HIV virions sense plasma membrane heterogeneity for cell entry
Author(s) -
SungTae Yang,
Alex J.B. Kreutzberger,
Volker Kiessling,
Barbie K. GanserPornillos,
Judith M. White,
Lukas K. Tamm
Publication year - 2017
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1700338
Subject(s) - membrane , receptor , human immunodeficiency virus (hiv) , plasma , microbiology and biotechnology , domain (mathematical analysis) , cell , cell membrane , fuse (electrical) , sense (electronics) , virology , biophysics , chemistry , biology , biochemistry , physics , mathematical analysis , mathematics , quantum mechanics
It has been proposed that cholesterol in host cell membranes plays a pivotal role for cell entry of HIV. However, it remains largely unknown why virions prefer cholesterol-rich heterogeneous membranes to uniformly fluid membranes for membrane fusion. Using giant plasma membrane vesicles containing cholesterol-rich ordered and cholesterol-poor fluid lipid domains, we demonstrate that the HIV receptor CD4 is substantially sequestered into ordered domains, whereas the co-receptor CCR5 localizes preferentially at ordered/disordered domain boundaries. We also show that HIV does not fuse from within ordered regions of the plasma membrane but rather at their boundaries. Ordered/disordered lipid domain coexistence is not required for HIV attachment but is a prerequisite for successful fusion. We propose that HIV virions sense and exploit membrane discontinuities to gain entry into cells. This study provides surprising answers to the long-standing question about the roles of cholesterol and ordered lipid domains in cell entry of HIV and perhaps other enveloped viruses.
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