Fürtig Boris, Buck Janina, Manoharan Vijayalaxmi, Bermel Wolfgang, Jäschke Andres, Wenter Philipp, Pitsch Stefan, Schwalbe Harald
Institute for Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance, Johann Wolfgang Goethe-University Frankfurt, Max-von-Laue-Str 7, Frankfurt, Germany.
Biopolymers. 2007;86(5-6):360-83. doi: 10.1002/bip.20761.
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.
如本文所综述,实时核磁共振实验在RNA折叠研究中的应用相对较新。对于许多RNA折叠事件,目前的研究表明时间尺度在秒到分钟范围内。此外,初步研究表明,观察到的一个结构转变的不同折叠速率可能归因于RNA的分级折叠单元。蛋白质折叠核磁共振领域开发的许多实验不能直接应用于RNA:由于RNA的固有交换速率太快,无法在光谱仪外进行氢交换实验,另一方面,弛豫色散实验需要比RNA中观察到的更快的结构转变。另一方面,从时间分辨核磁共振实验中获得的信息,即天然化学位移的获取,可以根据单个长程氢键相互作用的形成很容易地进行解释。结合可以很容易获得的RNA突变数据和进一步提高位点分辨率的新连接技术,时间分辨核磁共振可能成为破译RNA折叠的有力工具。这种理解对于理解细胞中编码和非编码RNA的功能至关重要。