Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection

Immunoprecipitation (IP) and coimmunoprecipitation (co-IP) are key techniques for studying protein-protein interactions. These methods utilize immobilized protein A or protein G to isolate antibody-bound target antigens. The main disadvantage of traditional immunoprecipitation and coimmunoprecipitat...

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Main Authors: M. Walid Qoronfleh, Ling Ren, Daryl Emery, Maria Perr, Barbara Kaboord
Format: Article
Language:English
Published: Hindawi Limited 2003-01-01
Series:Journal of Biomedicine and Biotechnology
Online Access:http://dx.doi.org/10.1155/S1110724303209256
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spelling doaj-fcc981fbfab1484882f4da5c8c58abbb2020-11-25T02:00:33ZengHindawi LimitedJournal of Biomedicine and Biotechnology1110-72431110-72512003-01-012003529129810.1155/S1110724303209256Use of Immunomatrix Methods to Improve Protein-Protein Interaction DetectionM. Walid Qoronfleh0Ling Ren1Daryl Emery2Maria Perr3Barbara Kaboord4Bioresearch Division, Perbio Science, 2202 Norh Bartlett Avenue, Milwaukee 53202-1009, WI, USABioresearch Division, Perbio Science, 2202 Norh Bartlett Avenue, Milwaukee 53202-1009, WI, USABioresearch Division, Perbio Science, 2202 Norh Bartlett Avenue, Milwaukee 53202-1009, WI, USABioresearch Division, Perbio Science, 2202 Norh Bartlett Avenue, Milwaukee 53202-1009, WI, USABioresearch Division, Perbio Science, 2202 Norh Bartlett Avenue, Milwaukee 53202-1009, WI, USAImmunoprecipitation (IP) and coimmunoprecipitation (co-IP) are key techniques for studying protein-protein interactions. These methods utilize immobilized protein A or protein G to isolate antibody-bound target antigens. The main disadvantage of traditional immunoprecipitation and coimmunoprecipitation is that the conditions used to elute the precipitated antigen also release the antibody, contaminating the antigen and destroying the antibody support. To overcome these problems, we describe two methods to generate a reusable antibody support by cross-linking the antibody to immobilized protein A or protein G, or by coupling it directly to the resin. Our studies have demonstrated that the immobilization efficiency for the antibody coupling method was similar for several species of antibody. Furthermore, we illustrate that using both methods of antibody immobilization yields IP and co-IP results similar to traditional protocols but eliminate the antibody heavy and light chains contamination.http://dx.doi.org/10.1155/S1110724303209256
collection DOAJ
language English
format Article
sources DOAJ
author M. Walid Qoronfleh
Ling Ren
Daryl Emery
Maria Perr
Barbara Kaboord
spellingShingle M. Walid Qoronfleh
Ling Ren
Daryl Emery
Maria Perr
Barbara Kaboord
Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection
Journal of Biomedicine and Biotechnology
author_facet M. Walid Qoronfleh
Ling Ren
Daryl Emery
Maria Perr
Barbara Kaboord
author_sort M. Walid Qoronfleh
title Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection
title_short Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection
title_full Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection
title_fullStr Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection
title_full_unstemmed Use of Immunomatrix Methods to Improve Protein-Protein Interaction Detection
title_sort use of immunomatrix methods to improve protein-protein interaction detection
publisher Hindawi Limited
series Journal of Biomedicine and Biotechnology
issn 1110-7243
1110-7251
publishDate 2003-01-01
description Immunoprecipitation (IP) and coimmunoprecipitation (co-IP) are key techniques for studying protein-protein interactions. These methods utilize immobilized protein A or protein G to isolate antibody-bound target antigens. The main disadvantage of traditional immunoprecipitation and coimmunoprecipitation is that the conditions used to elute the precipitated antigen also release the antibody, contaminating the antigen and destroying the antibody support. To overcome these problems, we describe two methods to generate a reusable antibody support by cross-linking the antibody to immobilized protein A or protein G, or by coupling it directly to the resin. Our studies have demonstrated that the immobilization efficiency for the antibody coupling method was similar for several species of antibody. Furthermore, we illustrate that using both methods of antibody immobilization yields IP and co-IP results similar to traditional protocols but eliminate the antibody heavy and light chains contamination.
url http://dx.doi.org/10.1155/S1110724303209256
work_keys_str_mv AT mwalidqoronfleh useofimmunomatrixmethodstoimproveproteinproteininteractiondetection
AT lingren useofimmunomatrixmethodstoimproveproteinproteininteractiondetection
AT darylemery useofimmunomatrixmethodstoimproveproteinproteininteractiondetection
AT mariaperr useofimmunomatrixmethodstoimproveproteinproteininteractiondetection
AT barbarakaboord useofimmunomatrixmethodstoimproveproteinproteininteractiondetection
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