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Journal of Virology, December 2005, p. 15586-15589, Vol. 79, No. 24
0022-538X/05/$08.00+0 doi:10.1128/JVI.79.24.15586-15589.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Trinity Zang, and
Paul D. Bieniasz*
Aaron Diamond AIDS Research Center and the Rockefeller University, New York, New York
Received 1 August 2005/ Accepted 20 September 2005
Defective human immunodeficiency virus type 1 (HIV-1) assembly in murine cells is accompanied by poor plasma membrane binding and proteolytic processing of the HIV-1 Gag precursor. Here, we show that such defects are induced by the propensity of the HIV-1 MA globular head to inhibit membrane binding and particle assembly, particularly at the low expression levels observed in murine cells. Simple additions to or deletion of the MA globular head can improve the yield of infectious virions from murine cells by >50-fold. Expression level and autoinhibition can be important confounding variables in studies of HIV-1 assembly and contribute to defects encountered in murine cells.
Present address: Department of Infectious Diseases GKT School of Medicine, King's College London, 2nd Floor, New Guy's House, Guy's Hospital, London SE1 9RT, United Kingdom.
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