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trans -Cleavage of the CRISPR-Cas12a-aptamer system for one-step antigen detection

Rapid detection of prostate-specific antigen (PSA) is pivotal for the early screening of prostate cancer (PCa). Here, we devise a one-step, amplification-free fluorescent detection strategy for PSA, employing the trans -cleavage principle of a CRISPR-Cas12a-aptamer system. This method offers a linea...

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Published in:Chemical communications (Cambridge, England) England), 2023-11, Vol.59 (88), p.13151-13154
Main Authors: Fan, Hongxuan, Luo, Shi-hua, Zhu, Ying, Shi, Jiye, Yin, Fangfei, Li, Jiang
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description Rapid detection of prostate-specific antigen (PSA) is pivotal for the early screening of prostate cancer (PCa). Here, we devise a one-step, amplification-free fluorescent detection strategy for PSA, employing the trans -cleavage principle of a CRISPR-Cas12a-aptamer system. This method offers a linear range of 0.31–5 ng mL −1 and a detection limit of 0.16 ng mL −1 . The high-confidence quantification of PSA is demonstrated through the analysis of real samples, effectively distinguishing between PCa patients and healthy individuals.
doi_str_mv 10.1039/d3cc04532c
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subjects Antigens
Cleavage
Fluorescence
title trans -Cleavage of the CRISPR-Cas12a-aptamer system for one-step antigen detection
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