Highly Sensitive Fluoro-Immunosensing for Biomarker Detection Using an Automatic Pipette Tip-Type Biosensing System

• Published in: ACS omega Vol. 4; no. 1; pp. 1487 - 1493
• Main Authors: Takano, Eri, Shimura, Nobuaki, Ujima, Yoshihisa, Sunayama, Hirobumi, Kitayama, Yukiya, Takeuchi, Toshifumi
• Format: Journal Article
• Language: English
• Published: American Chemical Society 01.01.2019
• ISSN: 2470-1343; 2470-1343
• DOI: 10.1021/acsomega.8b02850

An automatic fluorescence detection system based on a pipette tip-type biosensor was developed to detect a prostate-specific antigen (PSA), a biomarker for prostate cancer. Fluorescence-based immunosensing for PSA detection was performed by a sandwich assay with a fluorescence-labeled antibody or its fragments. A small protein A-immobilized reaction plate was placed on a plastic pipette tip (referred to as a Biologi tip). For automatic PSA detection, a programmable dispensing robot equipped with a photodetector was used to suction the samples (i.e., capture antibody, antigen, primary antibody, and reporter molecule), incubation, and migration of the pipette tip to the detection port to measure fluorescence. The use of Fab-fragments and F­(ab′)2-fragments as fluorescently labeled detection antibodies in a sandwich assay resulted in higher signal-to-noise ratios than those for whole IgG. The PSA detection in normal human serum using an Alexa Fluor 647-labeled F­(ab′)2-fragment secondary antibody showed that the fluorescence intensity increased proportionally with PSA concentration, with an estimated detection limit of 1.2 ng/mL. Moreover, 10 pg/mL PSA was detected using an enzymatic reaction with a peroxidase-conjugated F­(ab′)2-fragment secondary antibody and Amplex Red as a substrate. These data indicate that this system is capable of highly sensitive fluorescence-based detection of PSA and suggests the potential for early diagnosis of disease or applications with other biomarkers.