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用 X 射线晶体学研究 TPP 核糖开关的构象变化。

X-Ray Crystallography to Study Conformational Changes in a TPP Riboswitch.

机构信息

Department of Biochemistry and Molecular Pharmacology, New York University Grossman School of Medicine, New York, NY, USA.

出版信息

Methods Mol Biol. 2023;2568:213-232. doi: 10.1007/978-1-0716-2687-0_14.

Abstract

Conformational rearrangements are key to the function of riboswitches. These regulatory mRNA regions specifically bind to cellular metabolites using evolutionarily conserved sensing domains and modulate gene expression via adjacent downstream expression platforms, which carry gene expression signals. The regulation is achieved through the ligand-dependent formation of two alternative and mutually exclusive conformations involving the same RNA region. While X-ray crystallography cannot visualize dynamics of such dramatic conformational rearrangements, this method is pivotal to understand RNA-ligand interaction that stabilize the sensing domain and drive folding of the expression platform. X-ray crystallography can reveal local changes in RNA necessary for discriminating cognate and noncognate ligands. This chapter describes preparation of thiamine pyrophosphate riboswitch RNAs and its crystallization with different ligands, resulting in structures with local conformational changes in RNA. These structures can help to derive information on the dynamics of the RNA essential for specific binding to small molecules, with potential for using this information for developing designer riboswitch-ligand systems.

摘要

构象重排是核糖开关功能的关键。这些调节性 mRNA 区域通过进化上保守的感应结构域特异性地结合细胞代谢物,并通过相邻的下游表达平台调节基因表达,这些平台携带基因表达信号。这种调节是通过配体依赖性形成两种替代的、相互排斥的构象来实现的,涉及相同的 RNA 区域。虽然 X 射线晶体学无法可视化这种剧烈构象重排的动态,但这种方法对于理解稳定感应结构域并驱动表达平台折叠的 RNA-配体相互作用至关重要。X 射线晶体学可以揭示 RNA 中用于区分同源和非同源配体的局部变化。本章描述了硫胺素焦磷酸核糖开关 RNA 的制备及其与不同配体的结晶,导致 RNA 局部构象变化的结构。这些结构可以帮助我们获得有关与小分子特异性结合所需的 RNA 动力学的信息,为开发设计的核糖开关-配体系统提供了潜力。

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