Purification of native and recombinant double-stranded RNA-specific adenosine deaminases

被引:23
作者
O'Connell, MA
Gerber, A
Keegan, LP
机构
[1] Western Gen Hosp, MRC, Human Genet Unit, Edinburgh EH4 2XU, Midlothian, Scotland
[2] Univ Basel, Biozentrum, Dept Cell Biol, CH-4056 Basel, Switzerland
来源
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY | 1998年 / 15卷 / 01期
关键词
D O I
10.1006/meth.1998.0605
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
ADAR1 and ADAR2 are members of a family of enzymes that catalyze the conversion of adenosine to inosine in double-stranded RNA. Unlike the other types of RNA editing that involve multiprotein editing complexes, the site-specific deamination of an adenosine to inosine is catalyzed by single enzymes. ADAR1 and ADAR2 have been purified and the genes cloned from various sources. Each gene encodes multiple splice variants. As it is crucial to have an adequate supply of pure protein to investigate this type of RNA editing, we describe in this article methods for both the purification and the overexpression of either full-length or partial ADAR1 and ADAR2 isoforms. (C) 1998 Academic Press.
引用
收藏
页码:51 / 62
页数:12
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