or any other virus, accomplished the DNA packaging. According to Rao, "Since the assembly of herpes viruses closely resembles that of T4, this research might provide insights on how to manipulate herpes infections."

While many questions remain, adds Rossmann, the virus may lend itself to a variety for medical purposes. One example Rossmann cites is as a potential new weapon to fight dangerous microbes.

"Bacteriophages like T4 are a completely alternative way of dealing with unwanted bacteria. The virus can kill bacteria in its process of reproduction, so use of such viruses as antibiotics has been a long looked-for alternative to overcome the problems which we now have with antibiotics."

For additional information, see the Purdue University press release at: http://news.uns.purdue.edu/x/2008b/081224RossmannMotors.html and the Catholic University press release at: http://publicaffairs.cua.edu/Releases/2008/09CUACellRelease.cfm

In collaboration with the researchers, animators at Seyet in West Lafayette, Ind., developed a sophisticated movie showing how a virus self-assembles and how the nanomotor works. The animation, along with other T4 animations developed through this collaboration, are available at: http://www.seyet.com/t4_academic.html

Prior research from Rossmann's lab was reported in the press release "Viruses on the Attack" at: http://www.nsf.gov/news/news_summ.jsp?cntn_id=100420

-NSF-

Media Contacts
 Joshua A. Chamot, NSF, (703) 292-7730, email: jchamot@nsf.gov
Emil Venere, Purdue University, (765) 494-4709, email: venere@purdue.edu
Victor Nakas, The Catholic University of America, (202) 319-5600, email: nakas@cua.edu

Program Contacts
 David Alexander Rockcliffe, NSF, (703) 292-7123, email: drockcli@nsf.gov

Principal Investigators
 Michael Rossmann, Purdue University, (765) 494 - 4911, email: mr@purdue.edu

Co-Investigators
 Venigalla Rao, The Catholic University of America, (202) 319-5271, email: rao@cua.edu

The U.S. National Science Foundation propels the nation forward by advancing fundamental research in all fields of science and engineering. NSF supports research and people by providing facilities, instruments and funding to support their ingenuity and sustain the U.S. as a global leader in research and innovation. With a fiscal year 2023 budget of $9.5 billion, NSF funds reach all 50 states through grants to nearly 2,000 colleges, universities and institutions. Each year, NSF receives more than 40,000 competitive proposals and makes about 11,000 new awards. Those awards include support for cooperative research with industry, Arctic and Antarctic research and operations, and U.S. participation in international scientific efforts.

mail icon Get News Updates by Email 

Connect with us online
NSF website: nsf.gov
NSF News: nsf.gov/news
For News Media: nsf.gov/news/newsroom
Statistics: nsf.gov/statistics/
Awards database: nsf.gov/awardsearch/

Follow us on social
Twitter: twitter.com/NSF
Facebook: facebook.com/US.NSF
Instagram: instagram.com/nsfgov