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CD4-lndependent Binding of SIV gp120 to Rhesus CCR5

机译:SIV gp120与恒河猴CCR5的CD4依赖性结合

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CCR5 and CD4 are coreceptors for immunodeficiency virus entry into target cells. The gp120 envelope glycoprotein from human immunodeficiency virus strain HIV-1(YU2) bound human CCR5 (CCR5_(hu)) or rhesus macaque CCR5 (CCR5_(rh)) only in the presence of CD4. The gp120 from simian immunodeficiency virus strain SIVmac239 bound CCR5_(rh) without CD4, but CCR5_(hu) remained CD4-dependent. The CD4-independent binding of SIVmac239 gp120 depended on a single amino acid, Asp~(13), in the CCR5_(rh) amino-terminus. Thus, CCR5-binding moieties on the immunodeficiency virus envelope glycoprotein can be generated by interaction with CD4 or by direct interaction with the CCR5 amino-terminus. These results may have implications for the evolution of receptor use among lentiviruses as well as utility in the development of effective intervention.
机译:CCR5和CD4是免疫缺陷病毒进入靶细胞的共受体。仅在CD4存在的情况下,来自人免疫缺陷病毒株HIV-1(YU2)的gp120包膜糖蛋白结合人CCR5(CCR5_(hu))或恒河猴CCR5(CCR5_(rh))。来自猿免疫缺陷病毒株SIVmac239的gp120结合了没有CD4的CCR5_(rh),但是CCR5_(hu)仍然是CD4依赖性的。 SIVmac239 gp120的不依赖CD4的结合取决于CCR5_(rh)氨基末端的单个氨基酸Asp〜(13)。因此,免疫缺陷病毒包膜糖蛋白上的CCR5结合部分可通过与CD4相互作用或与CCR5氨基末端直接相互作用而产生。这些结果可能对慢病毒之间受体使用的演变以及有效干预措施的实用性产生影响。

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