Solid-State NMR Spectroscopy of RNA

被引:16
|
作者
Marchanka, Alexander [1 ,2 ]
Carlomagno, Teresa [1 ,2 ,3 ]
机构
[1] Leibniz Univ Hannover, Ctr Biomol Drug Res BMWZ, Hannover, Germany
[2] Leibniz Univ Hannover, Inst Organ Chem, Hannover, Germany
[3] Helmholtz Ctr Infect Res, Grp NMR Based Struct Chem, Braunschweig, Germany
来源
BIOLOGICAL NMR, PT B | 2019年 / 615卷
关键词
HIGH-RESOLUTION; ROTATING SOLIDS; RESONANCE ASSIGNMENT; CROSS-POLARIZATION; AMYLOID FIBRILS; HYDROGEN-BONDS; TAR RNA; PROTEIN; C-13; DYNAMICS;
D O I
10.1016/bs.mie.2018.08.029
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RNA structure is essential to understand RNA function and regulation in cellular processes. RNA acts either in isolation or as part of a complex with proteins. Both isolated and protein-complexed RNA represent a challenge for structural biology, due to the complexity of its conformational space and intrinsic dynamics. NMR, with its capability to cope with dynamic structures, is the optimal technique to study RNA conformation, ideally in solution. However, RNA-protein complexes are often very large, which limits the application of solution-state NMR. In this chapter we describe the methodology that we developed to determine the structure of RNA by solid-state NMR. Solid-state NMR is not limited by large molecular weights and can be optimally applied to study both the RNA and the protein components of large RNA-protein complexes. We review the methods for resonance assignments, collection of RNA-specific distance restraints, as well as detection of protein-RNA interfaces.
引用
收藏
页码:333 / 371
页数:39
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