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用于光控CRISPR/Cas编辑的功能可调星形多价CRRNA

Functionally Tunable Star-Shaped Multivalent crRNAs for Photocontrol CRISPR/Cas Editing.

作者信息

Chen Wen-Da, Liu Li, Cheng Liang

机构信息

Beijing National Laboratory for Molecular Sciences (BNLMS), CAS Key Laboratory of Molecular Recognition and Function, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Angew Chem Int Ed Engl. 2025 Apr 14:e202506527. doi: 10.1002/anie.202506527.

Abstract

Clustered regularly interspaced shortpalindromic repeats/CRISPR-associated (CRISPR/Cas)-based genome editing has significantly advanced genetic engineering due to its precision, simplicity, and versatility. However, achieving precise spatial and temporal control remains challenging, restricting therapeutic and research applications. Herein, we introduce a novel class of star-shaped, multivalent crRNAs engineered for precise spatiotemporal control of CRISPR/Cas9 and Cas12a editing systems. These crRNAs are synthesized via single-site chemical modification and can be efficiently purified. By integrating distinct photo-responsive chemical linkages, we achieved selective activation of crRNA activity upon irradiation with specific wavelengths, enabling orthogonal regulation of multiple genetic targets simultaneously. This method demonstrated robust OFF-ON switching capabilities in vitro, characterized by minimal leakage and rapid activation. Importantly, the approach also proved highly effective for temporally controlled gene editing in mammalian cells in vivo, achieving considerable editing efficiency following brief photoactivation. Due to its target sequence-independent, single-site modification design, this strategy may serve as a universal solution for diverse CRISPR/Cas systems, eliminating cumbersome optimization processes. Future advancements incorporating long-wavelength responsive and reversible linkers promise further enhancement of tissue penetration and control, significantly broadening the applicability and impact of this approach in biological research and therapeutic interventions.

摘要

成簇规律间隔短回文重复序列/CRISPR相关蛋白(CRISPR/Cas)介导的基因组编辑因其精确性、简便性和多功能性,极大地推动了基因工程的发展。然而,实现精确的时空控制仍然具有挑战性,限制了其在治疗和研究中的应用。在此,我们引入了一类新型的星形多价crRNA,用于对CRISPR/Cas9和Cas12a编辑系统进行精确的时空控制。这些crRNA通过单点化学修饰合成,并且能够高效纯化。通过整合不同的光响应化学连接,我们实现了在特定波长照射下对crRNA活性的选择性激活,从而能够同时对多个基因靶点进行正交调控。该方法在体外表现出强大的开-关切换能力,具有最小的泄漏和快速激活的特点。重要的是,该方法在体内哺乳动物细胞的时间控制基因编辑中也被证明是非常有效的,在短暂的光激活后实现了可观的编辑效率。由于其与靶序列无关的单点修饰设计,该策略可能为各种CRISPR/Cas系统提供通用解决方案,省去繁琐的优化过程。未来结合长波长响应和可逆连接子的进展有望进一步增强组织穿透和控制能力,显著拓宽该方法在生物学研究和治疗干预中的适用性和影响力。

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