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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Series: | Journal of Spectroscopy |
Online Access: | http://dx.doi.org/10.1155/2015/248504 |
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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 |
work_keys_str_mv |
AT yuanchengcao amodelsystemforconcurrentdetectionofantigenandantibodybasedonimmunologicalfluorescentmethod AT yuanchengcao modelsystemforconcurrentdetectionofantigenandantibodybasedonimmunologicalfluorescentmethod |
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1725641293976043520 |