4.8 Article

Exploring the Trans-Cleavage Activity of CRISPR/Cas12a on Gold Nanoparticles for Stable and Sensitive Biosensing

Journal

ANALYTICAL CHEMISTRY
Volume 93, Issue 11, Pages 4967-4974

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.1c00027

Keywords

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Funding

  1. National Natural Science Foundation of China [21705038, 21974039, 21890744]
  2. National Key R&D Program of China [2019YFA0210100]

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Taking advantage of the trans-cleavage activity of CRISPR/Cas12a on gold nanoparticles, a new spherical nucleic acid (SNA) reporter has been developed for stable and sensitive CRISPR-Dx biosensing. Different trans-cleavage activities of Cas12a systems were discovered on a nanoparticle surface, with LbCas12a highly dependent on DNA strand density and length. The SNA reporter exhibited improved stability and high sensitivity, showing potential for future research in biology science and medical diagnoses.
Taking advantage of the excellent trans-cleavage activity, CRISPR-based diagnostics (CRISPR-Dx) has shown great promise in molecular diagnostics. However, the single-stranded DNA reporter of the current CRISPR-Dx suffers from poor stability and limited sensitivity, which make their application in complex biological environments difficult. Herein, we, for the first time, explore the trans-cleavage activity of CRISPR/Cas12a toward the substrate on gold nanoparticles and apply the new phenomenon to develop a spherical nucleic acid (SNA) reporter for stable and sensitive CRISPR-Dx biosensing. By anchoring the DNA substrate on gold nanoparticles, we discovered different trans-cleavage activities of different types of the Cas12a system (e.g., LbCas12a and AsCas12a) on a nanoparticle surface. The further study suggests that the trans-cleavage activity of LbCas12a on the nanoparticle surface is highly dependent on the density and length of DNA strands. Based on these interesting discoveries, we furthermore develop SNA reporter-based fluorescent CRISPR-Dx for stable and sensitive biosensing application. Compared to traditional ssDNA reporters, the SNA reporter exhibits improved stability, which enables the stable application in a complex serum environment. In addition, the SNA reporter system with tunable density exhibits high sensitivity with a detection limit of 10 fM, which is about 2 orders of magnitude lower than that of the ssDNA reporter system. Finally, the practical application of SNA reporter-based CRISPR-Dx in clinical serum was successfully achieved. These results indicate their significant potential in future research on biology science and medical diagnoses.

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