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HIGH THROUGHPUT ISOLATION AND GLYCOSYLATION ANALYSIS OF IgG – VARIABILITY AND HERITABILITY OF THE IgG GLYCOME IN THREE ISOLATED HUMAN POPULATIONS (CROSBI ID 621035)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Pučić, Maja ; Knežević, Ana ; Vidič, Jana ; Adamczyk, Barbara ; Polašek, Ozren ; Gornik, Olga ; Novokmet, Mislav ; Šupraha-Goreta, Sandra ; Wormald, Mark R ; Redžić, Irma et al. HIGH THROUGHPUT ISOLATION AND GLYCOSYLATION ANALYSIS OF IgG – VARIABILITY AND HERITABILITY OF THE IgG GLYCOME IN THREE ISOLATED HUMAN POPULATIONS. 2012

Podaci o odgovornosti

Pučić, Maja ; Knežević, Ana ; Vidič, Jana ; Adamczyk, Barbara ; Polašek, Ozren ; Gornik, Olga ; Novokmet, Mislav ; Šupraha-Goreta, Sandra ; Wormald, Mark R ; Redžić, Irma ; Campbell, Harry ; Wright, Alan ; Hastie, Nick D ; Wilson, Jim F ; Rudan, Igor ; Wuhrer, Manfred ; Rudd, Pauline M: Josić, Đuro ; Lauc, Gordan

engleski

HIGH THROUGHPUT ISOLATION AND GLYCOSYLATION ANALYSIS OF IgG – VARIABILITY AND HERITABILITY OF THE IgG GLYCOME IN THREE ISOLATED HUMAN POPULATIONS

All immunoglobulin G molecules carryN-glycans, which modulate their biological activity. Changes inN-glycosylation of IgG associate with various diseases and affect the activity of therapeutic antibodies and intravenous immunoglobulins. We have developed a novel 96-well protein G monolithic plate and used it to rapidly isolate IgG from plasma of 2298 individuals from three isolated human populations.N-glycans were released by PNGase F, labeled with 2-aminobenzamide and analyzed by hydrophilic interaction chromatography with fluorescence detection. The majority of the structural features of the IgG glycome were consistent with previous studies, but sialylation was somewhat higher than reported previously. Sialylation was particularly prominent in core fucosylated glycans containing two galactose residues and bisecting GlcNAc where median sialylation level was nearly 80%. Very high variability between individuals was observed, approximately three times higher than in the total plasma glycome. For example, neutral IgG glycans without core fucose varied between 1.3 and 19%, a difference that significantly affects the effector functions of natural antibodies, predisposing or protecting individuals from particular diseases. Heritability of IgG glycans was generally between 30 and 50%. The individual’s age was associated with a significant decrease in galactose and increase of bisecting GlcNAc, whereas other functional elements of IgG glycosylation did not change much with age. Gender was not an important predictor for any IgG glycan. An important observation is that competition between glycosyltransferases, which occursin vitro, did not appear to be relevantin vivo, indicating that the final glycan structures are not a simple result of competing enzymatic activities, but a carefully regulated outcome designed to meet the prevailing physiological needs.

IgG; glycans; variability; heritability; high-throughtput; glycomics

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Podaci o prilogu

2012.

nije evidentirano

objavljeno

Podaci o matičnoj publikaciji

Podaci o skupu

FEBS3+ meeting: From Molecules to life and back

poster

13.06.2012-16.06.2012

Opatija, Hrvatska

Povezanost rada

Temeljne medicinske znanosti