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Enhanced CRISPR/Cas12a-based quantitative detection of nucleic acids using double emulsion droplets.

Authors :
Zhang, Yang
Liu, Hangrui
Nakagawa, Yuta
Nagasaka, Yuzuki
Ding, Tianben
Tang, Shi-Yang
Yalikun, Yaxiaer
Goda, Keisuke
Li, Ming
Source :
Biosensors & Bioelectronics. Aug2024, Vol. 257, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

Pairing droplet microfluidics and CRISPR/Cas12a techniques creates a powerful solution for the detection and quantification of nucleic acids at the single-molecule level, due to its specificity, sensitivity, and simplicity. However, traditional water-in-oil (W/O) single emulsion (SE) droplets often present stability issues, affecting the accuracy and reproducibility of assay results. As an alternative, water-in-oil-in-water (W/O/W) double emulsion (DE) droplets offer superior stability and uniformity for droplet digital assays. Moreover, unlike SE droplets, DE droplets are compatible with commercially available flow cytometry instruments for high-throughput analysis. Despite these advantages, no study has demonstrated the use of DE droplets for CRISPR-based nucleic acid detection. In our study, we conducted a comparative analysis to assess the performance of SE and DE droplets in quantitative detection of human papillomavirus type 18 (HPV18) DNA based on CRISPR/Cas12a. We evaluated the stability of SEs and DEs by examining size variation, merging extent, and content interaction before and after incubation at different temperatures and time points. By integrating DE droplets with flow cytometry, we achieved high-throughput and high-accuracy CRISPR/Cas12a-based quantification of target HPV18 DNA. The DE platform, when paired with CRISPR/Cas12a and flow cytometry techniques, emerges as a reliable tool for absolute quantification of nucleic acid biomarkers. • Double emulsion (DE) droplets show enhanced stability in CRISPR/Cas12a-based DNA detection than single emulsion droplets. • The remarkable stability of DE droplets prevents content mixing, reducing contamination risks during incubation. • DE droplets significantly minimize sample loss during encapsulation and incubation, outperforming SE droplets. • DE droplets, compatible with flow cytometry, enable precise and high-throughput CRISPR/Cas12a-based DNA quantification. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09565663
Volume :
257
Database :
Academic Search Index
Journal :
Biosensors & Bioelectronics
Publication Type :
Academic Journal
Accession number :
177065004
Full Text :
https://doi.org/10.1016/j.bios.2024.116339