A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method

This paper describes a combined antigen/antibody immunoassay implemented in a 96-well plate using fluorescent spectroscopic method. First, goat anti-human IgG was used to capture human IgG (model antigen); goat anti-human IgG (Cy3 or FITC) was used to detect the model antigen; a saturating level of...

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Main Author: Yuan-Cheng Cao
Format: Article
Language:English
Published: Hindawi Limited 2015-01-01
Series:Journal of Spectroscopy
Online Access:http://dx.doi.org/10.1155/2015/248504
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spelling doaj-4601c699dd904c299124d1568ff504a92020-11-24T23:00:43ZengHindawi LimitedJournal of Spectroscopy2314-49202314-49392015-01-01201510.1155/2015/248504248504A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent MethodYuan-Cheng Cao0Key Laboratory of Optoelectronic Chemical Materials and Devices of Ministry of Education, Jianghan University, Wuhan 430056, ChinaThis paper describes a combined antigen/antibody immunoassay implemented in a 96-well plate using fluorescent spectroscopic method. First, goat anti-human IgG was used to capture human IgG (model antigen); goat anti-human IgG (Cy3 or FITC) was used to detect the model antigen; a saturating level of model antigen was then added followed by unlabelled goat anti-human IgG (model antibody); finally, Cy3 labelled rabbit anti-goat IgG was used to detect the model antibody. Two approaches were applied to the concomitant assay to analyze the feasibility. The first approach applied FITC and Cy3 when both targets were present at the same time, resulting in 50 ng/mL of the antibody detection limit and 10 ng/mL of antigen detection limit in the quantitative measurements of target concentration, taking the consideration of FRET efficiency of 68% between donor and acceptor. The sequential approach tended to lower the signal/noise (S/N) ratio and the detection of the model antigen (lower than 1 ng/mL) had better sensitivity than the model antibody (lower than 50 ng/mL). This combined antigen/antibody method might be useful for combined detection of antigens and antibodies. It will be helpful to screen for both antigen and antibody particularly in the situations of the multiserotype and high-frequency mutant virus infections.http://dx.doi.org/10.1155/2015/248504
collection DOAJ
language English
format Article
sources DOAJ
author Yuan-Cheng Cao
spellingShingle Yuan-Cheng Cao
A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method
Journal of Spectroscopy
author_facet Yuan-Cheng Cao
author_sort Yuan-Cheng Cao
title A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method
title_short A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method
title_full A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method
title_fullStr A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method
title_full_unstemmed A Model System for Concurrent Detection of Antigen and Antibody Based on Immunological Fluorescent Method
title_sort model system for concurrent detection of antigen and antibody based on immunological fluorescent method
publisher Hindawi Limited
series Journal of Spectroscopy
issn 2314-4920
2314-4939
publishDate 2015-01-01
description This paper describes a combined antigen/antibody immunoassay implemented in a 96-well plate using fluorescent spectroscopic method. First, goat anti-human IgG was used to capture human IgG (model antigen); goat anti-human IgG (Cy3 or FITC) was used to detect the model antigen; a saturating level of model antigen was then added followed by unlabelled goat anti-human IgG (model antibody); finally, Cy3 labelled rabbit anti-goat IgG was used to detect the model antibody. Two approaches were applied to the concomitant assay to analyze the feasibility. The first approach applied FITC and Cy3 when both targets were present at the same time, resulting in 50 ng/mL of the antibody detection limit and 10 ng/mL of antigen detection limit in the quantitative measurements of target concentration, taking the consideration of FRET efficiency of 68% between donor and acceptor. The sequential approach tended to lower the signal/noise (S/N) ratio and the detection of the model antigen (lower than 1 ng/mL) had better sensitivity than the model antibody (lower than 50 ng/mL). This combined antigen/antibody method might be useful for combined detection of antigens and antibodies. It will be helpful to screen for both antigen and antibody particularly in the situations of the multiserotype and high-frequency mutant virus infections.
url http://dx.doi.org/10.1155/2015/248504
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