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首页> 外文期刊>Journal of Molecular Biology >COMPREHENSIVE CHEMICAL MODIFICATION INTERFERENCE AND NUCLEOTIDE SUBSTITUTION ANALYSIS OF AN RNA PSEUDOKNOT INHIBITOR TO HIV-1 REVERSE TRANSCRIPTASE
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COMPREHENSIVE CHEMICAL MODIFICATION INTERFERENCE AND NUCLEOTIDE SUBSTITUTION ANALYSIS OF AN RNA PSEUDOKNOT INHIBITOR TO HIV-1 REVERSE TRANSCRIPTASE

机译:RNA Pseudoknot抑制剂对HIV-1逆转录酶的综合化学修饰干扰和核苷酸取代分析

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We had previously used in vitro RNA selection techniques to describe a consensus RNA pseudoknot that binds and inhibits HTV-1 reverse transcriptase (HIV-RT). In this work we constructed variants of this consensus pseudoknot in order to evaluate the contributions of individual nucleotide identities and secondary structure to affinity for HIV-RT. We have also used chemical modification of Ligand RNAs to corroborate the predicted structure of the pseudoknot, to discover which modifiable groups are protected from chemical attack when bound to HIV-RT, and to find which modifications interfere with binding to HIV-RT. A novel interference study is presented which involves selection of ligands from a pool created by mixed reagent oligonucleotide synthesis in order to rapidly determine allowed substitutions of 2'-OCH3 groups for the usual 2'-OH group in such RNA ligands. [References: 16]
机译:我们以前曾使用体外RNA选择技术来描述一个共有RNA假结,该假结可结合并抑制HTV-1逆转录酶(HIV-RT)。在这项工作中,我们构建了该共有假结的变体,以评估各个核苷酸身份和二级结构对HIV-RT亲和力的贡献。我们还使用了配体RNA的化学修饰来证实假结的预测结构,以发现与HIV-RT结合时可保护的可修饰基团免受化学攻击,并发现哪些修饰会干扰与HIV-RT的结合。提出了一种新颖的干扰研究,其涉及从混合试剂寡核苷酸合成产生的库中选择配体,以便快速确定2'-OCH3基团在此类RNA配体中通常的2'-OH基团的允许取代。 [参考:16]

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