The HIV-1 gp120 Major Variable Regions Modulate Cold Inactivation

被引:20
作者
Medjahed, Halima [1 ,2 ]
Pacheco, Beatriz [4 ,5 ]
Desormeaux, Anik [1 ]
Sodroski, Joseph [4 ,5 ,6 ,7 ]
Finzi, Andres [1 ,2 ,3 ]
机构
[1] Univ Montreal, Ctr Rech CHUM, Montreal, PQ, Canada
[2] Univ Montreal, Dept Microbiol & Immunol, Montreal, PQ H3C 3J7, Canada
[3] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[4] Harvard Univ, Sch Med, Dept Canc Immunol & AIDS, Dana Farber Canc Inst, Boston, MA USA
[5] Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Aids, Boston, MA USA
[6] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[7] Ragon Inst Massachusetts Gen Hosp, Massachusetts Inst Technol & Harvard, Charlestown, MA USA
基金
加拿大创新基金会; 美国国家卫生研究院;
关键词
ENVELOPE GLYCOPROTEIN; GP41; ANTIBODIES; COFACTOR; RECEPTOR;
D O I
10.1128/JVI.03124-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
HIV-1 entry involves the viral envelope glycoproteins (Env gps) and receptors on the target cell. Receptor binding channels the intrinsic high potential energy of Env into the force required to fuse the membranes of virus and target cell. For some HIV-1 strains, prolonged incubation on ice decreases Env potential energy and results in functional inactivation. By characterizing chimeras between two primary clade C HIV-1 strains that differ in sensitivities to cold, soluble CD4, and neutralizing antibodies, we found that these properties were largely determined by discrete elements within the gp120 variable regions V1V2 and V3.
引用
收藏
页码:4103 / 4111
页数:9
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