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Conserved structures exposed in HIV-1 envelope glycoproteins stabilized by flexible linkers as potent entry inhibitors and potential immunogens

  1. Author:
    Chow, Y. H.
    Wei, O. L.
    Phogat, S.
    Sidorov, I. A.
    Fouts, T. R.
    Broder, C. C.
    Dimitrov, D. S.
  2. Author Address

    NCI, Lab Expt & Computat Biol, NIH, Bldg 469,Rm 246,POB B,Miller Dr, Frederick, MD 21702 USA NCI, Lab Expt & Computat Biol, NIH, Frederick, MD 21702 USA Uniformed Serv Univ Hlth Sci, Dept Microbiol & Immunol, Bethesda, MD 20814 USA Univ Maryland, Inst Biotechnol, Inst Human Virol, Baltimore, MD 21201 USA Dimitrov DS NCI, Lab Expt & Computat Biol, NIH, Bldg 469,Rm 246,POB B,Miller Dr, Frederick, MD 21702 USA
    1. Year: 2002
  1. Journal: Biochemistry
    1. 41
    2. 22
    3. Pages: 7176-7182
  2. Type of Article: Article
  1. Abstract:

    The HIV-1 envelope glycoprotein (Env) undergoes conformational changes while driving entry. We hypothesized that some of the intermediate Env conformations could be represented in tethered constructs where gp120 and the ectodomain of gp41 are joined by flexible linkers. Tethered Envs with long linkers (gp140-14 with 15 aa and gp140-24 with 26 aa) were stable and recognized by conformationally dependent anti-gp120 and anti-ap41 monoclonal antibodies (mAbs). Surprisingly, these proteins potently inhibited membrane fusion mediated by R5, X4, and R5X4 Envs with 5-100-fold lower IC50 than a tethered Env with short linker (gp140-4 with 4 aa), gp 120, gp 140, soluble CD4, or DP178 (T20). Compared to gp 140, gp140-14,24 exhibited increased binding to anti-gp41 cluster II mAbs but not to cluster I mAbs. Cluster II mAbs but not cluster I, IV, or V mAbs reversed the inhibitory effect of gp140-14,24 suggesting a rote of exposed conserved gp41 structures for the mechanism of inhibition. These findings suggest the existence of conserved gp41 structures that are important for HIV-1 entry and can be stably exposed in the native environment of the Env even in the absence of receptor-mediated activation. Thus, tethered Envs with long linkers may not only be important as HIV-1 inhibitors but also for elucidation of viral entry mechanisms and development of novel vaccine immunogens.

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