Inhibiting HIV-1 entry: Discovery of D-peptide inhibitors that target the gp41 coiled-coil pocket

被引:412
作者
Eckert, DM [1 ]
Malashkevich, VN [1 ]
Hong, LH [1 ]
Carr, PA [1 ]
Kim, PS [1 ]
机构
[1] MIT, Howard Hughes Med Inst, Whitehead Inst Biomed Res, Dept Biol,Cambridge Ctr 9, Cambridge, MA 02142 USA
关键词
D O I
10.1016/S0092-8674(00)80066-5
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 HIV-1 gp41 protein promotes viral entry by mediating the fusion of viral and cellular membranes. A prominent pocket on the surface of a central trimeric coiled coil within gp41 was previously identified as a potential target for drugs that inhibit HIV-1 entry. We designed a peptide, IQN17, which properly presents this pocket. Utilizing IQN17 and mirror-image phage display, we identified cyclic, D-peptide inhibitors of HIV-1 infection that share a sequence motif. A1.5 Angstrom cocrystal structure of IQN17 in complex with a D-peptide, and NMR studies, show that conserved residues of these inhibitors make intimate contact with the gp41 pocket. Our studies validate the pocket per se as a target for drug development. IQN17 and these D-peptide inhibitors ave likely to be useful for development and identification of a new class of orally bioavailable anti-HIV drugs.
引用
收藏
页码:103 / 115
页数:13
相关论文
共 50 条
  • [1] [Anonymous], ACTA CRYSTALLOGR D
  • [2] Chemokine receptors as HIV-1 coreceptors: Roles in viral entry, tropism, and disease
    Berger, EA
    Murphy, PM
    Farber, JM
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1999, 17 : 657 - 700
  • [3] TRIMERIC SUBDOMAIN OF THE SIMIAN IMMUNODEFICIENCY VIRUS GLYCOPROTEIN
    BLACKLOW, SC
    LU, M
    KIM, P
    [J]. BIOCHEMISTRY, 1995, 34 (46) : 14955 - 14962
  • [4] Bovey F. A., 1988, NUCL MAGNETIC RESONA
  • [5] Crystallography & NMR system:: A new software suite for macromolecular structure determination
    Brunger, AT
    Adams, PD
    Clore, GM
    DeLano, WL
    Gros, P
    Grosse-Kunstleve, RW
    Jiang, JS
    Kuszewski, J
    Nilges, M
    Pannu, NS
    Read, RJ
    Rice, LM
    Simonson, T
    Warren, GL
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1998, 54 : 905 - 921
  • [6] EFFECTS OF AMINO-ACID CHANGES IN THE EXTRACELLULAR DOMAIN OF THE HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 GP41 ENVELOPE GLYCOPROTEIN
    CAO, J
    BERGERON, L
    HELSETH, E
    THALI, M
    REPKE, H
    SODROSKI, J
    [J]. JOURNAL OF VIROLOGY, 1993, 67 (05) : 2747 - 2755
  • [7] CAVANAGH J, 1993, J MAGN RESON SER A, V105, P328
  • [8] Cavanagh J., 1996, PROTEIN NMR SPECTROS
  • [9] Core structure of gp41 from the HIV envelope glycoprotein
    Chan, DC
    Fass, D
    Berger, JM
    Kim, PS
    [J]. CELL, 1997, 89 (02) : 263 - 273
  • [10] Evidence that a prominent cavity in the coiled coil of HIV type 1 gp41 is an attractive drug target
    Chan, DC
    Chutkowski, CT
    Kim, PS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) : 15613 - 15617