Inhibitors of protein-RNA complexation that target the RNA: Specific recognition of human immunodeficiency virus type 1 TAR RNA by small organic molecules

被引:144
作者
Mei, HY
Cui, M
Heldsinger, A
Lemrow, SM
Loo, JA
Sannes-Lowery, KA
Sharmeen, L
Czarnik, AW
机构
[1] Parke Davis Pharmaceut Res, Dept Chem, Ann Arbor, MI 48106 USA
[2] Parke Davis Pharmaceut Res, Dept Therapeut, Ann Arbor, MI 48106 USA
关键词
D O I
10.1021/bi981308u
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
TAR RNA represents an attractive target for the intervention of human immunodeficiency virus type 1 (HIV-1) replication by small molecules. We now describe three small molecule inhibitors of the HIV-1 Tat-TAR interaction that target the RNA, not the protein. The chemical structures and RNA binding characteristics of these inhibitors are unique for each molecule. Results from various biochemical and spectroscopic methods reveal that each of the three Tat-TAR inhibitors recognizes a different structural feature at the bulge, lower stem, or loop region of TAR. Furthermore, one of these Tat-TAR inhibitors has been demonstrated, in cellular environments, to inhibit (a) a TAR-dependent, Tat activated transcription and (b) the replication of HIV-1 in a latently infectious model.
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页码:14204 / 14212
页数:9
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