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Core-shell SERS nanotags-based western blot.
Liu, Bing; Tang, Hanyu; Liu, Qian; Wang, Wenwen; Li, Haitao; Zheng, Shiya; Sun, Fei; Zhao, Xiangwei.
Afiliação
  • Liu B; Medical School, Institute of Reproductive Medicine, Nantong University, Nantong, 226001, China. Electronic address: Bingliu88@ntu.edu.cn.
  • Tang H; Medical School, Institute of Reproductive Medicine, Nantong University, Nantong, 226001, China.
  • Liu Q; Medical School, Institute of Reproductive Medicine, Nantong University, Nantong, 226001, China.
  • Wang W; Fudan University Shanghai Cancer Center, Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China; Department of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
  • Li H; Medical School, Institute of Reproductive Medicine, Nantong University, Nantong, 226001, China.
  • Zheng S; Zhongda Hospital, School of Medicine, Southeast University, Nanjing, 210009, China.
  • Sun F; Medical School, Institute of Reproductive Medicine, Nantong University, Nantong, 226001, China. Electronic address: sunfei@ntu.edu.cn.
  • Zhao X; State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, 210096, China; Southeast University Shenzhen Research Institute, Shenzhen, 518000, China. Electronic address: xwzhao@seu.edu.cn.
Talanta ; 253: 123888, 2023 Feb 01.
Article em En | MEDLINE | ID: mdl-36087412
ABSTRACT
Western blot (WB) is the most commonly used scheme for protein identification in life science, but it still faces great challenges in the accurate quantitative detection of low-abundance proteins. Here, we proposed a novel surface-enhanced Raman scattering-based Western blot (SERS-WB) to solve this challenge. SERS nanotags were used as quantitative labels of proteins, which were composed of gold-silver core-shell nanoparticles, and Nile blue A (NBA) molecules were anchored on the interface of the core and shell. The results show that the SERS-WB possessed excellent sensitivity with detection limit of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) protein of 0.15 pg, as well as wide linear dynamic range (LDR) of 382 fg to 382 ng. In addition, the target protein on nitrocellulose (NC) membrane could be directly identified by colorimetric signal due to the aggregation effect of nanoparticles, which greatly simplifies the procedure. This as-proposed strategy will bring new thoughts to technological innovation of WB.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Western Blotting Idioma: En Revista: Talanta Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Western Blotting Idioma: En Revista: Talanta Ano de publicação: 2023 Tipo de documento: Article