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一种DNA适配体-精氨酰胺复合物的结构测定与结合动力学

Structure determination and binding kinetics of a DNA aptamer-argininamide complex.

作者信息

Robertson S A, Harada K, Frankel A D, Wemmer D E

机构信息

Department of Chemistry, University of California, Berkeley, California 94720-1460, USA.

出版信息

Biochemistry. 2000 Feb 8;39(5):946-54. doi: 10.1021/bi9915061.

Abstract

The structure of a DNA aptamer, which was selected for specific binding to arginine, was determined using NMR spectroscopy. The sequence forms a hairpin loop, with residues important for binding occurring in the loop region. Binding of argininamide induces formation of one Watson-Crick and two non-Watson-Crick base pairs, which facilitate generation of a binding pocket. The specificity for arginine seems to arise from contacts between the guanidino end of the arginine and phosphates, with atoms positioned by the shape of the pocket. Complex binding kinetics are observed suggesting that there is a slow interconversion of two forms of the DNA, which have different binding affinities. These data provide information on the process of adaptive recognition of a ligand by an aptamer.

摘要

通过核磁共振光谱法确定了一种经筛选可与精氨酸特异性结合的DNA适配体的结构。该序列形成一个发夹环,对结合起重要作用的残基出现在环区域。精氨酰胺的结合诱导形成一个沃森-克里克碱基对和两个非沃森-克里克碱基对,这有助于形成一个结合口袋。对精氨酸的特异性似乎源于精氨酸胍基末端与磷酸根之间的接触,原子由口袋的形状定位。观察到复杂的结合动力学,表明存在两种具有不同结合亲和力的DNA形式的缓慢相互转化。这些数据提供了关于适配体对配体的适应性识别过程的信息。

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