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RNA适配体与辅因子、氨基酸、药物及氨基糖苷类抗生素形成的复合物中的结构、识别与区分

Structure, recognition and discrimination in RNA aptamer complexes with cofactors, amino acids, drugs and aminoglycoside antibiotics.

作者信息

Patel D J, Suri A K

机构信息

Cellular Biochemistry and Biophysics Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

出版信息

J Biotechnol. 2000 Mar;74(1):39-60. doi: 10.1016/s1389-0352(99)00003-3.

Abstract

Through the use of in vitro selection techniques, a number of RNA aptamers have been selected for their ability to bind ligands with high affinity and specificity. The three-dimensional solution structures of a number of these complexes have been solved within the last 4 years. This review focuses on the structural characterization of the RNA aptamers bound to the cofactors FMN and AMP, the amino acids arginine and citrulline, the drug theophylline and the aminoglycoside antibiotic tobramycin in solution. Analysis of the structural features of these complexes allows the identification of molecular themes in RNA aptamer structure, recognition and discrimination.

摘要

通过使用体外筛选技术,已经筛选出了许多RNA适体,它们能够以高亲和力和特异性结合配体。在过去4年里,已经解析了其中一些复合物的三维溶液结构。本综述重点关注在溶液中与辅因子FMN和AMP、氨基酸精氨酸和瓜氨酸、药物茶碱以及氨基糖苷类抗生素妥布霉素结合的RNA适体的结构特征。对这些复合物结构特征的分析有助于确定RNA适体结构、识别和区分中的分子主题。

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