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MIgGGly (mouse IgG glycosylation analysis) - a high-throughput method for studying Fc-linked IgG N-glycosylation in mice with nanoUPLC-ESI-MS (CROSBI ID 254995)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Zaytseva, Olga ; Jansen, Bas ; Hanić, Maja ; Mrčela, Mia ; Razdorov, Genadij ; Stojković, Ranko ; Erhardt, Julija ; Brizić, Ilija ; Jonjić, Stipan ; Pezer, Marija et al. MIgGGly (mouse IgG glycosylation analysis) - a high-throughput method for studying Fc-linked IgG N-glycosylation in mice with nanoUPLC-ESI-MS // Scientific reports, 8 (2018), 13688, 9. doi: 10.1038/s41598-018-31844-1

Podaci o odgovornosti

Zaytseva, Olga ; Jansen, Bas ; Hanić, Maja ; Mrčela, Mia ; Razdorov, Genadij ; Stojković, Ranko ; Erhardt, Julija ; Brizić, Ilija ; Jonjić, Stipan ; Pezer, Marija ; Lauc, Gordan

engleski

MIgGGly (mouse IgG glycosylation analysis) - a high-throughput method for studying Fc-linked IgG N-glycosylation in mice with nanoUPLC-ESI-MS

Immunoglobulin G (IgG) N-glycosylation is crucial for its effector functions. It is a complex trait, and large sample sets are needed to discover multiple genetic factors that underlie it. While in humans such high-throughput studies of IgG N-glycans became usual, only one has been carried out in mice. Here we describe and validate a method for the relative quantification of IgG Fc-linked N-glycans in a subclassspecific manner using nano-reverse phase liquid chromatography coupled with mass-spectrometry (nanoRP-LC-MS) applied to murine IgG. High-throughput data processing is ensured by the LaCyTools software. We have shown that IgG isolation procedure is the main source of technical variation in the current protocol. The major glycoforms were quantified reliably with coefficients of variation below 6% for all the analytes with relative abundances above 5%. We have applied our method to a sample set of 3 inbred strains: BALB/c, C57BL/6 and C3H and observed differences in subclass-specific and strainspecific N-glycosylation of IgG, suggesting a significant genetic component in the regulation of Fclinked IgG N-glycosylation.

Protein, N-glycosilation, N-glycan, IgG, nanoRP-LC-MS

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Podaci o izdanju

8

2018.

13688

9

objavljeno

2045-2322

10.1038/s41598-018-31844-1

Povezanost rada

Biologija, Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)

Poveznice
Indeksiranost