徐天启,尹芳菲,张晓华,左小磊.化学通报,2020,83(6):497-507.
单碱基多样性的非测序检测
Sequencing-Free Detection of Single Nucleotide Polymorphism
投稿时间:2020-01-09  修订日期:2020-03-02
DOI:
中文关键词:  单碱基多样性  非测序检测  均相检测  原位检测  界面检测
英文关键词:Single nucleotide polymorphism  Sequencing-free detection  Homogenous detection  In situ detection  Interface detection
基金项目:国家自然科学基金项目(81601061,81971093)资助
作者单位E-mail
徐天启 上海交通大学医学院分子医学研究院 上海交通大学医学院附属仁济医院神经外科 上海 200127  
尹芳菲 中国科学院上海应用物理研究所物理生物学研究室 中科院微观界面物理与探测重点实验室 上海 201800
中国科学院大学 北京 100049 
 
张晓华 上海交通大学医学院分子医学研究院 上海交通大学医学院附属仁济医院神经外科 上海 200127 zxh1969@aliyun.com 
左小磊 上海交通大学医学院分子医学研究院 上海交通大学医学院附属仁济医院神经外科 上海 200127 zuoxiaolei@sjtu.edu.cn 
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中文摘要:
      单碱基多样性(SNP)是最常见的基因突变形式之一,经研究证明与很多疾病相关。虽然测序是检测SNP的重要方法,但其需要检测仪器,且检测时间较长,限制了其临床应用。本文综述了SNP的常见非测序分析方法。首先讨论了检测的热力学问题,并归纳了三类主要的检测策略:基于杂交的检测、基于链取代反应的检测和酶介导的检测。在三维均相检测方法中,主要介绍了不同信号开关策略,如荧光开关、酶识别开关和场效应开关。三维原位检测不仅能检测SNP,还能提供其细胞定位信息,在细胞异质性较高时更具优势。二维界面检测的识别反应速率和杂交效率受到一定影响,但界面检测能进一步减小干扰,亦便于实现高通量检测;以DNA正四面体探针界面为代表的改良界面具有优良的灵敏度和特异性。同时,本文亦讨论了现有方法的局限性,并对SNP非测序检测研究进行展望。
英文摘要:
      Single nucleotide polymorphism (SNP) is vastly prevalent in genome mutations, which has been proved to be highly associated with various types of diseases. While sequencing detection plays a vital part in SNP detection, its dependence on equipment and time consumption confines the clinical application. This review focuses on sequencing-free detection of SNP. Thermodynamic aspects are first discussed, followed by major detection strategies:hybridization-based detection, strand displacement reaction, and enzyme-mediated detection. Three categories of detection methods are then elucidated. In three-dimensional homogeneous detection, signal switch strategies such as fluorophore switch, enzyme recognition switch, and field effect switch are elaborated. Three-dimentional detection in situ provides the location of SNP in addition to its presence, showing advantages in SNP detection in heterogeneous cells. In two-dimensional interface detection, despite the compromised reaction rate and hybridization efficiency, the nature of chip detection facilitates multiplexed detection as well as minimized interferences. Corrected chips like DNA tetrahedron-structured probes (TSP) show optimized detection sensitivity and specificity. Setbacks and further research directions in the field are also discussed.
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