Time-resolved NMR studies of RNA folding

被引:85
|
作者
Fuertig, Boris
Buck, Janina
Manoharan, Vijayalaxmi
Bermel, Wolfgang
Jaeschke, Andres
Wenter, Philipp
Pitsch, Stefan
Schwalbe, Harald
机构
[1] Goethe Univ Frankfurt, Ctr Biomol Magnet Resonance, Inst Organ Chem & Chem Biol, D-60438 Frankfurt, Germany
[2] Bruker Biospin GmbH, D-76287 Rheinstetten, Germany
[3] Heidelberg Univ, Inst Pharm & Mol Biotechnol, Dept Chem, D-69120 Heidelberg, Germany
[4] EPFL BCH, Lab Nucle Acid Chem, CH-1015 Lausanne, Switzerland
关键词
NMR spectroscopy; RNA folding; time-resolved NMR; photolabile caged compounds;
D O I
10.1002/bip.20761
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
The application of real-time NMR experiments to the study of RNA folding, as reviewed in this article, is relatively new. For many RNA folding events, current investigations suggest that the time scales are in the second to minute regime. In addition, the initial investigations suggest that different folding rates are observed for one structural transition may be due to the hierarchical folding units of RNA. Many of the experiments developed in the field of NMR of protein folding cannot directly be transferred to RNA: hydrogen exchange experiments outside the spectrometer cannot be applied since the intrinsic exchange rates are too fast in RNA, relaxation dispersion experiments on the other require faster structural transitions than those observed in RNA. On the other hand, information derived from time-resolved NMR experiments, namely the acquisition of native chemical shifts, can be readily interpreted in light of formation of a single long-range hydrogen bonding interaction. Together with mutational data that can readily be obtained for RNA and new ligation technologies that enhance site resolution even further, time-resolved NMR may become a powerful tool to decipher RNA folding. Such understanding will be of importance to understand the functions of coding and non-coding RNAs in cells. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:360 / 383
页数:24
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