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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Online Access: | http://dx.doi.org/10.1155/S1110724303209256 |
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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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1724959713737572352 |