NUCLEOTIDE ANALOG INTERFERENCE MAPPING

被引:11
|
作者
Suydam, Ian T. [1 ,2 ]
Strobel, Scott A. [1 ,2 ]
机构
[1] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[2] Yale Univ, Dept Chem, New Haven, CT USA
关键词
GROUP-I INTRON; RNASE-P RNA; CRYSTAL-STRUCTURE; TERTIARY CONTACTS; HAIRPIN RIBOZYME; STRUCTURAL BASIS; RIBOSE MOIETIES; CHEMICAL BASIS; ACTIVE-SITE; IDENTIFICATION;
D O I
10.1016/S0076-6879(09)68001-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nucleotide analog interference mapping (NAIM) is a powerful chemogenetic technique that rapidly identifies chemical groups essential for RNA function. Using a series of phosphorothioate-tagged nucleotide analogs, each carrying different modifications of nucleobase or backbone functionalities, it is possible to simultaneously, yet individually, assess the contribution of particular functional groups to an RNA's activity at every position within the molecule. In contrast to traditional mutagenesis, which modifies RNA on the nucleobase level, the smallest mutable unit in a NAIM analysis is a single atom, providing a detailed description of interactions at critical nucteotides. Because the method introduces modified nucteotides by in vitro transcription, NAIM offers a straightforward and efficient approach to study any RNA that has a selectable function, and it can be applied to RNAs of nearly any length.
引用
收藏
页码:3 / 30
页数:28
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