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靶向RNA的蛋白质-RNA络合抑制剂:小分子对1型人类免疫缺陷病毒TAR RNA的特异性识别

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

作者信息

Mei H Y, Cui M, Heldsinger A, Lemrow S M, Loo J A, Sannes-Lowery K A, Sharmeen L, Czarnik A W

机构信息

Department of Chemistry, Parke-Davis Pharmaceutical Research, Division of Warner-Lambert Company, Ann Arbor, Michigan 48106, USA.

出版信息

Biochemistry. 1998 Oct 6;37(40):14204-12. doi: 10.1021/bi981308u.

Abstract

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.

摘要

TAR RNA是小分子干预人类免疫缺陷病毒1型(HIV-1)复制的一个有吸引力的靶点。我们现在描述三种靶向RNA而非蛋白质的HIV-1 Tat-TAR相互作用的小分子抑制剂。这些抑制剂的化学结构和RNA结合特性对每个分子来说都是独特的。各种生化和光谱方法的结果表明,这三种Tat-TAR抑制剂中的每一种都能识别TAR凸起、下茎或环区域的不同结构特征。此外,在细胞环境中已证明这些Tat-TAR抑制剂中的一种能够抑制(a)TAR依赖的、Tat激活的转录,以及(b)潜伏感染模型中HIV-1的复制。

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