Short report

Importance of disulphide bonds for vaccinia virus L1R protein function

Robert E Blouch¹ , Chelsea M Byrd² and Dennis E Hruby^1,2

¹  Department of Microbiology, Oregon State University, 220 Nash Hall, Corvallis, Oregon, 97331, USA

²  Siga Technologies, 4575 SW Research Way, Suite 230, Corvallis, Oregon, 97333, USA

author email corresponding author email

Virology Journal 2005, 2:91doi:10.1186/1743-422X-2-91

Published:	9 December 2005

Abstract

L1R, a myristylated late gene product of vaccinia virus, is essential for formation of infectious intracellular mature virions (IMV). In its absence, only viral particles arrested at an immature stage are detected and no infectious progeny virus is produced. Previous studies have shown that the L1R protein is exclusively associated with the IMV membrane and that myristylation is required for correct targeting. The L1R protein contains six cysteine amino acid residues that have all been shown to participate in intramolecular disulphide bonds. However, it was not clear what role, if any, the disulfide bonds play in the membrane topology of the L1R protein. To address this question, a comprehensive library of L1R mutants in which the cysteine residues have been mutated to serine (either individually or in combination) were tested for their ability to rescue a L1R conditional lethal mutant virus under non-permissive conditions. Much to our surprise, we determined that C57 was not essential for production of infectious IMV. These results suggest that protein disulphide isomerases may be involved in reorganization of disulfide bonds within the L1R protein.