CATALYTIC ACTIVITY AS A PROBE OF NATIVE RNA FOLDING

被引:15
作者
Wan, Yaqi [1 ]
Mitchell, David, III [1 ]
Russell, Rick [1 ]
机构
[1] Univ Texas Austin, Dept Chem & Biochem, Inst Mol & Cellular Biol, Austin, TX 78712 USA
来源
METHODS IN ENZYMOLOGY, VOL 468: BIOPHYSICAL, CHEMICAL, AND FUNCTIONAL PROBES OF RNA STRUCTURE, INTERACTIONS AND FOLDING, PT A | 2009年 / 468卷
关键词
LIMITING CONFORMATIONAL STEP; SELF-SPLICING RNA; DEAD-BOX PROTEIN; GROUP-I RIBOZYME; TETRAHYMENA RIBOZYME; PERIPHERAL ELEMENT; INTERVENING SEQUENCE; MESSENGER-RNA; KINETIC TRAPS; TRANSCRIPTION;
D O I
10.1016/S0076-6879(09)68010-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As RNAs fold to functional structures, they traverse complex energy landscapes that include many partially folded and misfolded intermediates. For structured RNAs that possess catalytic activity, this activity can provide a powerful means of monitoring folding that is complementary to biophysical approaches. RNA catalysis can be used to track accumulation of the native RNA specifically and quantitatively, readily distinguishing the native structure from intermediates that resemble it and may not be differentiated by other approaches. Here, we outline how to design and interpret experiments using catalytic activity to monitor RNA folding, and we summarize adaptations of the method that have been used to probe aspects of folding well beyond determination of the folding rates.
引用
收藏
页码:195 / 218
页数:24
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