| Literature DB >> 17493628 |
Theresa Martinez1, Danielle Pace, Lowell Brady, Mary Gerhart, Alain Balland.
Abstract
This paper describes the analysis of a novel modification identified on the light chain of a recombinant IgG2 antibody. This modification, a +162 Da adduct, suggestive of a single hexose addition, was observed by mass analysis of the reduced molecule. The modification was located on residue serine 66 of the light chain by investigation with LC-MS peptide mapping, mass spectrometry and N-terminal sequencing techniques. Location of the adduct on serine pointed the investigation toward O-linked glycosylation. Identification of the hexose residue was deduced from its elimination by action of alpha-mannosidase, providing evidence for the presence of an O-mannosylated light chain. This type of modification in the glycosylation profile of antibodies, to our knowledge, has not been reported for human IgG molecules.Entities:
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Year: 2007 PMID: 17493628 DOI: 10.1016/j.chroma.2007.04.050
Source DB: PubMed Journal: J Chromatogr A ISSN: 0021-9673 Impact factor: 4.759