适体
链霉亲和素
核糖核酸酶P
核糖核蛋白
核糖核酸
生物
核糖核酸酶H
生物化学
生物素
指数富集配体系统进化
分子生物学
计算生物学
基因
作者
Chatchawan Srisawat,David R. Engelke
出处
期刊:RNA
[Cold Spring Harbor Laboratory Press]
日期:2001-04-01
卷期号:7 (4): 632-641
被引量:196
标识
DOI:10.1017/s135583820100245x
摘要
RNA affinity tags would be very useful for the study of RNAs and ribonucleoproteins (RNPs) as a means for rapid detection, immobilization, and purification. To develop a new affinity tag, streptavidin-binding RNA ligands, termed "aptamers," were identified from a random RNA library using in vitro selection. Individual aptamers were classified into two groups based on common sequences, and representative members of the groups had sufficiently low dissociation constants to suggest they would be useful affinity tools. Binding of the aptamers to streptavidin was blocked by presaturation of the streptavidin with biotin, and biotin could be used to dissociate RNA/streptavidin complexes. To investigate the practicality of using the aptamer as an affinity tag, one of the higher affinity aptamers was inserted into RPR1 RNA, the large RNA subunit of RNase P. The aptamer-tagged RNase P could be specifically isolated using commercially available streptavidin-agarose and recovered in a catalytically active form when biotin was used as an eluting agent under mild conditions. The aptamer tag was also used to demonstrate that RNase P exists in a monomeric form, and is not tightly associated with RNase MRP, a closely related ribonucleoprotein enzyme. These results show that the streptavidin aptamers are potentially powerful tools for the study of RNAs or RNPs.
科研通智能强力驱动
Strongly Powered by AbleSci AI