4.7 Article

Aptamer-based novel Ag-coated magnetic recognition and SERS nanotags with interior nanogap biosensor for ultrasensitive detection of protein biomarker

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 334, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.129640

关键词

SERS tag; Novel magnetic capture; Aptamer recognition; C-reactive protein; Biomarker detection

资金

  1. National Natural Science Foundation of China [81773684, 81872759, 82003707]
  2. Guangdong Natural Science Funds for Distinguished Young Scholars [2018B030306033]
  3. Pearl River S&T Nova Program of Guangzhou [201806010060]
  4. Pearl River Talent Program [2017GC010363]
  5. Basic and Applied Basic Research Foundation of Guangdong Province [2020A1515110436]
  6. China Postdoctoral Science Foundation [2020M673087]

向作者/读者索取更多资源

A novel aptamer SERS biosensor for highly sensitive protein biomarker detection was developed, achieving a limit of detection of 10 fM for C-reactive protein. The biosensor exhibited excellent selectivity and specificity for CRP, and high accuracy in the detection of actual human serum samples, showing great promise for clinical diagnosis of diseases.
The design of a rapid, simple, and ultrasensitive detection platform of protein biomarkers has become an urgent need in early diagnosis and treatment. Surface-enhanced Raman scattering (SERS) technology, with the unique advantages of ultra-sensitivity and fingerprint recognition, has attracted much attention in biomarker detection. An innovative aptamer SERS biosensor for highly sensitive protein biomarker detection was presented. This biosensor contains a SERS tag (reporter-labeled Au nano-bridged nanogaps particles, Au NNPs) and novel magnetic capture substrate (Ag-coated Fe3O4-Au NPs, Ag MNPs). C-reactive protein (CRP), a representative biomarker for diagnosing, was used to assess the SERS performance of this biosensor. Aptamers against CRP were modified on both SERS tag and magnetic capture substrate for specific recognition by Au NNPs-CRP-Ag MNPs sandwich assay. This strategy achieved sensitive detection of CRP with a limit of detection (LOD) of 10 fM (1.14 pg/mL), and is much lower than reported analytical methods. Besides, this method exhibits excellent selectivity and specificity for CRP under the interference of other proteins and displays high accuracy in the detection of actual human serum samples. This proposed detection strategy can be extended to the sensitive detection of other biomarker proteins and hold great promise in the clinical diagnosis of diseases.

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