Development of electrophoretic conditions for the characterization of protein glycoforms by capillary electrophoresis—electrospray mass spectrometry

A capillary electrophoresis (CE) method using acidic buffers and capillaries coated with Polybrene, a cationic polymer has been developed for the separation of glycoproteins and glycopeptides. Electrophoretic conditions have been optimized to provide resolution of individual glycoforms observed for...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of Chromatography A 1996-01, Vol.720 (1), p.409-427
Hauptverfasser: Kelly, J.F, Locke, S.J, Ramaley, L, Thibault, P
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 427
container_issue 1
container_start_page 409
container_title Journal of Chromatography A
container_volume 720
creator Kelly, J.F
Locke, S.J
Ramaley, L
Thibault, P
description A capillary electrophoresis (CE) method using acidic buffers and capillaries coated with Polybrene, a cationic polymer has been developed for the separation of glycoproteins and glycopeptides. Electrophoretic conditions have been optimized to provide resolution of individual glycoforms observed for different glycoprotein preparations. These conditions were found to be entirely compatible with the operation of electrospray mass spectrometry (ESMS), which facilitated the assignments of possible carbohydrate compositions of glycopeptides arising from digests of glycoproteins. By using operating conditions enhancing the formation of oxonium fragment ions prior to mass spectral analysis, selective identification of glycopeptides was achieved for complex samples such as those from proteolytic digests or chemical cleavages. Examples of applications are presented for ribonuclease B, ovalbumin, horseradish peroxidase, and a lectin from Erithrina corallodendron using both CE-ESMS and CE with ultraviolet detection (CE-UV).
doi_str_mv 10.1016/0021-9673(94)01197-4
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_77972389</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0021967394011974</els_id><sourcerecordid>77972389</sourcerecordid><originalsourceid>FETCH-LOGICAL-c423t-ffd6c9a75de68a4b5e8d9ac41ac3d9d6a6966a4d3547aafa778581cbc6609d2f3</originalsourceid><addsrcrecordid>eNp9UU1P3DAU9IEKKPQftJJPqBxS7MRrxxekCuiHhMSlPVve55euqyRObS9SeuqPqPiB_SV12BUSF06WZuaN38wj5C1nHzjj8oKxmldaqua9FueMc60qcUCOn-Aj8jqln4xxxVR9SA5byXjNxDF5uMZ77MM04Jhp6Cj2CDmGaRMiZg8Uwuh89mFMtAuR5g1S2NhoIWP0v-3CLGNTDBn9SH_0M4QiHBJdzxTs5PvexvmZbfLp35-_eyRN0c50sCnRND0iA-Y4n5JXne0Tvtm_J-T7p5tvV1-q27vPX68-3lYg6iZXXeckaKtWDmVrxXqFrdMWBLfQOO2klVpKK1yzEsrazirVrloOa5CSaVd3zQk52_mWAL-2mLIZfAIsS48YtskopVXdtLoIxU4IZecUsTNT9EOJZjgzywnM0rVZujZamMcTGFHG3u39t-sB3dPQvv_CX-54LCHvPUaTwOMI6HwsbRgX_Msf_AfE559c</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>77972389</pqid></control><display><type>article</type><title>Development of electrophoretic conditions for the characterization of protein glycoforms by capillary electrophoresis—electrospray mass spectrometry</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Kelly, J.F ; Locke, S.J ; Ramaley, L ; Thibault, P</creator><creatorcontrib>Kelly, J.F ; Locke, S.J ; Ramaley, L ; Thibault, P</creatorcontrib><description>A capillary electrophoresis (CE) method using acidic buffers and capillaries coated with Polybrene, a cationic polymer has been developed for the separation of glycoproteins and glycopeptides. Electrophoretic conditions have been optimized to provide resolution of individual glycoforms observed for different glycoprotein preparations. These conditions were found to be entirely compatible with the operation of electrospray mass spectrometry (ESMS), which facilitated the assignments of possible carbohydrate compositions of glycopeptides arising from digests of glycoproteins. By using operating conditions enhancing the formation of oxonium fragment ions prior to mass spectral analysis, selective identification of glycopeptides was achieved for complex samples such as those from proteolytic digests or chemical cleavages. Examples of applications are presented for ribonuclease B, ovalbumin, horseradish peroxidase, and a lectin from Erithrina corallodendron using both CE-ESMS and CE with ultraviolet detection (CE-UV).