4.7 Article

Enhanced Colorimetric Immunoassay Accompanying with Enzyme Cascade Amplification Strategy for Ultrasensitive Detection of Low-Abundance Protein

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SCIENTIFIC REPORTS
卷 4, 期 -, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/srep03966

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资金

  1. National 973'' Basic Research Program of China [2010CB732403]
  2. National Natural Science Foundation of China [41176079, 21075019]
  3. Doctoral Program of Higher Education of China [20103514120003]
  4. National Science Foundation of Fujian Province [2011J06003]
  5. China-Russia Bilateral Scientific Cooperation Research Program (NSFC/RFBR) [21211120157]
  6. Program for Changjiang Scholars and Innovative Research Team in University [IRT1116]

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Methods based on enzyme labels have been developed for colorimetric immunoassays, but most involve poor sensitivity and are unsuitable for routine use. Herein, we design an enhanced colorimetric immunoassay for prostate-specific antigen (PSA) coupling with an enzyme-cascade-amplification strategy (ECAS-CIA). In the presence of target PSA, the labeled alkaline phosphatase on secondary antibody catalyzes the formation of palladium nanostructures, which catalyze 3,3',5,5'-tetramethylbenzidine-H2O2 system to produce the colored products, thus resulting in the signal cascade amplification. Results indicated that the ECAS-CIA presents good responses toward PSA, and allows detection of PSA at a concentration as low as 0.05 ng mL(-1). Intra-and inter-assay coefficients of variation are below 9.5% and 10.7%, respectively. Additionally, the methodology is validated for analysis of clinical serum specimens with consistent results obtained by PSA ELISA kit. Importantly, the ECAS-CIA opens a new horizon for protein diagnostics and biosecurity.

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