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激光热激引发的 RNA 发夹环的快速折叠。

Fast folding of RNA pseudoknots initiated by laser temperature-jump.

机构信息

Department of Physics (M/C 273), University of Illinois at Chicago, 845 W. Taylor St., Chicago, Illinois 60607, USA.

出版信息

J Am Chem Soc. 2011 Nov 23;133(46):18767-74. doi: 10.1021/ja205737v. Epub 2011 Nov 1.

Abstract

RNA pseudoknots are examples of minimal structural motifs in RNA with tertiary interactions that stabilize the structures of many ribozymes. They also play an essential role in a variety of biological functions that are modulated by their structure, stability, and dynamics. Therefore, understanding the global principles that determine the thermodynamics and folding pathways of RNA pseudoknots is an important problem in biology, both for elucidating the folding mechanisms of larger ribozymes as well as addressing issues of possible kinetic control of the biological functions of pseudoknots. We report on the folding/unfolding kinetics of a hairpin-type pseudoknot obtained with microsecond time-resolution in response to a laser temperature-jump perturbation. The kinetics are monitored using UV absorbance as well as fluorescence of extrinsically attached labels as spectroscopic probes of the transiently populated RNA conformations. We measure folding times of 1-6 ms at 37 °C, which are at least 100-fold faster than previous observations of very slow folding pseudoknots that were trapped in misfolded conformations. The measured relaxation times are remarkably similar to predictions of a computational study by Thirumalai and co-workers (Cho, S. S.; Pincus, D.L.; Thirumalai, D. Proc. Natl. Acad. Sci. U. S. A. 2009, 106, 17349-17354). Thus, these studies provide the first observation of a fast-folding pseudoknot and present a benchmark against which computational models can be refined.

摘要

RNA 假结是 RNA 中具有三级相互作用的最小结构基序的示例,可稳定许多核酶的结构。它们在多种生物功能中也起着至关重要的作用,这些功能受其结构、稳定性和动力学的调节。因此,理解决定 RNA 假结热力学和折叠途径的全局原则是生物学中的一个重要问题,这对于阐明较大核酶的折叠机制以及解决假结生物功能的可能动力学控制问题都很重要。我们报告了在微秒时间分辨率下,通过激光温度跃变扰动获得的发夹型假结的折叠/解折叠动力学。动力学通过紫外吸收以及外部附着标记的荧光来监测,作为瞬态 RNA 构象的光谱探针。我们在 37°C 下测量的折叠时间为 1-6ms,比以前观察到的非常缓慢折叠的假结快至少 100 倍,这些假结被困在错误折叠的构象中。测量的弛豫时间与 Thirumalai 及其同事的计算研究(Cho,SS;Pincus,DL;Thirumalai,D.Proc Natl Acad Sci USA 2009,106,17349-17354)的预测非常相似。因此,这些研究首次观察到快速折叠的假结,并提供了一个基准,可据此改进计算模型。

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