Evaluating RNA Structural Flexibility: Viruses Lead the Way

被引:4
作者
Fairman, Connor W. [1 ]
Lever, Andrew M. L. [2 ]
Kenyon, Julia C. [1 ,2 ]
机构
[1] Univ Cambridge, Homerton Coll, Cambridge CB2 8PH, England
[2] Univ Cambridge, Addenbrookes Hosp, Dept Med, Level 5,Box 157, Cambridge CB2 0QQ, England
来源
VIRUSES-BASEL | 2021年 / 13卷 / 11期
关键词
RNA structure; RNA flexibility; RNA viruses; SHAPE; proximity ligation; NMR; SAXS; smFRET; SECONDARY STRUCTURE; VIRAL-RNA; SHAPE-ANALYSIS; NMR DETECTION; PRINCIPLES; SITES; FRET;
D O I
10.3390/v13112130
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Our understanding of RNA structure has lagged behind that of proteins and most other biological polymers, largely because of its ability to adopt multiple, and often very different, functional conformations within a single molecule. Flexibility and multifunctionality appear to be its hallmarks. Conventional biochemical and biophysical techniques all have limitations in solving RNA structure and to address this in recent years we have seen the emergence of a wide diversity of techniques applied to RNA structural analysis and an accompanying appreciation of its ubiquity and versatility. Viral RNA is a particularly productive area to study in that this economy of function within a single molecule admirably suits the minimalist lifestyle of viruses. Here, we review the major techniques that are being used to elucidate RNA conformational flexibility and exemplify how the structure and function are, as in all biology, tightly linked.
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页数:17
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