NMR studies of nucleic acid dynamics

被引:33
作者
Al-Hashimi, Hashim M. [1 ]
机构
[1] Univ Michigan, Dept Chem & Biophys, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
RDC; Spin relaxation; Relaxation dispersion; Hoogsteen; Excited states; RESIDUAL DIPOLAR COUPLINGS; MODEL-FREE APPROACH; HIV-1 TAR RNA; HYDROGEN-BONDED COMPLEX; RELAXATION DISPERSION; MAGNETIC-RESONANCE; CRYSTAL-STRUCTURE; CHEMICAL-SHIFTS; INDUCED FIT; TOPOLOGICAL CONSTRAINTS;
D O I
10.1016/j.jmr.2013.08.014
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Nucleic acid structures have to satisfy two diametrically opposite requirements; on one hand they have to adopt well-defined 3D structures that can be specifically recognized by proteins; on the other hand, their structures must be sufficiently flexible to undergo very large conformational changes that are required during key biochemical processes, including replication, transcription, and translation. How do nucleic acids introduce flexibility into their 3D structure without losing biological specificity? Here, I describe the development and application of NMR spectroscopic techniques in my laboratory for characterizing the dynamic properties of nucleic acids that tightly integrate a broad set of NMR measurements, including residual dipolar couplings, spin relaxation, and relaxation dispersion with sample engineering and computational approaches. This approach allowed us to obtain fundamental new insights into directional flexibility in nucleic acids that enable their structures to change in a very specific functional manner. (C) 2013 Published by Elsevier Inc.
引用
收藏
页码:191 / 204
页数:14
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