Compact Intermediates in RNA Folding

被引:140
作者
Woodson, Sarah A. [1 ]
机构
[1] Johns Hopkins Univ, TC Jenkins Dept Biophys, Baltimore, MD 21218 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 39 | 2010年 / 39卷
关键词
ribozyme; energy landscape; collapse transition; SAXS; single-molecule FRET; hydroxyl radical footprinting; GROUP-II INTRON; SELF-SPLICING RNA; SECONDARY STRUCTURE REARRANGEMENT; METAL-ION DEPENDENCE; X-RAY-SCATTERING; TETRAHYMENA-RIBOZYME; SINGLE-MOLECULE; HAIRPIN RIBOZYME; TERTIARY INTERACTIONS; CRYSTAL-STRUCTURE;
D O I
10.1146/annurev.biophys.093008.131334
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Large noncoding RNAs fold into their biologically functional structures via compact yet disordered intermediates, which couple the stable secondary structure of the RNA with the emerging tertiary fold. The specificity of the collapse transition, which coincides with the assembly of helical domains, depends on RNA sequence and counterions. It determines the specificity of the folding pathways and the magnitude of the free energy barriers to the ensuing search for the native conformation. By coupling helix assembly with nascent tertiary interactions, compact folding intermediates in RNA also play a crucial role in ligand binding and RNA-protein recognition.
引用
收藏
页码:61 / 77
页数:17
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