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本文引用的文献

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StreptoTag: a novel method for the isolation of RNA-binding proteins.链霉亲和素标签:一种分离RNA结合蛋白的新方法。
RNA. 1999 Nov;5(11):1509-16. doi: 10.1017/s1355838299991574.
2
Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure.热力学参数对序列依赖性的扩展改进了RNA二级结构的预测。
J Mol Biol. 1999 May 21;288(5):911-40. doi: 10.1006/jmbi.1999.2700.
3
A streptavidin mutant with altered ligand-binding specificity.一种具有改变的配体结合特异性的链霉亲和素突变体。
Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13525-30. doi: 10.1073/pnas.95.23.13525.
4
Purification and characterization of the nuclear RNase P holoenzyme complex reveals extensive subunit overlap with RNase MRP.核酶RNase P全酶复合物的纯化与特性分析揭示了其与RNase MRP在亚基上存在广泛重叠。
Genes Dev. 1998 Jun 1;12(11):1678-90. doi: 10.1101/gad.12.11.1678.
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Approaches to DNA mutagenesis: an overview.DNA诱变方法概述
Anal Biochem. 1997 Dec 15;254(2):157-78. doi: 10.1006/abio.1997.2428.
6
The use of gene fusions to protein A and protein G in immunology and biotechnology.基因与蛋白A和蛋白G的融合在免疫学和生物技术中的应用。
Pathol Biol (Paris). 1997 Jan;45(1):66-76.
7
Purification of a secreted form of recombinant rabies virus glycoprotein: comparison of two affinity tags.重组狂犬病病毒糖蛋白分泌形式的纯化:两种亲和标签的比较。
Protein Expr Purif. 1996 Mar;7(2):183-93. doi: 10.1006/prep.1996.0026.
8
An RNase P RNA subunit mutation affects ribosomal RNA processing.核糖核酸酶P RNA亚基突变影响核糖体RNA加工。
Nucleic Acids Res. 1996 Aug 15;24(16):3158-66. doi: 10.1093/nar/24.16.3158.
9
Mutational analysis of Saccharomyces cerevisiae nuclear RNase P: randomization of universally conserved positions in the RNA subunit.酿酒酵母核酶P的突变分析:RNA亚基中普遍保守位置的随机化
RNA. 1996 May;2(5):441-51.
10
Selection of RNAs that bind to duplex DNA at neutral pH.在中性pH条件下与双链DNA结合的RNA的筛选。
J Mol Biol. 1996 Jun 7;259(2):216-28. doi: 10.1006/jmbi.1996.0314.

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.

DOI:10.1017/s135583820100245x
PMID:11345441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1370116/
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。