绘制CRISPR碱基编辑器的发展和工程:教训和启示

IF 7.2 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Siyuan Zou , Yihong Sun , Weixin Tang
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引用次数: 0

摘要

CRISPR碱基编辑器(BEs)开启了精确基因组编辑的新篇章。BE发展的短暂而富有成果的历史记录了许多案例研究,这些研究不仅奠定了碱基编辑技术的基础,而且对未来的蛋白质工程工作也有帮助。在这篇综述中,我们总结了各种BEs的开发和工程,并重点介绍了最近的进展。这些包括传统的胞嘧啶和腺嘌呤碱基编辑器(CBEs和abe),新型tada衍生的CBEs,翻转BEs,双重BEs和无crispr的BEs。我们讨论工作流程的每个方面,并强调在工程过程中遇到的成功和挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Charting the development and engineering of CRISPR base editors: lessons and inspirations
CRISPR base editors (BEs) have introduced a new chapter in precise genome editing. The brief but fruitful history of BE development documents many case studies that not only lay the foundation of base-editing technology but are also instrumental to future protein engineering efforts. In this review, we summarize the development and engineering of various BEs with a focus on recent progress. These include traditional cytosine and adenine base editors (CBEs and ABEs), novel TadA-derived CBEs, transversion BEs, dual BEs, and CRISPR-free BEs. We discuss each aspect of the workflow and highlight the successes and challenges encountered in the engineering process.
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来源期刊
Cell Chemical Biology
Cell Chemical Biology Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
14.70
自引率
2.30%
发文量
143
期刊介绍: Cell Chemical Biology, a Cell Press journal established in 1994 as Chemistry & Biology, focuses on publishing crucial advances in chemical biology research with broad appeal to our diverse community, spanning basic scientists to clinicians. Pioneering investigations at the chemistry-biology interface, the journal fosters collaboration between these disciplines. We encourage submissions providing significant conceptual advancements of broad interest across chemical, biological, clinical, and related fields. Particularly sought are articles utilizing chemical tools to perturb, visualize, and measure biological systems, offering unique insights into molecular mechanisms, disease biology, and therapeutics.
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