Host cyclophilin A mediates HIV-1 attachment to target cells via heparans

被引:143
作者
Saphire, ACS [1 ]
Bobardt, MD [1 ]
Gallay, PA [1 ]
机构
[1] Scripps Res Inst, Dept Immunol IMM9, La Jolla, CA 92037 USA
关键词
attachment; cyclophilin A; heparan; human immunodeficiency virus type-1;
D O I
10.1093/emboj/18.23.6771
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The present study proposes a novel mode of action for cyclophilin A (CypA) in the HIV-1 life cycle. We demonstrate that CypA-deficient viruses do not replicate Because they fail to attach to target cells. We show that CypA is exposed at the viral membrane and mediates HIV-1 attachment. We identify heparan as the exclusive cellular binding partner for CypA. Furthermore, CypA binds directly to heparan via a domain rich in basic residues similar to known heparin-binding motifs, This interaction between exposed CypA and cell surface heparans represents the initial step of HIV-1 attachment and is a necessary precursor to gp120-binding to CD4. In conclusion, HIV-1 attachment to target cells is a multi-step process that requires an initial CypA-heparan interaction followed by the gp120-CD4 interaction.
引用
收藏
页码:6771 / 6785
页数:15
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