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Re-programming DNA-binding specificity in zinc finger proteins for targeting unique address in a genome

机译:重新编程锌指蛋白中的DNA结合特异性以靶向基因组中的唯一地址

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摘要

Recent studies provide a glimpse of future potential therapeutic applications of custom-designed zinc finger proteins in achieving highly specific genomic manipulation. Custom-design of zinc finger proteins with tailor-made specificity is currently limited by the availability of information on recognition helices for all possible DNA targets. However, recent advances suggest that a combination of design and selection method is best suited to identify custom zinc finger DNA-binding proteins for known genome target sites. Design of functionally self-contained zinc finger proteins can be achieved by (a) modular protein engineering and (b) computational prediction. Here, we explore the novel functionality obtained by engineered zinc finger proteins and the computational approaches for prediction of recognition helices of zinc finger proteins that can raise our ability to re-program zinc finger proteins with desired novel DNA-binding specificities.
机译:最近的研究提供了定制设计的锌指蛋白在实现高度特异性基因组操作方面的潜在潜在治疗应用前景。目前,针对锌指蛋白的量身定制的定制设计受到所有可能的DNA靶标识别螺旋信息的可用性的限制。但是,最近的进展表明,设计和选择方法的组合最适合于为已知的基因组靶位点鉴定定制的锌指DNA结合蛋白。可以通过(a)模块化蛋白质工程和(b)计算预测来实现功能齐全的锌指蛋白的设计。在这里,我们探讨了由工程化的锌指蛋白获得的新颖功能以及预测锌指蛋白识别螺旋的计算方法,这些方法可以提高我们以所需的新型DNA结合特异性重新编程锌指蛋白的能力。

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