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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 |
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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. 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.</description><identifier>ISSN: 1615-9306</identifier><identifier>EISSN: 1615-9314</identifier><identifier>DOI: 10.1002/jssc.201900983</identifier><identifier>PMID: 31970866</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>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</subject><ispartof>Journal of separation science, 2020-04, Vol.43 (7), p.1348-1355</ispartof><rights>2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4716-3305ba2c96272e5d43b81b951e2b2676141ee8ae8f99475685e3c8c3d83bdb33</citedby><cites>FETCH-LOGICAL-c4716-3305ba2c96272e5d43b81b951e2b2676141ee8ae8f99475685e3c8c3d83bdb33</cites><orcidid>0000-0002-2090-5072</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31970866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sajid, Muhammad Salman</creatorcontrib><creatorcontrib>Jabeen, Fahmida</creatorcontrib><creatorcontrib>Hussain, Dilshad</creatorcontrib><creatorcontrib>Gardner, Qurra‐tul‐Ann Afza</creatorcontrib><creatorcontrib>Ashiq, Muhammad Naeem</creatorcontrib><creatorcontrib>Najam‐ul‐Haq, Muhammad</creatorcontrib><title>Boronic acid functionalized fibrous cellulose for the selective enrichment of glycopeptides</title><title>Journal of separation science</title><addtitle>J Sep Sci</addtitle><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.</description><subject>Acids</subject><subject>Adsorption</subject><subject>Animals</subject><subject>Antibiotics</subject><subject>boronic acid</subject><subject>Boronic Acids - blood</subject><subject>Boronic Acids - chemistry</subject><subject>Boronic Acids - metabolism</subject><subject>Cattle</subject><subject>Cellulose</subject><subject>Cellulose - blood</subject><subject>Cellulose - chemistry</subject><subject>Cellulose - metabolism</subject><subject>Cellulose fibers</subject><subject>Enrichment</subject><subject>Fourier transforms</subject><subject>Glycopeptides</subject><subject>Glycopeptides - blood</subject><subject>Glycopeptides - chemistry</subject><subject>Glycopeptides - metabolism</subject><subject>glycopeptides enrichment</subject><subject>Glycoproteins</subject><subject>Horseradish Peroxidase - metabolism</subject><subject>human serum</subject><subject>Humans</subject><subject>Immunoglobulins - metabolism</subject><subject>mass spectrometry</subject><subject>Morphology</subject><subject>Peroxidase</subject><subject>Polysaccharides</subject><subject>Proteins</subject><subject>Serum albumin</subject><subject>Serum Albumin, Bovine - metabolism</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><issn>1615-9306</issn><issn>1615-9314</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqF0DtPwzAUBWALgSgUVkZkiYUlxY_EsUeoeKoSQ7sxRIlzQ105cbETUPn1JGrpwMJkW_p8dO9B6IKSCSWE3axC0BNGqCJESX6ATqigSaQ4jQ_3dyJG6DSEFSE0lYocoxGnKiVSiBP0due8a4zGuTYlrrpGt8Y1uTXf0D9N4V0XsAZrO-sC4Mp53C4BB7DQy0_A0HijlzU0LXYVfrcb7dawbk0J4QwdVbkNcL47x2jxcL-YPkWz18fn6e0s0nFKRcQ5SYqcaSVYyiApY15IWqiEAiuYSAWNKYDMQVZKxWkiZAJcS81LyYuy4HyMrrexa-8-OghtVpswjJw30E-fMR7HjEkmRU-v_tCV63y_7qCkopwJKns12SrtXQgeqmztTZ37TUZJNrSeDa1n-9b7D5e72K6oodzz35p7EG_Bl7Gw-Scue5nPpyLlgv8AqCiN-g</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Sajid, Muhammad Salman</creator><creator>Jabeen, Fahmida</creator><creator>Hussain, Dilshad</creator><creator>Gardner, Qurra‐tul‐Ann Afza</creator><creator>Ashiq, Muhammad Naeem</creator><creator>Najam‐ul‐Haq, Muhammad</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2090-5072</orcidid></search><sort><creationdate>202004</creationdate><title>Boronic acid functionalized fibrous cellulose for the selective enrichment of glycopeptides</title><author>Sajid, Muhammad Salman ; Jabeen, Fahmida ; Hussain, Dilshad ; Gardner, Qurra‐tul‐Ann Afza ; Ashiq, Muhammad Naeem ; Najam‐ul‐Haq, Muhammad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4716-3305ba2c96272e5d43b81b951e2b2676141ee8ae8f99475685e3c8c3d83bdb33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acids</topic><topic>Adsorption</topic><topic>Animals</topic><topic>Antibiotics</topic><topic>boronic acid</topic><topic>Boronic Acids - blood</topic><topic>Boronic Acids - chemistry</topic><topic>Boronic Acids - metabolism</topic><topic>Cattle</topic><topic>Cellulose</topic><topic>Cellulose - blood</topic><topic>Cellulose - chemistry</topic><topic>Cellulose - metabolism</topic><topic>Cellulose fibers</topic><topic>Enrichment</topic><topic>Fourier transforms</topic><topic>Glycopeptides</topic><topic>Glycopeptides - blood</topic><topic>Glycopeptides - chemistry</topic><topic>Glycopeptides - metabolism</topic><topic>glycopeptides enrichment</topic><topic>Glycoproteins</topic><topic>Horseradish Peroxidase - metabolism</topic><topic>human serum</topic><topic>Humans</topic><topic>Immunoglobulins - metabolism</topic><topic>mass spectrometry</topic><topic>Morphology</topic><topic>Peroxidase</topic><topic>Polysaccharides</topic><topic>Proteins</topic><topic>Serum albumin</topic><topic>Serum Albumin, Bovine - metabolism</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sajid, Muhammad Salman</creatorcontrib><creatorcontrib>Jabeen, Fahmida</creatorcontrib><creatorcontrib>Hussain, Dilshad</creatorcontrib><creatorcontrib>Gardner, Qurra‐tul‐Ann Afza</creatorcontrib><creatorcontrib>Ashiq, Muhammad Naeem</creatorcontrib><creatorcontrib>Najam‐ul‐Haq, Muhammad</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of separation science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sajid, Muhammad Salman</au><au>Jabeen, Fahmida</au><au>Hussain, Dilshad</au><au>Gardner, Qurra‐tul‐Ann Afza</au><au>Ashiq, Muhammad Naeem</au><au>Najam‐ul‐Haq, Muhammad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Boronic acid functionalized fibrous cellulose for the selective enrichment of glycopeptides</atitle><jtitle>Journal of separation science</jtitle><addtitle>J Sep Sci</addtitle><date>2020-04</date><risdate>2020</risdate><volume>43</volume><issue>7</issue><spage>1348</spage><epage>1355</epage><pages>1348-1355</pages><issn>1615-9306</issn><eissn>1615-9314</eissn><abstract>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.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31970866</pmid><doi>10.1002/jssc.201900983</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2090-5072</orcidid></addata></record> |
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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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