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A Pragmatic Guide to Enrichment Strategies for Mass Spectrometry–Based Glycoproteomics

Authors :
Sharon J. Pitteri
Carolyn R. Bertozzi
Nicholas M. Riley
Source :
Molecular & Cellular Proteomics : MCP
Publication Year :
2021
Publisher :
Elsevier BV, 2021.

Abstract

Glycosylation is a prevalent, yet heterogeneous modification with a broad range of implications in molecular biology. This heterogeneity precludes enrichment strategies that can be universally beneficial for all glycan classes. Thus, choice of enrichment strategy has profound implications on experimental outcomes. Here we review common enrichment strategies used in modern mass spectrometry–based glycoproteomic experiments, including lectins and other affinity chromatographies, hydrophilic interaction chromatography and its derivatives, porous graphitic carbon, reversible and irreversible chemical coupling strategies, and chemical biology tools that often leverage bioorthogonal handles. Interest in glycoproteomics continues to surge as mass spectrometry instrumentation and software improve, so this review aims to help equip researchers with the necessary information to choose appropriate enrichment strategies that best complement these efforts.<br />Graphical Abstract<br />Highlights • Glycosylation is complex and often requires enrichment prior to analysis • Review of common enrichment strategies for mass spectrometry–based glycoproteomics • Enrichment methods have practical considerations and experimental implications • Appropriate enrichment strategies will complement developments in mass spectrometry<br />In Brief Interest in mass spectrometry–based glycoproteomics analysis is increasing because of recent advances in instrumentation and data analysis tools. Such studies can provide a wealth of information across a wide spectrum of glycan classes and biological systems. However, many studies require the choice of an enrichment strategy for glycosylated species prior to analysis to obtain the maximum amount of analytical information. Here, common enrichment strategies are reviewed with strengths and weaknesses, and the practical considerations for various methods are discussed.

Subjects

Subjects :
Proteomics
SAX, strong anion exchange
Special Issue: Glycoproteomics
enrichment
Glycosylation
Computer science
DIA, data-independent acquisition
ConA, concanavalin A
Review
PTMs, post-translational modifications
Biochemistry
Mass Spectrometry
Analytical Chemistry
ETD, electron transfer dissociation
IMAC, immobilized metal affinity chromatography
ManNAz, N-azidoacetylmannosamine
ZIC-HILIC, zwitterionic HILIC
Lectins
Data-independent acquisition
Glycomics
Siglecs, sialic acid–binding immunoglobulin-type lectins
WAX, weak anion exchange
Chromatography
0303 health sciences
030302 biochemistry & molecular biology
glycopeptides
PGC, porous graphitic carbon
Glycoproteomics
Graphitic carbon
Graphite
M6P, mannose-6-phosphate
strong anion exchange electrostatic repulsion hydrophilic interaction chromatography (SAX-ERLIC)
ECD, electron capture dissociation
Glycoside Hydrolases
Ion-mobility spectrometry
WGA, wheat germ agglutinin
Chemical biology
chemical biology
Computational biology
Mass spectrometry
affinity chromatography
HILIC, hydrophilic interaction chromatography
03 medical and health sciences
Animals
Humans
glycoproteomics
Molecular Biology
hydrophilic interaction chromatography (HILIC)
Glycoproteins
030304 developmental biology
AAL, Aleuria aurantia lectin
SPE, solid-phase extraction
AX, anion exchange
IMS, ion mobility spectrometry
MOAC, metal oxide affinity chromatography
LAC, lectin affinity chromatography
Neu5Gc, N-glycolylneuraminic acid
Neu5Ac, N-acetylneuraminic acid
RCA, ricinus communis agglutinin
Chemical coupling
MS, mass spectrometry
HCD, higher-energy collisional dissociation
M-LAC, multi-lectin affinity chromatography
GalT1, β-1,4-galactosyltransferase 1
Bioorthogonal chemistry
CuAAC, i.e., “click” chemistry, copper-catalyzed azide-alkyne cycloadditions
SPAAC, i.e., “copper-free click” chemistry, strain-promoted azide-alkyne cycloaddition
ERLIC, electrostatic repulsion-hydrophilic interaction chromatography
MAX, mixed-mode strong anion exchange

Details

ISSN :
15359476
Volume :
20
Database :
OpenAIRE
Journal :
Molecular & Cellular Proteomics
Accession number :
edsair.doi.dedup.....ad350657f104086aa3b3bf8fb2be0f8c