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Journal of Virology, June 2003, p. 7067-7077, Vol. 77, No. 12
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.12.7067-7077.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Progressive Truncations C Terminal to the Membrane-Spanning Domain of Simian Immunodeficiency Virus Env Reduce Fusogenicity and Increase Concentration Dependence of Env for Fusion

Xiaoxu Lin,1,{dagger} Cynthia A. Derdeyn,1 Robert Blumenthal,2 John West,1 and Eric Hunter1*

Department of Microbiology, The University of Alabama at Birmingham, Birmingham, Alabama 35294,1 Section of Membrane Structure and Function, Laboratory of Experimental and Computational Biology, National Cancer Institute—Frederick Cancer Research and Development Center, Frederick, Maryland 217022

Received 21 November 2002/ Accepted 24 March 2003

The simian immunodeficiency virus (SIV) transmembrane (TM) protein, gp41, has multiple functions, which include anchoring the glycoprotein complex in the lipid envelope of the virus and mediating fusion of the virus and host cell membranes. Recently, a series of mutants of the SIVmac239 TM protein that have truncations at the carboxyl terminus of the membrane-spanning domain (MSD) have been characterized (J. T. West, P. Johnston, S. R. Dubay, and E. Hunter, J. Virol. 75:9601-9612, 2001). These mutants retained membrane anchorage but demonstrated reduced fusogenicity and infectivity as the MSD length was shortened. We have established a novel three-color fluorescence assay, which allows qualitative confocal and quantitative flow cytometric analyses, to further characterize the nature of the fusion defect in five of the MSD mutants: TM185, TM186, TM187, TM188, and TM189. Our analysis showed that each mutant could mediate complete lipid and aqueous dye transfer at early time points after effector and target cell mixing. No hemifusion with only lipid dye flux was detected. However, another intermediate fusion stage, which appears to involve small-fusion-pore formation that allowed small aqueous dye transfer but prevented the exchange of large cytoplasmic components, was identified infrequently in mutant-Env-expressing cell and target cell mixtures. Quantitative flow cytometric analysis of these mutants demonstrated that the TM187, TM188, and TM189 mutants were significantly more fusogenic than TM185 and TM186 but remained significantly impaired compared to the wild type. Moreover, fusion efficiency showed an increased dependence on the expression level of glycoproteins, suggesting that, for these mutants, formation of an active fusion complex was an increasingly stochastic event.

* Corresponding author. Mailing address: Department of Microbiology, The University of Alabama at Birmingham, 256 Bevill Biomedical Res. Bldg., 845 19th St. South, Birmingham, AL 35294-2170. Phone: (205) 934-4321. Fax: (205) 934-1640. E-mail: ehunter{at}uab.edu.

{dagger} Present address: Department of Microbiology and Immunology, Emory University, Atlanta, GA 30329.

Journal of Virology, June 2003, p. 7067-7077, Vol. 77, No. 12
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.12.7067-7077.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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