清脆的
检测点注意事项
核酸检测
计算生物学
核酸
核酸酶
计算机科学
注意事项
环介导等温扩增
效应器
纳米技术
灵活性(工程)
DNA
生物
数据科学
医学
遗传学
材料科学
数学
细胞生物学
基因
统计
护理部
免疫学
作者
Jeanne Elisabeth van Dongen,Johanna Theodora Wilhelmina Berendsen,Renske D.M. Steenbergen,Rob M.F. Wolthuis,Jan C. T. Eijkel,Loes I. Segerink
标识
DOI:10.1016/j.bios.2020.112445
摘要
With the trend of moving molecular tests from clinical laboratories to on-site testing, there is a need for nucleic acid based diagnostic tools combining the sensitivity, specificity and flexibility of established diagnostics with the ease, cost effectiveness and speed of isothermal amplification and detection methods. A promising new nucleic acid detection method is Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)-associated nuclease (Cas)-based sensing. In this method Cas effector proteins are used as highly specific sequence recognition elements that can be combined with many different read-out methods for on-site point-of-care testing. This review covers the technical aspects of integrating CRISPR/Cas technology in miniaturized sensors for analysis on-site. We start with a short introduction to CRISPR/Cas systems and the different effector proteins and continue with reviewing the recent developments of integrating CRISPR sensing in miniaturized sensors for point-of-care applications. Finally, we discuss the challenges of point-of-care CRISPR sensing and describe future research perspectives.
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