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聚酰胺-胺树枝状大分子抑制Tat肽与TAR RNA的结合。

Polyamidoamine dendrimers inhibit binding of Tat peptide to TAR RNA.

作者信息

Zhao Hong, Li Jinru, Xi Fu, Jiang Long

机构信息

Center for Molecular Science, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100080, PR China.

出版信息

FEBS Lett. 2004 Apr 9;563(1-3):241-5. doi: 10.1016/S0014-5793(04)00284-4.

Abstract

The binding of polyamidoamine (PAMAM) dendrimer or Tat peptide to trans-acting responsive element (TAR) RNA has been studied using microgravimetric quartz crystal microbalance (QCM). Experimental results showed that PAMAM dendrimer could form complexes with TAR RNA. Especially, PAMAM dendrimer could disrupt the interaction of Tat peptide with TAR RNA, which is essential for HIV-1 virus replication, suggesting that QCM is a powerful tool for studying the binding processes of Tat peptide-TAR RNA and drug-TAR RNA and has great significance for the design of new drugs. An equation to measure the binding ability between TAR RNA and other species has been proposed.

摘要

利用微重力石英晶体微天平(QCM)研究了聚酰胺胺(PAMAM)树枝状大分子或Tat肽与反式作用应答元件(TAR)RNA的结合。实验结果表明,PAMAM树枝状大分子可与TAR RNA形成复合物。特别是,PAMAM树枝状大分子可破坏Tat肽与TAR RNA的相互作用,而这种相互作用对HIV-1病毒复制至关重要,这表明QCM是研究Tat肽-TAR RNA和药物-TAR RNA结合过程的有力工具,对新药设计具有重要意义。已提出一个用于测量TAR RNA与其他物质之间结合能力的方程。

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