Thermodynamics and Kinetics of Adaptive Binding in the Malachite Green RNA Aptamer

被引:21
|
作者
Da Costa, Jason B. [1 ]
Andreiev, Aurelia I. [1 ]
Dieckmann, Thorsten [1 ]
机构
[1] Univ Waterloo, Dept Chem, Waterloo, ON N2L 3G1, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
ISOTHERMAL TITRATION CALORIMETRY; LIGAND-BINDING; CROSS-RELAXATION; RIBOSWITCH; RECOGNITION; FLUORESCENCE; SPECTROSCOPY; SUPPRESSION; POLYMERASE; NETWORKS;
D O I
10.1021/bi400549s
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adaptive binding, the ability of molecules to fold themselves around the structure of a ligand and thereby incorporating it into their three-dimensional fold, is a key feature of most RNA aptamers. The malachite green aptamer (MGA) has been shown to bind several closely related triphenyl dyes with planar and nonplanar structures in this manner. Competitive binding studies using isothermal titration calorimetry and stopped flow kinetics have been conducted with the aim of understanding the adaptive nature of RNA-ligand interaction. The results of these studies reveal that binding of one ligand can reduce the ability of the aptamer pocket to adapt to another ligand, even if this second ligand has a significantly higher affinity to the free aptamer. A similar effect is observed in the presence of Mg2+ ions which stabilize the binding pocket in a more ligand bound-like conformation.
引用
收藏
页码:6575 / 6583
页数:9
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