Development of a phage display-mediated immunoassay for the detection of vascular endothelial growth factor.

Anal Bioanal Chem

Department of Biochemistry, Faculty of Biological Sciences, Tarbiat Modares University, Jalal Ale Ahmad Highway, Tehran, 14115-154, Iran.

Published: November 2020

AI Article Synopsis

  • VEGF is a key biomarker in cancer due to its role in angiogenesis and is often elevated in early cancer stages.
  • Researchers developed an innovative immunoassay using phage display and PCR (PD-IPCR) to detect VEGF more sensitively, achieving a detection limit as low as 3 pg/ml.
  • The method demonstrated strong correlation with conventional ELISA testing in clinical samples, indicating its potential for accurate VEGF detection in human serum.

Article Abstract

Because of the critical role of vascular endothelial growth factor (VEGF) in angiogenesis and its significantly increased serum levels in early stages of cancer, VEGF is considered an important prognostic biomarker in different cancers. Herein, the amplification power of PCR combined with phage displaying anti-VEGF VHH, a sensitive real-time immunoassay, was precisely designed based on phage display-mediated immuno-PCR (PD-IPCR) for the detection of VEGF. This system benefits from strong and specific binding of antigen and antibody in a sandwich immunosorbent assay platform using avastin (anti-VEGF monoclonal antibody) as the capture antibody. The anti-VEGF phage particles were used as both anti-VEGF agent and DNA template in the PD-IPCR. Anti-VEGF phage ELISA showed a linear range of 3-250 ng/ml and a limit of detection (LOD) of 1.1 ng/ml. Using the PD-IPCR method, the linear range of VEGF detection was found to be 0.06-700 ng/ml, with a detection limit of 3 pg/ml. The recovery rate in serum ranged from 83% to 99%, with a relative standard deviation of 1.2-4.9%. These values indicate that the method has good sensitivity for use in clinical analysis. The proposed method was successfully applied to the clinical determination of VEGF in human serum samples, and the results showed excellent correlation with conventional ELISA (R = 0.995). The novel immunoassay provides a specific and sensitive immunoassay protocol for VEGF detection at very low levels. Graphical abstract.

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Source
http://dx.doi.org/10.1007/s00216-020-02901-4DOI Listing

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