| Literature DB >> 32242409 |
Yijuan Bao1, Yongzhong Jiang2,3, Erhu Xiong1, Tian Tian1, Zhenzhen Zhang4, Jing Lv3, Yang Li3, Xiaoming Zhou1.
Abstract
Loop-mediated isothermal amplification (LAMP) is a sensitive and widely used gene amplification technique. However, high amplification efficiency and amplification products containing multiple inverted repeats make the LAMP reaction extremely vulnerable to false-positive amplification caused by contamination. Herein, a contamination-free LAMP (CUT-LAMP) assisted by the CRISPR/Cas9 cleavage with superior reliability and durability has been reported. The core of CUT-LAMP is the engineering of the forward or backward inner primer in the target-independent region, which makes the LAMP products contain a protospacer adjacent motif (PAM) site for the CRISPR/Cas9 recognition. For the CUT-LAMP reaction, cross-contamination can be efficiently cleaved by the corresponding Cas9/sgRNA, but the target gene can get rid of digestion due to the lack of a PAM site near the recognition region. CUT-LAMP shows impressive contamination resistance but does not significantly increase procedure complexity; thus, it represents a simple and versatile toolkit facilitating the adoption by open- and closed-tube detection format.Keywords: CRISPR/Cas; cross-contamination; detection; loop-mediated isothermal amplification; protospacer adjacent motif
Mesh:
Year: 2020 PMID: 32242409 DOI: 10.1021/acssensors.0c00034
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711