Isotope labeling strategies for NMR studies of RNA

被引:112
作者
Lu, Kun [1 ,2 ]
Miyazaki, Yasuyuki [1 ,2 ]
Summers, Michael F. [1 ,2 ]
机构
[1] Univ Maryland Baltimore Cty, Howard Hughes Med Inst, Baltimore, MD 21250 USA
[2] Univ Maryland Baltimore Cty, Dept Chem & Biochem, Baltimore, MD 21250 USA
关键词
NMR; RNA structure; Enzymatic ligation; Isotope labeling; SUUM MITOCHONDRIAL TRNA(MET); IN-VITRO TRANSCRIPTION; PRE-MESSENGER-RNA; WEB SERVER; PURIFICATION; ACID; SITE; LIGATION; SEQUENCE; CHROMATOGRAPHY;
D O I
10.1007/s10858-009-9375-2
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 known biological functions of RNA have expanded in recent years and now include gene regulation, maintenance of sub-cellular structure, and catalysis, in addition to propagation of genetic information. As for proteins, RNA function is tightly correlated with structure. Unlike proteins, structural information for larger, biologically functional RNAs is relatively limited. NMR signal degeneracy, relaxation problems, and a paucity of long-range H-1-H-1 dipolar contacts have limited the utility of traditional NMR approaches. Selective isotope labeling, including nucleotide-specific and segmental labeling strategies, may provide the best opportunities for obtaining structural information by NMR. Here we review methods that have been developed for preparing and purifying isotopically labeled RNAs, as well as NMR strategies that have been employed for signal assignment and structure determination.
引用
收藏
页码:113 / 125
页数:13
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