</description><identifier>ISSN: 0021-9673</identifier><identifier>DOI: 10.1016/0021-9673(94)01197-4</identifier><identifier>PMID: 8601204</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Carbohydrate Conformation ; Carbohydrate Sequence ; Electrophoresis, Capillary - methods ; Glycoproteins - analysis ; Hydrolysis ; Mass Spectrometry - methods ; Molecular Sequence Data ; Ovalbumin - analysis ; Ribonucleases - analysis ; Spectrophotometry, Ultraviolet</subject><ispartof>Journal of Chromatography A, 1996-01, Vol.720 (1), p.409-427</ispartof><rights>1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-ffd6c9a75de68a4b5e8d9ac41ac3d9d6a6966a4d3547aafa778581cbc6609d2f3</citedby><cites>FETCH-LOGICAL-c423t-ffd6c9a75de68a4b5e8d9ac41ac3d9d6a6966a4d3547aafa778581cbc6609d2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0021-9673(94)01197-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8601204$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kelly, J.F</creatorcontrib><creatorcontrib>Locke, S.J</creatorcontrib><creatorcontrib>Ramaley, L</creatorcontrib><creatorcontrib>Thibault, P</creatorcontrib><title>Development of electrophoretic conditions for the characterization of protein glycoforms by capillary electrophoresis—electrospray mass spectrometry</title><title>Journal of Chromatography A</title><addtitle>J Chromatogr A</addtitle><description>A capillary electrophoresis (CE) method using acidic buffers and capillaries coated with Polybrene, a cationic polymer has been developed for the separation of glycoproteins and glycopeptides. Electrophoretic conditions have been optimized to provide resolution of individual glycoforms observed for different glycoprotein preparations. These conditions were found to be entirely compatible with the operation of electrospray mass spectrometry (ESMS), which facilitated the assignments of possible carbohydrate compositions of glycopeptides arising from digests of glycoproteins. By using operating conditions enhancing the formation of oxonium fragment ions prior to mass spectral analysis, selective identification of glycopeptides was achieved for complex samples such as those from proteolytic digests or chemical cleavages. Examples of applications are presented for ribonuclease B, ovalbumin, horseradish peroxidase, and a lectin from Erithrina corallodendron using both CE-ESMS and CE with ultraviolet detection (CE-UV).</description><subject>Carbohydrate Conformation</subject><subject>Carbohydrate Sequence</subject><subject>Electrophoresis, Capillary - methods</subject><subject>Glycoproteins - analysis</subject><subject>Hydrolysis</subject><subject>Mass Spectrometry - methods</subject><subject>Molecular Sequence Data</subject><subject>Ovalbumin - analysis</subject><subject>Ribonucleases - analysis</subject><subject>Spectrophotometry, Ultraviolet</subject><issn>0021-9673</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UU1P3DAU9IEKKPQftJJPqBxS7MRrxxekCuiHhMSlPVve55euqyRObS9SeuqPqPiB_SV12BUSF06WZuaN38wj5C1nHzjj8oKxmldaqua9FueMc60qcUCOn-Aj8jqln4xxxVR9SA5byXjNxDF5uMZ77MM04Jhp6Cj2CDmGaRMiZg8Uwuh89mFMtAuR5g1S2NhoIWP0v-3CLGNTDBn9SH_0M4QiHBJdzxTs5PvexvmZbfLp35-_eyRN0c50sCnRND0iA-Y4n5JXne0Tvtm_J-T7p5tvV1-q27vPX68-3lYg6iZXXeckaKtWDmVrxXqFrdMWBLfQOO2klVpKK1yzEsrazirVrloOa5CSaVd3zQk52_mWAL-2mLIZfAIsS48YtskopVXdtLoIxU4IZecUsTNT9EOJZjgzywnM0rVZujZamMcTGFHG3u39t-sB3dPQvv_CX-54LCHvPUaTwOMI6HwsbRgX_Msf_AfE559c</recordid><startdate>19960112</startdate><enddate>19960112</enddate><creator>Kelly, J.F</creator><creator>Locke, S.J</creator><creator>Ramaley, L</creator><creator>Thibault, P</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>19960112</creationdate><title>Development of electrophoretic conditions for the characterization of protein glycoforms by capillary