HIV gp120 interactions with coreceptors: Insights from studies with CCR5-based peptides

被引:0
|
作者
Berger, Edward A.
Alkhatib, Ghalib
机构
[1] NIAID, NIH, Viral Dis Lab, Bethesda, MD 20892 USA
[2] Indiana Univ, Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
关键词
HIV; AIDS; coreceptor; CCR5; CXCR4; chemokine receptor; CD4; GPCR; peptides; fusion; entry;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Human immunodeficiency virus enters cells by a direct fusion mechanism triggered by sequential binding of the gp120 subunit of the envelope glycoprotein, first to CD4, then to the coreceptor CCR5 or CXCR4. The coreceptors are chemokine receptors, members of the superfamily of G protein-coupled receptors that are characterized by 7 transmembrane domains. gp120 is presumed to interact with the extracellular portion, which consists of the N-terminal segment and three extracellular loops. Synthetic peptides based on these regions have proven to be valuable probes for elucidating the molecular details of the complex gp120-coreceptor interactions.
引用
收藏
页码:403 / 407
页数:5
相关论文
共 50 条
  • [1] The HIV-1 gp120 interaction with Nt-CCR5-New insights from NMR
    Schnur, E.
    Scherf, T.
    Naider, F.
    Anglister, J.
    [J]. FEBS JOURNAL, 2010, 277 : 240 - 241
  • [2] CCR5 interactions with the variable 3 loop of gp120
    Napier, Kelby B.
    Wang, Zi-xuan
    Peiper, Stephen C.
    Trent, John O.
    [J]. JOURNAL OF MOLECULAR MODELING, 2007, 13 (01) : 29 - 41
  • [3] Theoretical Studies on the Interactions and Interferences of HIV-1 Glycoprotein gp120 and Its Coreceptor CCR5
    Da, Lin-tai
    Wu, Yun-Dong
    [J]. JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2011, 51 (02) : 359 - 369
  • [4] CCR5 interactions with the variable 3 loop of gp120
    Kelby B. Napier
    Zi-xuan Wang
    Stephen C. Peiper
    John O. Trent
    [J]. Journal of Molecular Modeling, 2007, 13 : 29 - 41
  • [5] Modeling interaction between gp120 HIV protein and CCR5 receptor
    Guryanov, I.
    Real-Fernandez, F.
    Sabatino, G.
    Prisco, N.
    Korzhikov-Vlakh, V.
    Biondi, B.
    Papini, A. M.
    Korzhikova-Vlakh, E.
    Rovero, P.
    Tennikova, T.
    [J]. JOURNAL OF PEPTIDE SCIENCE, 2019, 25 (02)
  • [6] gp120 Envelope glycoproteins of human immunodeficiency viruses competitively antagonize signaling by coreceptors CXCR4 and CCR5
    Madani, N
    Kozak, SL
    Kavanaugh, MP
    Kabat, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (14) : 8005 - 8010
  • [7] Models of HIV-1 gp120 Complexed with CXCR4 and CCR5
    Agarwal, A.
    Stein, R. A.
    Cardozo, T.
    [J]. AIDS RESEARCH AND HUMAN RETROVIRUSES, 2013, 29 (11) : A82 - A83
  • [8] THE GP120 ENVELOPE OF HIV BINDS PEPTIDES IN A SIMILAR MANNER TO HLA
    DALGLEISH, AG
    SHEIKH, MJ
    ONGRADI, J
    AUSTEN, BM
    [J]. AIDS RESEARCH AND HUMAN RETROVIRUSES, 1995, 11 : S85 - S85
  • [9] A biochemical approach for detecting interactions between peptides from the HIV gp120 glycoprotein and a CD4 sequence
    Chersi, A
    Falasca, G
    Malorni, W
    [J]. ZEITSCHRIFT FUR NATURFORSCHUNG SECTION C-A JOURNAL OF BIOSCIENCES, 2004, 59 (9-10): : 734 - 738
  • [10] CCR5-based HIV entry inhibitors share five features
    不详
    [J]. CHEMICAL & ENGINEERING NEWS, 2003, 81 (40) : 24 - 24