抗HCV- ns3解旋酶RNA适体的体外筛选及其与HCV 3'(+)UTR的结构相似性

Satoshi Nishikawa, Fumiko Nishikawa, Kotaro Fukuda
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引用次数: 7

摘要

为了筛选和研究抗HCV NS3解旋酶结构域的RNA适体,我们使用N30H和N30V两种RNA池进行了体外筛选。经过8个选择周期,从N30H池中获得的RNA适体在茎环区域具有5'延伸单链区域和保守序列[5'-GGA(U/C)GGAGCC-3']。另一方面,从另一个RNA适配体库N30V中获得的RNA适配体具有3'长的单链区域,具有多个茎环结构。这些适体对解旋酶活性均有较强的抑制作用,其中#5的Kd值为20 nM, IC50值约为50 nM。有趣的是,这些RNA适配体显示出类似的二级结构构型,具有正链3'非翻译区[3'(+)UTR]。已知HCV的3'UTR对HCV的复制很重要,并且与NS3蛋白有很强的亲和力。我们将讨论NS3和3'(+)UTR的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro selection of RNA aptamers against HCV-NS3 helicase and their structural similarity with 3'(+)UTR of HCV.

In order to screen and study of RNA aptamers against HCV NS3 helicase domain, we performed in vitro selection using two kinds of RNA pools, N30H and N30V. After eight selection cycles, RNA aptamers obtained from N30H pool possessed 5' extended single-stranded regions and the conserved sequence [5'-GGA(U/C)GGAGCC-3'] at stem-loop regions. On the other hand RNA aptamers obtained from another pool, N30V, possessed 3' long single-stranded regions with several stem-loop structures. All these aptamers showed strong inhibition of helicase activity in vitro, especially #5 represented Kd = 20 nM and IC50 approximately 50 nM. Interestingly these RNA aptamers showed similar secondary structural configuration with positive-stranded 3' untranslated region [3'(+)UTR]. It is known that 3'UTR of HCV is important for replication of HCV and also has strong affinity with NS3 protein. We will discuss the interaction of NS3 and 3'(+)UTR.

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