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Rapid acidification and alkylation: Redox analysis of the MHC class I pathway

Powis, S. J., Nesbeth, D., Lenart, I., Fussell, H., Lamb, T., Gould, K. and Antoniou, A. N. (2009) Rapid acidification and alkylation: Redox analysis of the MHC class I pathway. Journal of Immunological Methods, 340 (1). pp. 81-85. ISSN 0022-1759

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To link to this item DOI: 10.1016/j.jim.2008.09.006

Abstract/Summary

The technique of rapid acidification and alkylation can be used to characterise the redox status of oxidoreductases, and to determine numbers of free cysteine residues within substrate proteins. We have previously used this method to analyse interacting components of the MHC class I pathway, namely ERp57 and tapasin. Here, we have applied rapid acidification alkylation as a novel approach to analysing the redox status of MHC class I molecules. This analysis of the redox status of the MHC class I molecules HLA-A2 and HLA-B27, which is strongly associated with a group of inflammatory arthritic disorders referred to as Spondyloarthropathies, revealed structural and conformational information. We propose that this assay provides a useful tool in the study of in vivo MHC class I structure. (c) 2008 Elsevier B.V. All rights reserved.

Item Type:Article
Refereed:Yes
Divisions:Faculty of Life Sciences > School of Biological Sciences
ID Code:9684
Uncontrolled Keywords:MHC class I, Redox, Alkylation, Oxidoreductases, MAJOR HISTOCOMPATIBILITY COMPLEX, PEPTIDE-LOADING COMPLEX, TRANSGENIC, RATS, ERP57, HLA-B27

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