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基于CRISPR/Cas9系统的原位生物成像方法进展

Progress of in situ bioimaging methods based on CRISPR/Cas9 system

  • 摘要: 原位生物成像技术为直接观察细胞内核酸或蛋白质生物靶标的定位、表达和相互作用提供了强有力的工具,对于深入理解细胞功能和疾病机制至关重要。CRISPR/Cas9系统作为一种革命性的基因编辑工具,近年来也被用于开发高效的原位成像工具。本文综述了近年来发展的基于Cas9蛋白、工程化单链向导RNA(sgRNA)及其偶联荧光标签的CRISPR/Cas9原位成像方法,并对其在活细胞与固定细胞中的应用特点进行了比较分析。文章重点关注了这些方法的特异性、信号放大效率和多重成像能力,并结合当前的研究进展进行了深入讨论,旨在为基于CRISPR/Cas9系统的原位生物成像技术提供更全面的见解和参考概述,并为相关领域的研究提供参考和指导。

     

    Abstract: In situ bioimaging is a powerful tool for directly observing the localization, expression, and interactions of nucleic acids or protein targets within cells, providing essential insights into cell function and disease mechanisms. In recent years, the CRISPR/Cas9 system, a revolutionary gene-editing tool, has been applied to develop efficient in situ imaging techniques. This paper reviews recent CRISPR/Cas9-based imaging methods utilizing Cas9 protein, engineered single-guide RNA (sgRNA), and coupled fluorescent tags, and compares their application in living and fixed cells. It focuses on the specificity, signal amplification efficiency, and multi-modal imaging capabilities of these methods, with further discussion based on current research, aiming to offer a comprehensive overview of CRISPR/Cas9-based in situ bioimaging techniques, with some valuable reference and guidance for research in related fields.

     

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