Saphire A C, Bobardt M D, Gallay P A
Department of Immunology IMM-9, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
EMBO J. 1999 Dec 1;18(23):6771-85. doi: 10.1093/emboj/18.23.6771.
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.
本研究提出了亲环素A(CypA)在HIV-1生命周期中的一种新作用模式。我们证明,缺乏CypA的病毒无法复制,因为它们无法附着于靶细胞。我们表明,CypA暴露于病毒膜上并介导HIV-1的附着。我们确定硫酸乙酰肝素是CypA唯一的细胞结合伴侣。此外,CypA通过一个富含碱性残基的结构域直接与硫酸乙酰肝素结合,该结构域类似于已知的肝素结合基序。暴露的CypA与细胞表面硫酸乙酰肝素之间的这种相互作用代表了HIV-1附着的初始步骤,并且是gp120与CD4结合的必要前提。总之,HIV-1与靶细胞的附着是一个多步骤过程,需要首先发生CypA-硫酸乙酰肝素相互作用,随后是gp120-CD4相互作用。