Multiple-turnover cleavage of double-stranded DNA by sandwiched zinc-finger nuclease.

Yusuke Mineta, Tomoyuki Okamoto, Kosuke Takenaka, Norio Doi, Yasuhiro Aoyama, Takashi Sera
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引用次数: 1

Abstract

To refine zinc-finger nuclease (ZFN) technology, we constructed a sandwiched ZFN, in which a DNA cleavage enzyme was sandwiched with two artificial zinc-finger proteins (AZPs). Because the sandwiched ZFN is designed to cleave the DNA between the two AZP-binding sites, the sandwiched ZFN is expected to bind preferentially to a DNA substrate rather than to cleavage products and thereby cleave it with multiple turnovers. To prove the concept, we sandwiched a staphylococcal nuclease (SNase), which cleaves DNA as a monomer, between two 3-finger AZPs. The AZP-sandwiched SNase cleaved large amounts of dsDNA site-specifically. Such multiple-turnover cleavage was not observed with control nucleases that possess a single AZP.

夹锌指核酸酶对双链DNA的多重翻转切割。
为了进一步完善锌指核酸酶(ZFN)技术,我们构建了一个夹在两个人工锌指蛋白(AZPs)中间的DNA裂解酶。由于夹在中间的ZFN被设计用于在两个azp结合位点之间切割DNA,因此夹在中间的ZFN预计会优先结合DNA底物而不是切割产物,从而通过多次翻转来切割它。为了证明这一概念,我们将葡萄球菌核酸酶(SNase)夹在两个3指azp之间,SNase可以将DNA作为一个单体进行切割。夹在azp中间的SNase特异地切割了大量的dsDNA位点。具有单一AZP的对照核酸酶没有观察到这种多翻转裂解。
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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