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Boronic acid functionalized fibrous cellulose for the selective enrichment of glycopeptides

Enrichment of glycoproteins has been important because of their dynamicity and role in biological systems. Study of glycoproteins is complex because of the simultaneous glycosylation and deglycosylation inside the body. Often employed affinities for glycopeptides are hydrazide, boronic acid, or phys...

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Published in:Journal of separation science 2020-04, Vol.43 (7), p.1348-1355
Main Authors: Sajid, Muhammad Salman, Jabeen, Fahmida, Hussain, Dilshad, Gardner, Qurra‐tul‐Ann Afza, Ashiq, Muhammad Naeem, Najam‐ul‐Haq, Muhammad
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cited_by cdi_FETCH-LOGICAL-c4716-3305ba2c96272e5d43b81b951e2b2676141ee8ae8f99475685e3c8c3d83bdb33
cites cdi_FETCH-LOGICAL-c4716-3305ba2c96272e5d43b81b951e2b2676141ee8ae8f99475685e3c8c3d83bdb33
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container_title Journal of separation science
container_volume 43
creator Sajid, Muhammad Salman
Jabeen, Fahmida
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Ashiq, Muhammad Naeem
Najam‐ul‐Haq, Muhammad
description Enrichment of glycoproteins has been important because of their dynamicity and role in biological systems. Study of glycoproteins is complex because of the simultaneous glycosylation and deglycosylation inside the body. Often employed affinities for glycopeptides are hydrazide, boronic acid, or physiosorbed lectin on support materials. Cellulose, a natural polysaccharide, has rich surface chemistry, stable structure, low cost and availability in different variants. In present study, fibrous cellulose is oxidized using periodate to modify with boronic acid. Attachment of boronic acid is confirmed by Fourier transform infrared spectroscopy. Particle size and morphology of boronic acid@fibrous cellulose is studied by scanning electron microscopy. The enrichment efficiency is evaluated by using horseradish peroxidase as model protein. Boronic acid@fibrous cellulose is selective up to 1:250 for spiked horseradish peroxidase in bovine serum albumin digest, sensitive down to 0.1 femtomol and recovering 88.15% glycopeptides. Moreover, protein binding capacity is determined as 213 mg/g and 41% sequence coverage of horseradish peroxidase protein with all eight glycosylation sites detected. Total of 18 glycopeptides are enriched from immunoglobulin digest showing ability of boronic acid@fibrous cellulose to enrich glycoproteins from multiglycoforms. Enrichment from human serum recovers 18% extracellular and 72% secreted glycoproteins via bottom‐up approach and online tools.
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Study of glycoproteins is complex because of the simultaneous glycosylation and deglycosylation inside the body. Often employed affinities for glycopeptides are hydrazide, boronic acid, or physiosorbed lectin on support materials. Cellulose, a natural polysaccharide, has rich surface chemistry, stable structure, low cost and availability in different variants. In present study, fibrous cellulose is oxidized using periodate to modify with boronic acid. Attachment of boronic acid is confirmed by Fourier transform infrared spectroscopy. Particle size and morphology of boronic acid@fibrous cellulose is studied by scanning electron microscopy. The enrichment efficiency is evaluated by using horseradish peroxidase as model protein. Boronic acid@fibrous cellulose is selective up to 1:250 for spiked horseradish peroxidase in bovine serum albumin digest, sensitive down to 0.1 femtomol and recovering 88.15% glycopeptides. 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subjects Acids
Adsorption
Animals
Antibiotics
boronic acid
Boronic Acids - blood
Boronic Acids - chemistry
Boronic Acids - metabolism
Cattle
Cellulose
Cellulose - blood
Cellulose - chemistry
Cellulose - metabolism
Cellulose fibers
Enrichment
Fourier transforms
Glycopeptides
Glycopeptides - blood
Glycopeptides - chemistry
Glycopeptides - metabolism
glycopeptides enrichment
Glycoproteins
Horseradish Peroxidase - metabolism
human serum
Humans
Immunoglobulins - metabolism
mass spectrometry
Morphology
Peroxidase
Polysaccharides
Proteins
Serum albumin
Serum Albumin, Bovine - metabolism
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
title Boronic acid functionalized fibrous cellulose for the selective enrichment of glycopeptides
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