Simple and sensitive SERS platform for Staphylococcus aureus one-pot determination by photoactivated CRISPR/Cas12a cascade system and core-shell DNA tetrahedron@AuNP@Fe3O4 reporter

被引:0
作者
Fan, Rui [1 ,2 ]
Luo, Shihua [3 ,6 ]
He, Yangfen [1 ,7 ]
Xiao, Yunju [4 ]
Liang, Yuxin [2 ]
Zhang, Lifeng [1 ,2 ]
Li, Wenbin [2 ]
Zhang, Ye [2 ]
Li, Ling [1 ,5 ]
机构
[1] Guangdong Med Univ, Sch Med Technol, Dongguan 523808, Peoples R China
[2] Southern Med Univ, Guangdong Engn & Technol Res Ctr Rapid Diagnost Bi, Nanfang Hosp,Guangdong Prov Key Lab Single Cell &, Dept Lab Med,Guangdong Prov Key Lab Precis Med Dia, Guangzhou 510515, Peoples R China
[3] Youjiang Med Univ Nationalities, Ctr Clin Lab Diag & Res, Affiliated Hosp, Baise 533000, Guangxi, Peoples R China
[4] Southern Med Univ, Guangdong Prov Peoples Hosp, Guangdong Acad Med Sci, Lab Med, Guangzhou 510080, Peoples R China
[5] Southern Med Univ, Sch Basic Med Sci, Guangzhou 510515, Peoples R China
[6] Youjiang Med Univ Nationalities, Key Lab Res Clin Mol Diag High Incidence Dis Weste, Affiliated Hosp, Guangxi Higher Educ Inst, Baise 533000, Guangxi, Peoples R China
[7] Guangzhou Med Univ, Affiliated Tradit Chinese Med Hosp, Guangzhou 510515, Peoples R China
关键词
Staphylococcus aureus; Catalytic hairpin assembly; Photoactivation; CRISPR/Cas12a; SERS reporter; GOLD NANOPARTICLES; APTAMERS; TAGS;
D O I
10.1007/s00604-025-07098-w
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Staphylococcus aureus (S. aureus) is a widely prevalent Gram-positive bacteria that can cause serious infections and diseases in humans and other organisms. Timely detection and treatment in clinical settings is crucial for patient safety and public health. However, current methods for S. aureus detection still face some limitations, such as time-consuming operation, false positives, and labor-intensive available methodology with low sensitivity. Therefore, it is particularly important to develop a rapid, simple, sensitive, and cost-effective method for detecting S. aureus. We developed a SERS platform based on allosteric aptamer-triggered catalytic hairpin assembly (CHA) and photoactivated CRISPR/Cas12a reactions, combined with a multifunctional core-shell structure as the SERS reporter, enabling highly sensitive one-pot determination of S. aureus. Compared with traditional two-step and one-pot analysis methods, this strategy offers superior sensitivity and can successfully identify real samples contaminated with S. aureus. The platform utilizes light-controlled CHA and CRISPR/Cas12a reactions, effectively preventing interference between different reaction systems. Therefore, the photoactivated one-pot CHA/Cas12a strategy provides a simple, rapid, highly sensitive, specific, and cost-effective method for one-pot determination of S. aureus in clinical samples.
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页数:12
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