检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:李红招 王浩 尹睿 乐敏[1,2] 李艳 LI Hongzhao;WANG Hao;YIN Rui;YUE Min;LI Yan(Hainan Institute of Zhejiang University,Sanya 572025,Hainan,China;Institute of Preventive Veterinary Sciences/Zhejiang Provincial Key Laboratory of Preventive Veterinary Medicine,College of Animal Sciences,Zhejiang University,Hangzhou 310058,Zhejiang,China)
机构地区:[1]浙江大学海南研究院,海南三亚572025 [2]浙江大学动物科学学院动物预防医学研究所/浙江省动物预防医学重点实验室,浙江杭州310058
出 处:《浙江大学学报(农业与生命科学版)》2023年第5期618-632,共15页Journal of Zhejiang University:Agriculture and Life Sciences
基 金:国家重点研发计划政府间国际科技创新合作项目(2019YFE0103900);国家自然科学基金项目(31872837,32102620);浙江省自然科学基金项目(LZ22C8004);海南省科技计划三亚崖州湾科技城联合项目(2021JJLH0083)。
摘 要:作为一种古老的细菌和古菌免疫系统,规律成簇的间隔短回文重复序列及其相关蛋白[clustered regularly interspaced short palindromic repeats(CRISPR)/CRISPR-associated protein(Cas),CRISPR/Cas]系统现已发展为新兴的热门基因编辑工具,极大地推动了其他多个生物学相关领域的发展。其中,通过结合CRISPR/Cas系统与核酸恒温扩增技术建立了一些新型的高效、灵敏、不依赖仪器设备的检测方法,如DNA内切酶靶向的CRISPR反式报告系统(DNA endonuclease-targeted CRISPR trans-reporter,DETECTR)、特异性高灵敏度的酶报告器系统(specific high-sensitivity enzymatic reporter unlocking,SHERLOCK)等,不但提高了CRISPR/Cas系统在不同应用场景下的检测性能,更进一步激发了其在现场检测中的应用潜力。本文基于近年来被广泛应用的3种CRISPR/Cas系统(CRISPR/Cas9、CRISPR/Cas12a以及CRISPR/Cas13)的生物核酸检测方法,阐述了CRISPR/Cas系统的生物学意义及一般作用原理,并通过回顾以往开展的CRISPR/Cas系统相关的病原检测研究,比较分析了不同检测系统的特点以及在实际应用过程中可能存在的不足,为针对不同病原在不同应用场景下建立更加高效、合理的CRISPR/Cas系统检测方法提供了有益参考。Clustered regularly interspaced short palindromic repeats(CRISPR)/CRISPR-associated protein(Cas)(CRISPR/Cas)system,an ancient bacterial and archaeal immune system,has rapidly developed into a popular gene-editing tool,which largely promotes the development of several biology-related fields.By combining the CRISPR/Cas systems with the isothermal amplification techniques,the novel and effective detection methods with high sensitivity and independence of equipment have been established,such as DNA endonuclease-targeted CRISPR trans-reporter(DETECTR)and specific high-sensitivity enzymatic reporter unlocking(SHERLOCK).These new technologies not only improve the performance of the CRISPR/Cas system in different situations,but also inspire its application potential in the on-site detection.In this review,we summarized the nucleic acid detection methods developed on the three widely-used CRISPR/Cas systems(CRISPR/Cas9,CRISPR/Cas12a,and CRISPR/Cas13),and elucidated their biological significance and the principles of action.We also reviewed the recent studies on the applications of CRISPR/Cas systems in pathogen detection,and analyzed the characteristics and possible defects of different detection systems in practical applications.This review aims to provide more constructive advice on developing adaptable and efficient CRISPR/Cas-based detection methods for different pathogens in various practical scenarios.
关 键 词:CRISPR/Cas系统 Cas蛋白 病原 核酸 检测方法
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.117.121.71