Engineered Cys 2 His 2 zinc finger DNA-binding domains

A. S. Hirsh, J. Joung
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引用次数: 3

Abstract

Gene therapy reagents such as artificial transcription factors and site-specific endonucleases require "made-to-order" DNA-binding domains with high affinity and specificity for novel target sequences. Cys2His2 zinc finger proteins are the best understood and most commonly used framework for design and selection of such domains. Though a number of design strategies have been described in the literature, they vary significantly in their reliability and ease of execution. This situation has made it difficult for the non-specialist researcher to know how best to construct zinc finger proteins for their application of interest. This article reviews the current state of the technology and its limitations, and discusses prospects for improving our ability to make customized DNA-binding modules.
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设计cys2 His 2锌指dna结合域
基因治疗试剂,如人工转录因子和位点特异性内切酶,需要“按顺序制造”的dna结合域,对新的靶序列具有高亲和力和特异性。Cys2His2锌指蛋白是设计和选择这类结构域的最容易理解和最常用的框架。虽然文献中描述了许多设计策略,但它们在可靠性和执行的便利性方面差异很大。这种情况使得非专业研究人员很难知道如何最好地构建锌指蛋白以用于他们感兴趣的应用。本文综述了该技术的现状及其局限性,并讨论了提高我们定制dna结合模块能力的前景。
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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