| Literature DB >> 28116769 |
Zsuzsanna Kovacs1, Adam Simon1, Zoltan Szabo2, Zsolt Nagy3, Laszlo Varoczy4, Ildiko Pal4, Eszter Csanky5, Andras Guttman1,6.
Abstract
Multiple myeloma (MM) is an immedicable malignancy of the human plasma cells producing abnormal antibodies (also referred to as paraproteins) leading to kidney problems and hyperviscosity syndrome. In this paper, we report on the N-glycosylation analysis of paraproteins from total human serum as well as the fragment crystallizable region (Fc ) and fragment antigen binding (Fab ) κ/λ light chain fractions of papain digested immunoglobulins from multiple myeloma patients. CE-LIF detection was used for the analysis of the N-glycans after endoglycosidase (PNGase F) mediated sugar release and fluorophore labeling (APTS). While characteristic N-glycosylation pattern differences were found between normal control and untreated, treated and remission stage multiple myeloma patient samples at the global serum level, less distinctive changes were observed at the immunoglobulin level. Principal component analysis adequately differentiated the four groups (control and three patient groups) on the basis of total serum N-glycosylation analysis. 12 N-glycan features showed statistically significant differences (p <0.05) among various stages of the disease in comparison to the control at the serum level, while only six features were identified with similar significance at the immunoglobulin level, including the analysis of the partitioned Fc fragment as well as the Fab κ and Fab λ chains.Entities:
Keywords: CE-LIF; Multiple myeloma; N-glycans
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Year: 2017 PMID: 28116769 DOI: 10.1002/elps.201700006
Source DB: PubMed Journal: Electrophoresis ISSN: 0173-0835 Impact factor: 3.535