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CRISPR/Cas系统的单分子视角:靶点搜索、识别与切割

Single-molecule perspectives of CRISPR/Cas systems: target search, recognition, and cleavage.

作者信息

Lee Jeongmin, Jeong Cherlhyun

机构信息

Chemical and Biological Integrative Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792; Department of Life Sciences, Korea University, Seoul 02841, Korea.

Chemical and Biological Integrative Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Korea; Division of Bio-Medical Science & Technology, University of Science and Technology (UST), Seoul 02792, Korea.

出版信息

BMB Rep. 2025 Jan;58(1):8-16. doi: 10.5483/BMBRep.2024-0182.

Abstract

CRISPR/Cas systems have emerged as powerful tools for gene editing, nucleic acid detection, and therapeutic applications. Recent advances in single-molecule techniques have provided new insights into the DNA-targeting mechanisms of CRISPR/ Cas systems, in particular, Types I, II, and V. Here, we review how single-molecule approaches have expanded our understanding of key processes, namely target search, recognition, and cleavage. Furthermore, we focus on the dynamic behavior of Cas proteins, including PAM site recognition and R-loop formation, which are crucial to ensure specificity and efficiency in gene editing. Additionally, we discuss the conformational changes and interactions that drive precise DNA cleavage by different Cas proteins. This mini review provides a comprehensive overview of CRISPR/Cas molecular dynamics, offering conclusive insights into their broader potential for genome editing and biotechnological applications. [BMB Reports 2025; 58(1): 8-16].

摘要

CRISPR/Cas系统已成为基因编辑、核酸检测及治疗应用的强大工具。单分子技术的最新进展为CRISPR/Cas系统(特别是I型、II型和V型)的DNA靶向机制提供了新见解。在此,我们综述单分子方法如何拓展了我们对关键过程的理解,即靶标搜索、识别和切割。此外,我们聚焦于Cas蛋白的动态行为,包括PAM位点识别和R环形成,这对于确保基因编辑的特异性和效率至关重要。此外,我们讨论了驱动不同Cas蛋白精确切割DNA的构象变化和相互作用。本综述全面概述了CRISPR/Cas分子动力学,为其在基因组编辑和生物技术应用中的更广泛潜力提供了确凿见解。[《BMB报告》2025年;58(1): 8 - 16]

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4185/11788531/21603a9ba8bb/bmb-58-1-8-f1.jpg

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