| Literature DB >> 31574255 |
Chengcheng Wu1, Yanke Shan1, Xuping Wu2, Shouyu Wang3, Fei Liu4.
Abstract
Protein detection is a key step in molecular biology research and is required for pathogen and protein marker testing for disease diagnostics. Here, single molecule imaging enzyme-linked immunosorbent assay (iELISA) is proposed to quantitatively measure the porcine circovirus type 2 (PCV2) Cap protein. The monoclonal antibody against PCV2 Cap protein indirectly immobilized on a polyethylene glycol (PEG) passivated slide by biotin-streptavidin interaction is used to capture the PCV2 Cap protein, and the PCV2 Cap protein can be detected in single molecule level according to the fluorescein isothiocyanate (FITC)-labeled secondary antibody using total internal reflection fluorescence microscopy. The single molecule iELISA measurements can be finished within 1 h skipping the time-consuming sample preparation procedures; moreover, it also exhibits excellent protein selectivity and anti-interference capability. With the proposed single molecule iELISA, linear relation between the fluorescent signals and logarithm of target protein concentrations is obtained with the detection limit of 7 ng/mL. Considering its high accuracy in target protein detection with simple procedures and fast speed, it is believed single molecule iELISA can be potentially adopted in fast trace protein detection.Entities:
Keywords: Imaging enzyme-linked immunosorbent assay (iELISA); Porcine circovirus type 2 (PCV2) Cap protein; Protein detection; Single molecule; Total internal reflection fluorescence microscopy
Year: 2019 PMID: 31574255 DOI: 10.1016/j.ab.2019.113466
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365