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Anal Chim Acta ; 1317: 342888, 2024 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-39030018

RESUMO

Rapid and sensitive detection of pathogenic bacteria is crucial for disease prevention and control. The CRISPR/Cas12a system with the DNA cleavage capability holds promise in pathogenic bacteria diagnosis. However, the sensitivity of CRISPR-based assays remains a challenge. Herein, we report a versatile and sensitive pathogen sensing platform (HTCas12a) based on the CRISPR/Cas12a system, hybridization chain reaction (HCR) and Poly T-copper fluorescence nanoprobe. The sensitivity is improved by HCR and the Poly-T-Cu reporter probe reduces the overall experiment cost to less than one dollar per sample. Our results demonstrate the specific recognition of target nucleic acid fragments from other pathogens. Furthermore, a good linear correlation between fluorescence intensity and target quantities were achieved with detection limits of 23.36 fM for Target DNA and 4.17 CFU/mL for S.aureus, respectively. The HTCas12a system offers a universal platform for pathogen detection in various fields, including environmental monitoring, clinical diagnosis, and food safety.


Assuntos
Sistemas CRISPR-Cas , Cobre , Hibridização de Ácido Nucleico , Cobre/química , Poli T/química , Staphylococcus aureus/isolamento & purificação , Staphylococcus aureus/genética , DNA Bacteriano , Limite de Detecção , Corantes Fluorescentes/química , Proteínas de Bactérias , Endodesoxirribonucleases , Proteínas Associadas a CRISPR
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