Literature DB >> 19892188

Identification, production, and use of polyol-responsive monoclonal antibodies for immunoaffinity chromatography.

Nancy E Thompson1, Katherine M Foley, Elizabeth S Stalder, Richard R Burgess.   

Abstract

Immunoaffinity chromatography is a powerful tool for purification of proteins and protein complexes. The availability of monoclonal antibodies (mAbs) has revolutionized the field of immunoaffinity chromatography by providing a continuous supply of highly uniform antibody. Before the availability of mAbs, the recovery of the target protein from immobilized polyclonal antibodies usually required very harsh, often denaturing conditions. Although harsh conditions are often still used to disrupt the antigen-antibody interaction when using a mAb, various methods have been developed to exploit the uniformity of the antigen-antibody reaction in order to identify agents or conditions that gently disrupt this interaction and thus result in higher recovery of active protein from immunoaffinity chromatography. We discuss here the use of a specific type of monoclonal antibody that we have designated "polyol-responsive monoclonal antibodies" (PR-mAbs). These are naturally occurring mAbs that have high affinity for the antigen under binding conditions, but have low affinity in the presence of a combination of low molecular weight hydroxylated compounds (polyols) and nonchaotropic salts. Therefore, these PR-mAbs can be used for gentle immunoaffinity chromatography. PR-mAbs can be easily identified and adapted to a powerful protein purification method for a target protein.

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Year:  2009        PMID: 19892188     DOI: 10.1016/S0076-6879(09)63028-7

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  7 in total

1.  Production and characterization of monoclonal antibodies to estrogen-related receptor alpha (ERRα) and use in immunoaffinity chromatography.

Authors:  Amanda M Esch; Nancy E Thompson; Jennifer A Lamberski; Janet E Mertz; Richard R Burgess
Journal:  Protein Expr Purif       Date:  2012-05-04       Impact factor: 1.650

2.  Efficient, ultra-high-affinity chromatography in a one-step purification of complex proteins.

Authors:  Marina N Vassylyeva; Sergiy Klyuyev; Alexey D Vassylyev; Hunter Wesson; Zhuo Zhang; Matthew B Renfrow; Hengbin Wang; N Patrick Higgins; Louise T Chow; Dmitry G Vassylyev
Journal:  Proc Natl Acad Sci U S A       Date:  2017-06-12       Impact factor: 11.205

3.  The epitope for the polyol-responsive monoclonal antibody 8RB13 is in the flap-domain of the beta-subunit of bacterial RNA polymerase and can be used as an epitope tag for immunoaffinity chromatography.

Authors:  Elizabeth S Stalder; Lauren H Nagy; Pilar Batalla; Terrance M Arthur; Nancy E Thompson; Richard R Burgess
Journal:  Protein Expr Purif       Date:  2011-01-05       Impact factor: 1.650

4.  Weak protein-protein interactions revealed by immiscible filtration assisted by surface tension.

Authors:  Scott M Berry; Emily N Chin; Shawn S Jackson; Lindsay N Strotman; Mohit Goel; Nancy E Thompson; Caroline M Alexander; Shigeki Miyamoto; Richard R Burgess; David J Beebe
Journal:  Anal Biochem       Date:  2013-11-09       Impact factor: 3.365

Review 5.  Chemical proteomics: terra incognita for novel drug target profiling.

Authors:  Fuqiang Huang; Boya Zhang; Shengtao Zhou; Xia Zhao; Ce Bian; Yuquan Wei
Journal:  Chin J Cancer       Date:  2012-05-23

Review 6.  Challenges and opportunities in the purification of recombinant tagged proteins.

Authors:  Ana Sofia Pina; Christopher R Lowe; Ana Cecília A Roque
Journal:  Biotechnol Adv       Date:  2013-12-12       Impact factor: 14.227

7.  Ms1, a novel sRNA interacting with the RNA polymerase core in mycobacteria.

Authors:  Jarmila Hnilicová; Jitka Jirát Matějčková; Michaela Šiková; Jiří Pospíšil; Petr Halada; Josef Pánek; Libor Krásný
Journal:  Nucleic Acids Res       Date:  2014-09-12       Impact factor: 16.971

  7 in total

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