electrophoresis—electrospray mass spectrometry</title><author>Kelly, J.F ; Locke, S.J ; Ramaley, L ; Thibault, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-ffd6c9a75de68a4b5e8d9ac41ac3d9d6a6966a4d3547aafa778581cbc6609d2f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Carbohydrate Conformation</topic><topic>Carbohydrate Sequence</topic><topic>Electrophoresis, Capillary - methods</topic><topic>Glycoproteins - analysis</topic><topic>Hydrolysis</topic><topic>Mass Spectrometry - methods</topic><topic>Molecular Sequence Data</topic><topic>Ovalbumin - analysis</topic><topic>Ribonucleases - analysis</topic><topic>Spectrophotometry, Ultraviolet</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kelly, J.F</creatorcontrib><creatorcontrib>Locke, S.J</creatorcontrib><creatorcontrib>Ramaley, L</creatorcontrib><creatorcontrib>Thibault, P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of Chromatography A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kelly, J.F</au><au>Locke, S.J</au><au>Ramaley, L</au><au>Thibault, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of electrophoretic conditions for the characterization of protein glycoforms by capillary electrophoresis—electrospray mass spectrometry</atitle><jtitle>Journal of Chromatography A</jtitle><addtitle>J Chromatogr A</addtitle><date>1996-01-12</date><risdate>1996</risdate><volume>720</volume><issue>1</issue><spage>409</spage><epage>427</epage><pages>409-427</pages><issn>0021-9673</issn><abstract>A capillary electrophoresis (CE) method using acidic buffers and capillaries coated with Polybrene, a cationic polymer has been developed for the separation of glycoproteins and glycopeptides. Electrophoretic conditions have been optimized to provide resolution of individual glycoforms observed for different glycoprotein preparations. These conditions were found to be entirely compatible with the operation of electrospray mass spectrometry (ESMS), which facilitated the assignments of possible carbohydrate compositions of glycopeptides arising from digests of glycoproteins. By using operating conditions enhancing the formation of oxonium fragment ions prior to mass spectral analysis, selective identification of glycopeptides was achieved for complex samples such as those from proteolytic digests or chemical cleavages. Examples of applications are presented for ribonuclease B, ovalbumin, horseradish peroxidase, and a lectin from Erithrina corallodendron using both CE-ESMS and CE with ultraviolet detection (CE-UV).</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>8601204</pmid><doi>10.1016/0021-9673(94)01197-4</doi><tpages>19</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9673
ispartof Journal of Chromatography A, 1996-01, Vol.720 (1), p.409-427
issn 0021-9673
language eng
recordid cdi_proquest_miscellaneous_77972389
source MEDLINE; Access via ScienceDirect (Elsevier)
subjects Carbohydrate Conformation
Carbohydrate Sequence
Electrophoresis, Capillary - methods
Glycoproteins - analysis
Hydrolysis
Mass Spectrometry - methods
Molecular Sequence Data
Ovalbumin - analysis
Ribonucleases - analysis
Spectrophotometry, Ultraviolet
title Development of electrophoretic conditions for the characterization of protein glycoforms by capillary electrophoresis—electrospray mass spectrometry
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T01%3A18%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Development%20of%20electrophoretic%20conditions%20for%20the%20characterization%20of%20protein%20glycoforms%20by%20capillary%20electrophoresis%E2%80%94electrospray%20mass%20spectrometry&rft.jtitle=Journal%20of%20Chromatography%20A&rft.au=Kelly,%20J.F&rft.date=1996-01-12&rft.volume=720&rft.issue=1&rft.spage=409&rft.epage=427&rft.pages=409-427&rft.issn=0021-9673&rft_id=info:doi/10.1016/0021-9673(94)01197-4&rft_dat=%3Cproquest_cross%3E77972389%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=77972389&rft_id=info:pmid/8601204&rft_els_id=0021967394011974&rfr_iscdi=true