Detection of in situ cleaved p115 with the cut specific antibodies in rapid protein inactivation system by tobacco etch viral protease cleavage

Antibiotiques Pub Date : 2011-08-10 DOI:10.2147/ANTI.S22825
Mayuko Koreishi, Yasuko Honjo, Ayano Satoh
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引用次数: 1

Abstract

: Gene perturbation methods are commonly used in the study of gene and protein function. The authors of this paper recently developed a rapid protein inactivation technique utilizing tobacco etch virus (TEV)-derived protease. TEV protease recognizes the ENLYFQG (Glu-Asn-Leu-Tyr-Phe-Gln-Gly) amino acid sequence and specifically cleaves between Q and G. The authors developed antibodies that recognize the cleaved TEV (ENLYFQ) sequence, both in vitro and in vivo, but do not bind to uncleaved TEV (ENLYFQG). Using these antibodies, in situ protein cleavage was successfully detected. These antibodies used in combination with the TEV protease may be a useful complement to other perturbation methods.
烟草刻蚀病毒蛋白酶快速蛋白失活系统中原位裂解p115的特异性抗体检测
基因微扰法是研究基因和蛋白质功能的常用方法。作者最近开发了一种利用烟草蚀刻病毒(TEV)衍生蛋白酶的蛋白质快速失活技术。TEV蛋白酶识别ENLYFQG (glu - asn - leu - tyr - ph - gln - gly)氨基酸序列,并特异性地在Q和g之间切割。作者开发了在体外和体内都能识别切割TEV (ENLYFQ)序列的抗体,但不与未切割的TEV (ENLYFQG)结合。使用这些抗体,成功地检测了原位蛋白切割。这些抗体与TEV蛋白酶联合使用可能是对其他扰动方法的有益补充。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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