AMD310, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor

被引:655
作者
Donzella, GA
Schols, D
Lin, SW
Esté, JA
Nagashima, KA
Maddon, PJ
Allaway, GP
Sakmar, TP
Henson, G
De Clercq, E
Moore, JP
机构
[1] Rockefeller Univ, Aaron Diamond AIDS Res Ctr, New York, NY 10016 USA
[2] Katholieke Univ Leuven, Rega Inst Med Res, B-3000 Louvain, Belgium
[3] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
[4] Progen Pharmaceut, Tarrytown, NY 10591 USA
[5] AnorMED, Langley, BC V2Y 1N5, Canada
关键词
D O I
10.1038/nm0198-072
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 bicyclam AMD3100 (formula weight 830) blocks HIV-1 entry and membrane fusion via the CXCR4 co-receptor, but not via CCR5. AMD3100 prevents monoclonal antibody 12G5 from binding to CXCR4 but has no effect on binding of monoclonal antibody 2D7 to CCR5. It also inhibits binding of the CXC-chemokine, SDF-1 alpha, to CXCR4 and subsequent signal transduction, bur does not itself cause signaling and has no effect on RANTES signaling via CCR5. Thus, AMD3100 prevents CXCR4 functioning as both a HIV-1 co-receptor and a CXC-chemokine receptor. Development of small molecule inhibitors of HIV-1 entry is feasible.
引用
收藏
页码:72 / 77
页数:6
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