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

      review-article
      1 , , 1 , 2 , 3 ,
      Molecular & Cellular Proteomics : MCP
      American Society for Biochemistry and Molecular Biology
      Glycosylation, glycopeptides, glycoproteomics, mass spectrometry, enrichment, chemical biology, affinity chromatography, lectins, hydrophilic interaction chromatography (HILIC), strong anion exchange electrostatic repulsion hydrophilic interaction chromatography (SAX-ERLIC) , AAL, Aleuria aurantia lectin, AX, anion exchange, ConA, concanavalin A, CuAAC, i.e., “click” chemistry, copper-catalyzed azide-alkyne cycloadditions, DIA, data-independent acquisition, ECD, electron capture dissociation, ERLIC, electrostatic repulsion-hydrophilic interaction chromatography, ETD, electron transfer dissociation, GalT1, β-1,4-galactosyltransferase 1, HCD, higher-energy collisional dissociation, HILIC, hydrophilic interaction chromatography, IMAC, immobilized metal affinity chromatography, IMS, ion mobility spectrometry, LAC, lectin affinity chromatography, M-LAC, multi-lectin affinity chromatography, M6P, mannose-6-phosphate, ManNAz, N-azidoacetylmannosamine, MAX, mixed-mode strong anion exchange, MOAC, metal oxide affinity chromatography, MS, mass spectrometry, Neu5Ac, N-acetylneuraminic acid, Neu5Gc, N-glycolylneuraminic acid, PGC, porous graphitic carbon, PTMs, post-translational modifications, RCA, ricinus communis agglutinin, SAX, strong anion exchange, Siglecs, sialic acid–binding immunoglobulin-type lectins, SPAAC, i.e., “copper-free click” chemistry, strain-promoted azide-alkyne cycloaddition, SPE, solid-phase extraction, WAX, weak anion exchange, WGA, wheat germ agglutinin, ZIC-HILIC, zwitterionic HILIC

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          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.

          Graphical Abstract

          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

          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.

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          Universal sample preparation method for proteome analysis.

          We describe a method, filter-aided sample preparation (FASP), which combines the advantages of in-gel and in-solution digestion for mass spectrometry-based proteomics. We completely solubilized the proteome in sodium dodecyl sulfate, which we then exchanged by urea on a standard filtration device. Peptides eluted after digestion on the filter were pure, allowing single-run analyses of organelles and an unprecedented depth of proteome coverage.
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            Glycosylation in health and disease

            The glycome describes the complete repertoire of glycoconjugates composed of carbohydrate chains, or glycans, that are covalently linked to lipid or protein molecules. Glycoconjugates are formed through a process called glycosylation and can differ in their glycan sequences, the connections between them and their length. Glycoconjugate synthesis is a dynamic process that depends on the local milieu of enzymes, sugar precursors and organelle structures as well as the cell types involved and cellular signals. Studies of rare genetic disorders that affect glycosylation first highlighted the biological importance of the glycome, and technological advances have improved our understanding of its heterogeneity and complexity. Researchers can now routinely assess how the secreted and cell-surface glycomes reflect overall cellular status in health and disease. In fact, changes in glycosylation can modulate inflammatory responses, enable viral immune escape, promote cancer cell metastasis or regulate apoptosis; the composition of the glycome also affects kidney function in health and disease. New insights into the structure and function of the glycome can now be applied to therapy development and could improve our ability to fine-tune immunological responses and inflammation, optimize the performance of therapeutic antibodies and boost immune responses to cancer. These examples illustrate the potential of the emerging field of 'glycomedicine'.
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              A stepwise huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes.

