一种生物素化MutS融合蛋白及其在快速突变筛选技术中的应用

Daniel H. Geschwind , Richard Rhee , Stanley F. Nelson
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引用次数: 19

摘要

大肠杆菌DNA错配修复蛋白MutS在体内和体外结合单碱基对错配和短缺失。为了使该蛋白适用于突变检测,构建了具有生物素化肽结构域的大肠杆菌MutS融合蛋白(MutSb)。生物素化标记有利于亲和素检测和结合MutS,而不会显著改变MutS在体外的DNA错配结合特性。我们描述了一种新的、快速的MutSb突变检测方法,使用链霉亲和素涂覆的磁珠,并证明MutSb也可以用于从溶液中的DNA片段混合物中去除含有错配的DNA片段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A biotinylated MutS fusion protein and its use in a rapid mutation screening technique

The Escherichia coli DNA mismatch repair protein, MutS, binds single base pair mismatches and short deletions in vivo and in vitro. To adapt this protein for mutation detection, a fusion protein of E. coli MutS with a biotinylated peptide domain has been constructed (MutSb). The biotinylation tag facilitates MutS detection and binding by avidin without significantly altering the DNA mismatch binding properties of MutS in vitro. We describe a novel and rapid mutation detection method with MutSb using streptavidin-coated magnetic beads and demonstrate that MutSb can also be used to remove mismatch containing DNA fragments from a mixture of DNA fragments in solution.

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