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I-CreI 内切酶及其工程化衍生物:从细胞修饰到基因治疗的应用。

The I-CreI meganuclease and its engineered derivatives: applications from cell modification to gene therapy.

机构信息

Cellectis Genome Surgery, 102 Avenue Gaston Roussel, 93 235 Romainville Cedex, France.

出版信息

Protein Eng Des Sel. 2011 Jan;24(1-2):27-31. doi: 10.1093/protein/gzq083. Epub 2010 Nov 3.

DOI:10.1093/protein/gzq083
PMID:21047873
Abstract

Meganucleases (MNs) are highly specific enzymes that can induce homologous recombination in different types of cells, including mammalian cells. Consequently, these enzymes are used as scaffolds for the development of custom gene-targeting tools for gene therapy or cell-line development. Over the past 15 years, the high resolution X-ray structures of several MNs from the LAGLIDADG family have improved our understanding of their protein-DNA interaction and mechanism of DNA cleavage. By developing and utilizing high-throughput screening methods to test a large number of variant-target combinations, we have been able to re-engineer scores of I-CreI derivatives into custom enzymes that target a specific DNA sequence of interest. Such customized MNs, along with wild-type ones, have allowed for exploring a large range of biotechnological applications, including protein-expression cell-line development, genetically modified plants and animals and therapeutic applications such as targeted gene therapy as well as a novel class of antivirals.

摘要

Meganucleases (MNs) 是高度特异性的酶,可在不同类型的细胞中诱导同源重组,包括哺乳动物细胞。因此,这些酶被用作开发用于基因治疗或细胞系开发的定制基因靶向工具的支架。在过去的 15 年中,来自 LAGLIDADG 家族的几种 MN 的高分辨率 X 射线结构提高了我们对其蛋白-DNA 相互作用和 DNA 切割机制的理解。通过开发和利用高通量筛选方法来测试大量变体-靶组合,我们已经能够将数十种 I-CreI 衍生物重新设计成针对特定感兴趣 DNA 序列的定制酶。这些定制的 MN 与野生型 MN 一起,已经能够探索广泛的生物技术应用,包括蛋白表达细胞系开发、基因修饰动植物以及治疗应用,如靶向基因治疗以及一类新型抗病毒药物。

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The I-CreI meganuclease and its engineered derivatives: applications from cell modification to gene therapy.I-CreI 内切酶及其工程化衍生物:从细胞修饰到基因治疗的应用。
Protein Eng Des Sel. 2011 Jan;24(1-2):27-31. doi: 10.1093/protein/gzq083. Epub 2010 Nov 3.
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Engineered I-CreI derivatives cleaving sequences from the human XPC gene can induce highly efficient gene correction in mammalian cells.工程化的I-CreI衍生物可切割人类XPC基因序列,能在哺乳动物细胞中诱导高效的基因校正。
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