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                Author and article information

                Contributors
                Journal
                Mol Cell Proteomics
                Mol Cell Proteomics
                Molecular & Cellular Proteomics : MCP
                American Society for Biochemistry and Molecular Biology
                1535-9476
                1535-9484
                20 December 2020
                2021
                20 December 2020
                : 20
                : 100029
                Affiliations
                [1 ]Department of Chemistry, Stanford University, Stanford, California, USA
                [2 ]Howard Hughes Medical Institute, Stanford, California, USA
                [3 ]Department of Radiology, Canary Center at Stanford for Cancer Early Detection, Stanford University School of Medicine, Palo Alto, California, USA
                Author notes
                []For correspondence: Nicholas M. Riley; Sharon J. Pitteri. nmriley@ 123456stanford.edu spitteri@ 123456stanford.edu
                Article
                S1535-9476(20)35143-4 100029
                10.1074/mcp.R120.002277
                8724846
                33583771
                7ce8db6b-8902-4b1e-97ec-be93e972c115
                © 2020 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 4 August 2020
                : 14 September 2020
                Categories
                Review
                Special Issue: Glycoproteomics

                Molecular biology
                glycosylation,glycopeptides,glycoproteomics,mass spectrometry,enrichment,chemical biology,affinity chromatography,lectins,hydrophilic interaction chromatography (hilic),strong anion exchange electrostatic repulsion hydrophilic interaction chromatography (sax-erlic),aal, aleuria aurantia lectin,ax, anion exchange,cona, concanavalin a,cuaac, i.e., “click” chemistry, copper-catalyzed azide-alkyne cycloadditions,dia, data-independent acquisition,ecd, electron capture dissociation,erlic, electrostatic repulsion-hydrophilic interaction chromatography,etd, electron transfer dissociation,galt1, β-1,4-galactosyltransferase 1,hcd, higher-energy collisional dissociation,hilic, hydrophilic interaction chromatography,imac, immobilized metal affinity chromatography,ims, ion mobility spectrometry,lac, lectin affinity chromatography,m-lac, multi-lectin affinity chromatography,m6p, mannose-6-phosphate,mannaz, n-azidoacetylmannosamine,max, mixed-mode strong anion exchange,moac, metal oxide affinity chromatography,ms, mass spectrometry,neu5ac, n-acetylneuraminic acid,neu5gc, n-glycolylneuraminic acid,pgc, porous graphitic carbon,ptms, post-translational modifications,rca, ricinus communis agglutinin,sax, strong anion exchange,siglecs, sialic acid–binding immunoglobulin-type lectins,spaac, i.e., “copper-free click” chemistry, strain-promoted azide-alkyne cycloaddition,spe, solid-phase extraction,wax, weak anion exchange,wga, wheat germ agglutinin,zic-hilic, zwitterionic hilic
                Molecular biology
                glycosylation, glycopeptides, glycoproteomics, mass spectrometry, enrichment, chemical biology, affinity chromatography, lectins, hydrophilic interaction chromatography (hilic), strong anion exchange electrostatic repulsion hydrophilic interaction chromatography (sax-erlic), aal, aleuria aurantia lectin, ax, anion exchange, cona, concanavalin a, cuaac, i.e., “click” chemistry, copper-catalyzed azide-alkyne cycloadditions, dia, data-independent acquisition, ecd, electron capture dissociation, erlic, electrostatic repulsion-hydrophilic interaction chromatography, etd, electron transfer dissociation, galt1, β-1,4-galactosyltransferase 1, hcd, higher-energy collisional dissociation, hilic, hydrophilic interaction chromatography, imac, immobilized metal affinity chromatography, ims, ion mobility spectrometry, lac, lectin affinity chromatography, m-lac, multi-lectin affinity chromatography, m6p, mannose-6-phosphate, mannaz, n-azidoacetylmannosamine, max, mixed-mode strong anion exchange, moac, metal oxide affinity chromatography, ms, mass spectrometry, neu5ac, n-acetylneuraminic acid, neu5gc, n-glycolylneuraminic acid, pgc, porous graphitic carbon, ptms, post-translational modifications, rca, ricinus communis agglutinin, sax, strong anion exchange, siglecs, sialic acid–binding immunoglobulin-type lectins, spaac, i.e., “copper-free click” chemistry, strain-promoted azide-alkyne cycloaddition, spe, solid-phase extraction, wax, weak anion exchange, wga, wheat germ agglutinin, zic-hilic, zwitterionic hilic

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