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链霉亲和素适体:用于RNA和核糖核蛋白研究的亲和标签。

Streptavidin aptamers: affinity tags for the study of RNAs and ribonucleoproteins.

作者信息

Srisawat C, Engelke D R

机构信息

Department of Biological Chemistry, The University of Michigan, Ann Arbor 48109-0606, USA.

出版信息

RNA. 2001 Apr;7(4):632-41. doi: 10.1017/s135583820100245x.

Abstract

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.

摘要

RNA亲和标签对于RNA和核糖核蛋白(RNP)的研究将非常有用,可作为快速检测、固定和纯化的手段。为了开发一种新的亲和标签,利用体外筛选从随机RNA文库中鉴定出与链霉亲和素结合的RNA配体,即“适体”。根据共同序列将各个适体分为两组,这些组的代表性成员具有足够低的解离常数,表明它们将是有用的亲和工具。链霉亲和素与生物素预饱和会阻断适体与链霉亲和素的结合,生物素可用于解离RNA/链霉亲和素复合物。为了研究将适体用作亲和标签的实用性,将一种亲和力较高的适体插入核糖核酸酶P的大RNA亚基RPR1 RNA中。带有适体标签的核糖核酸酶P可以使用市售的链霉亲和素琼脂糖特异性分离,并且在温和条件下使用生物素作为洗脱剂时可以以催化活性形式回收。适体标签还用于证明核糖核酸酶P以单体形式存在,并且与密切相关的核糖核蛋白酶核糖核酸酶MRP没有紧密关联。这些结果表明,链霉亲和素适体可能是研究RNA或RNP的强大工具。

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