| Literature DB >> 26169135 |
Xiaoyan Guan1, Kyle A Noble2, Yeqing Tao3, Kenneth H Roux2, Shridhar K Sathe4, Nicolas L Young1, Alan G Marshall1,3.
Abstract
The potential epitope of a recombinant food allergen protein, cashew Ana o 1, reactive to monoclonal antibody, mAb 2G4, has been mapped by solution-phase amide backbone H/D exchange (HDX) monitored by Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS). Purified mAb 2G4 was incubated with recombinant Ana o 1 (rAna o 1) to form antigen:monoclonal antibody (Ag:mAb) complexes. Complexed and uncomplexed (free) rAna o 1 were then subjected to HDX-MS analysis. Five regions protected from H/D exchange upon mAb binding are identified as potential conformational epitope-contributing segments.Entities:
Keywords: FTMS; allergen; hydrogen/deuterium exchange; protein complex
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Year: 2015 PMID: 26169135 DOI: 10.1002/jms.3589
Source DB: PubMed Journal: J Mass Spectrom ISSN: 1076-5174 Impact factor: 1.982