M−CDC: Magnetic pull-down-assisted colorimetric method based on the CRISPR/Cas12a system

•The M−CDC effectively integrates the advantages of CRISPR/Cas12a, magnetic beads-based separation, and AuNP bioprobes.•M−CDC is an easy-to-operated, sensitive, and specific biosensing platform for nucleic acid assay.•The M−CDC has a great potential to be used for large-scale population SARS-CoV-2 s...

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Veröffentlicht in:Methods (San Diego, Calif.) Calif.), 2022-07, Vol.203, p.259-267
Hauptverfasser: Hu, Menglu, Zhu, Debin, Zhou, Xiaoming
Format: Artikel
Sprache:eng
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Zusammenfassung:•The M−CDC effectively integrates the advantages of CRISPR/Cas12a, magnetic beads-based separation, and AuNP bioprobes.•M−CDC is an easy-to-operated, sensitive, and specific biosensing platform for nucleic acid assay.•The M−CDC has a great potential to be used for large-scale population SARS-CoV-2 screening in resource-limited areas. The construction of a rapid, simple, and specific nucleic acid detection platform is of great significance to the control of the large-scale spread of infectious diseases. We have recently established a magnetic pull-down-assisted colorimetric method based on the CRISPR/Cas12a system (termed M−CDC), which effectively integrates the advantages of CRISPR/Cas12a, magnetic beads-based separation, and AuNP bioprobe to provide a simple and specific biosensing platform for nucleic acid assay. The M−CDC method is compatible with point-of-care testing and enables the detection of nucleic acid samples in less than an hour without relying on expensive and complex instruments. In this paper, step-by-step instructions for M−CDC assay, including recombinase polymerase amplification (RPA)/reverse transcription-polymerase chain reaction (RT-RPA) of DNA or RNA, Cas12a-mediated target recognition and cleavage, and subsequent magnetic beads-mediated colorimetric readouts are provided. In addition, the protocol for the expression and purification of Lachnospiraceae bacterium-Cas12a (LbCas12a) protein, the design and synthesis of high-efficient crRNA, and the preparation of AuNP bioprobe are also offered.
ISSN:1046-2023
1095-9130
DOI:10.1016/j.ymeth.2021.11.009