William G. Gilroy | December 17, 2014
A new study by Robert Stahelin, an adjunct associate professor of chemistry and biochemistry at the University of Notre Dame and an associate professor at the Indiana University School of Medicine-South Bend, as well as a member of Notre Dame’s Eck Institute for Global Health, investigates how the most abundant protein that composes the Ebola virus, VP40, mediates replication of a new viral particle.
“In brief, the Ebola virus has just seven proteins that encode in its genome,” Stahelin said. “VP40 is critical to the formation of a new viral particle and it does this by interacting with lipids inside human cells.”
Stahelin and co-investigator Smita Soni, a postdoctoral researcher at the Indiana University School of Medicine, found that VP40 is able to assemble in vitro (i.e., in a test tube), without any human cells present, and mediate formation of virus-like particles when the human lipid phosphatidylserine is found in solution with VP40, but not other control lipids.
“This means, in conjunction with our previous research papers, that Ebola virus VP40 can assemble and interact with human phosphatidylserine to generate the lipid coat of the virus,” Stahelin said. “For completeness’ sake, Ebola virus is a lipid-enveloped virus and gets its lipid bilayer coat from the human cell it infects. In essence, Ebola VP40 is assembling on phosphatidylserine-enriched regions of human cells to form the long filamentous virus particle we are so familiar with seeing.”
Read more at Harper Cancer Research Institute.