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Journal of Virology, February 2008, p. 2025-2027, Vol. 82, No. 4
0022-538X/08/$08.00+0 doi:10.1128/JVI.02278-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Manidipa Banerjee,2
Anette Schneemann,2 and
John E. Johnson1,2*
Department of Chemistry and Biochemistry, University of California—San Diego,1 Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 920372
Received 20 October 2007/ Accepted 29 November 2007
The infectivity of flock house virus (FHV) requires autocatalytic maturation cleavage of the capsid protein at residue 363, liberating the C-terminal 44-residue
peptides, which remain associated with the particle. In vitro studies previously demonstrated that the amphipathic, helical portion (amino acids 364 to 385) of
is membrane active, suggesting a role for
in RNA membrane translocation during infection. Here we show that the infectivity of a maturation-defective mutant of FHV can be restored by viruslike particles that lack the genome but undergo maturation cleavage. We propose that the colocalization of the two defective particle types in an entry compartment allows the restoration of infectivity by
.
Published ahead of print on 12 December 2007.
Present address: Department of Cell and Developmental Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801.
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