An aptamer and Au/Si CCA based SERS sensor for ultra-sensitive detection of Vimentin during EMT in gastric cancer

被引:2
|
作者
Cheng, Lingling [1 ]
Xu, Jianlin [1 ]
Yuan, Hua [2 ]
Zhao, Qihao [3 ]
Yue, Wei [1 ]
Ma, Shuang [1 ]
Lu, Weimin [4 ]
机构
[1] Nanjing Univ Chinese Med, Yancheng TCM Hosp, Dept Gastroenterol, Yancheng, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Yancheng TCM Hosp, Dept Pharm, Yancheng, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Yancheng TCM Hosp Affiliated, Dept Lab Med, Yancheng, Jiangsu, Peoples R China
[4] Nanjing Univ Chinese Med, Affiliated Hosp, Gen Internal Med Dept, Jiangsu Prov Hosp Tradit Chinese Med, Nanjing 210029, Jiangsu, Peoples R China
关键词
Au/Si CCA; epithelial-mesenchymal transition; gastric cancer; surface-enhanced Raman scattering; Vimentin; EPITHELIAL-MESENCHYMAL TRANSITION; IDENTIFICATION; METASTASIS;
D O I
10.3389/fbioe.2023.1310258
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: In this study, a surface-enhanced Raman scattering (SERS) sensor based on a functionalized Au/Si cap-cone array (Au/Si CCA) was constructed using the identity-release strategy to detect Vimentin changes during epithelial-mesenchymal transition (EMT) in gastric cancer (GC).Methods: The periodic structure of Au/Si CCA, which can form "hot spots" with high density and regular arrangement, is a substrate with excellent performance. Au/Si CCA was functionalized with aptamers as the capture substrate, and Au nanocubes (AuNCs) were modified with 5-carboxyfluorescein (5-FAM) labelled complementary strand as SERS probe. The capture substrate and SERS probe were assembled by hybridization, and the SERS signal intensity of 5-FAM was greatly enhanced. The binding of Vimentin to the aptamer resulted in a broken connection between the SERS sensor Au/Si CCA array and AuNCs, which resulted in a decrease in the signal intensity of 5-FAM. The identity-release strategy requires only a simple step of reaction to achieve rapid detection of target proteins, which has clinical practicability.Results: Using this protocol, the concentration of Vimentin in GES-1 cells could be successfully detected, and the detection limit was as low as 4.92 pg/mL. Biological experiments of Vincristine, Oncovin (VCR)-treated GES-1 cells effectively mimicked the EMT process, and Vimentin changes during EMT could be accurately detected by this method.Discussion: This study provides a selective, ultra-sensitive and accurate assay for Vimentin detection, which may provide a means for the future detection of EMT process in GC.
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页数:9
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