清脆的
生物传感器
纳米技术
计算生物学
生物
基因
遗传学
材料科学
作者
Mindong Liang,Zilong Li,Weishan Wang,Jiakun Liu,Leshi Liu,Guoliang Zhu,Loganathan Karthik,Man Wang,Kefeng Wang,Zhong Wang,Jing Yu,Yuting Shuai,Jiaming Yu,Lu Zhang,Zhiheng Yang,Chuan Li,Qian Zhang,Tong Shi,Liming Zhou,Feng Xie
标识
DOI:10.1038/s41467-019-11648-1
摘要
Besides genome editing, CRISPR-Cas12a has recently been used for DNA detection applications with attomolar sensitivity but, to our knowledge, it has not been used for the detection of small molecules. Bacterial allosteric transcription factors (aTFs) have evolved to sense and respond sensitively to a variety of small molecules to benefit bacterial survival. By combining the single-stranded DNA cleavage ability of CRISPR-Cas12a and the competitive binding activities of aTFs for small molecules and double-stranded DNA, here we develop a simple, supersensitive, fast and high-throughput platform for the detection of small molecules, designated CaT-SMelor (CRISPR-Cas12a- and aTF-mediated small molecule detector). CaT-SMelor is successfully evaluated by detecting nanomolar levels of various small molecules, including uric acid and p-hydroxybenzoic acid among their structurally similar analogues. We also demonstrate that our CaT-SMelor directly measured the uric acid concentration in clinical human blood samples, indicating a great potential of CaT-SMelor in the detection of small molecules.
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