Quantitative NMR for the structural analysis of novel bivalent glycoconjugates as vaccine candidates

Novel unimolecular bivalent glycoconjugates were assembled combining several functionalized capsular polysaccharides of Streptococcus pneumoniae and Neisseria meningitidis to a carrier protein by using an effective strategy based on the Ugi 4-component reaction. The development of multivalent glycoc...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of pharmaceutical and biomedical analysis 2022-05, Vol.214, p.114721-114721, Article 114721
Hauptverfasser: Humpierre, Ana R., Zanuy, Abel, Saenz, Mirelys, Vasco, Aldrin V., Méndez, Yanira, Westermann, Bernhard, Cardoso, Félix, Quintero, Lauren, Santana, Darielys, Verez, Vicente, Valdés, Yury, Rivera, Daniel G., Garrido, Raine
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 114721
container_issue
container_start_page 114721
container_title Journal of pharmaceutical and biomedical analysis
container_volume 214
creator Humpierre, Ana R.
Zanuy, Abel
Saenz, Mirelys
Vasco, Aldrin V.
Méndez, Yanira
Westermann, Bernhard
Cardoso, Félix
Quintero, Lauren
Santana, Darielys
Verez, Vicente
Valdés, Yury
Rivera, Daniel G.
Garrido, Raine
description Novel unimolecular bivalent glycoconjugates were assembled combining several functionalized capsular polysaccharides of Streptococcus pneumoniae and Neisseria meningitidis to a carrier protein by using an effective strategy based on the Ugi 4-component reaction. The development of multivalent glycoconjugates opens new opportunities in the field of vaccine design, but their high structural complexity involves new analytical challenges. Nuclear Magnetic Resonance has found wide applications in the characterization and impurity profiling of carbohydrate-based vaccines. Eight bivalent conjugates were studied by quantitative NMR analyzing the structural identity, the content of each capsular polysaccharide, the ratios between polysaccharides, the polysaccharide to protein ratios and undesirable contaminants. The qNMR technique involves experiments with several modified parameters for obtaining spectra with quantifiable signals. In addition, the achieved NMR results were combined with the results of colorimetric assay and Size Exclusion HPLC for assessing the protein content and free protein percentage, respectively. The application of quantitative NMR showed to be efficient to clear up the new structural complexities while allowing the quantitative assessment of the components. •Conjugates were built by assembling two capsular polysaccharides to a protein.•Quantitative NMR spectra confirmed the structural complexity of the conjugates.•Quantitative NMR can be used for ensuring the quality of these novel conjugates.
doi_str_mv 10.1016/j.jpba.2022.114721
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2644019770</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S073170852200142X</els_id><sourcerecordid>2644019770</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-d21930a36c8408d35bce8356a085b3a3c5ae5c808812612f289dfabde46c4b7b3</originalsourceid><addsrcrecordid>eNp9kE2LFDEQhoMo7rj6BzxIjl56zEd_pMGLLH7BqigK3kJ1pXpN05OMSbph_r09zOrRU0HV875QD2PPpdhLIdtX0346DrBXQqm9lHWn5AO2k6bTlWrrnw_ZTnRaVp0wzRV7kvMkhGhkXz9mV7rR2vR1s2Pu6wKh-ALFr8Q_f_rGx5h4-UU8l7RgWRLMHALMp-wzjyMPcaWZD36FmULhd_MJI8YwLXdQKHPIfAVEH4gjBOfdefuUPRphzvTsfl6zH-_efr_5UN1-ef_x5s1thbppS-WU7LUA3aKphXG6GZDMdoHtg0GDxgaoQSOMkaqValSmdyMMjuoW66Eb9DV7eek9pvh7oVzswWekeYZAccl201IL2Xed2FB1QTHFnBON9pj8AdLJSmHPdu1kz3bt2a692N1CL-77l-FA7l_kr84NeH0BaPty9ZRsRk8ByflEWKyL_n_9fwDm_4yD</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2644019770</pqid></control><display><type>article</type><title>Quantitative NMR for the structural analysis of novel bivalent glycoconjugates as vaccine candidates</title><source>Elsevier ScienceDirect Journals</source><creator>Humpierre, Ana R. ; Zanuy, Abel ; Saenz, Mirelys ; Vasco, Aldrin V. ; Méndez, Yanira ; Westermann, Bernhard ; Cardoso, Félix ; Quintero, Lauren ; Santana, Darielys ; Verez, Vicente ; Valdés, Yury ; Rivera, Daniel G. ; Garrido, Raine</creator><creatorcontrib>Humpierre, Ana R. ; Zanuy, Abel ; Saenz, Mirelys ; Vasco, Aldrin V. ; Méndez, Yanira ; Westermann, Bernhard ; Cardoso, Félix ; Quintero, Lauren ; Santana, Darielys ; Verez, Vicente ; Valdés, Yury ; Rivera, Daniel G. ; Garrido, Raine</creatorcontrib><description>Novel unimolecular bivalent glycoconjugates were assembled combining several functionalized capsular polysaccharides of Streptococcus pneumoniae and Neisseria meningitidis to a carrier protein by using an effective strategy based on the Ugi 4-component reaction. The development of multivalent glycoconjugates opens new opportunities in the field of vaccine design, but their high structural complexity involves new analytical challenges. Nuclear Magnetic Resonance has found wide applications in the characterization and impurity profiling of carbohydrate-based vaccines. Eight bivalent conjugates were studied by quantitative NMR analyzing the structural identity, the content of each capsular polysaccharide, the ratios between polysaccharides, the polysaccharide to protein ratios and undesirable contaminants. The qNMR technique involves experiments with several modified parameters for obtaining spectra with quantifiable signals. In addition, the achieved NMR results were combined with the results of colorimetric assay and Size Exclusion HPLC for assessing the protein content and free protein percentage, respectively. The application of quantitative NMR showed to be efficient to clear up the new structural complexities while allowing the quantitative assessment of the components. •Conjugates were built by assembling two capsular polysaccharides to a protein.•Quantitative NMR spectra confirmed the structural complexity of the conjugates.•Quantitative NMR can be used for ensuring the quality of these novel conjugates.</description><identifier>ISSN: 0731-7085</identifier><identifier>EISSN: 1873-264X</identifier><identifier>DOI: 10.1016/j.jpba.2022.114721</identifier><identifier>PMID: 35338945</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Analysis ; Conjugates ; Multicomponent chemistry ; QNMR ; Vaccines</subject><ispartof>Journal of pharmaceutical and biomedical analysis, 2022-05, Vol.214, p.114721-114721, Article 114721</ispartof><rights>2022 Elsevier B.V.</rights><rights>Copyright © 2022 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-d21930a36c8408d35bce8356a085b3a3c5ae5c808812612f289dfabde46c4b7b3</citedby><cites>FETCH-LOGICAL-c356t-d21930a36c8408d35bce8356a085b3a3c5ae5c808812612f289dfabde46c4b7b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpba.2022.114721$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35338945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Humpierre, Ana R.</creatorcontrib><creatorcontrib>Zanuy, Abel</creatorcontrib><creatorcontrib>Saenz, Mirelys</creatorcontrib><creatorcontrib>Vasco, Aldrin V.</creatorcontrib><creatorcontrib>Méndez, Yanira</creatorcontrib><creatorcontrib>Westermann, Bernhard</creatorcontrib><creatorcontrib>Cardoso, Félix</creatorcontrib><creatorcontrib>Quintero, Lauren</creatorcontrib><creatorcontrib>Santana, Darielys</creatorcontrib><creatorcontrib>Verez, Vicente</creatorcontrib><creatorcontrib>Valdés, Yury</creatorcontrib><creatorcontrib>Rivera, Daniel G.</creatorcontrib><creatorcontrib>Garrido, Raine</creatorcontrib><title>Quantitative NMR for the structural analysis of novel bivalent glycoconjugates as vaccine candidates</title><title>Journal of pharmaceutical and biomedical analysis</title><addtitle>J Pharm Biomed Anal</addtitle><description>Novel unimolecular bivalent glycoconjugates were assembled combining several functionalized capsular polysaccharides of Streptococcus pneumoniae and Neisseria meningitidis to a carrier protein by using an effective strategy based on the Ugi 4-component reaction. The development of multivalent glycoconjugates opens new opportunities in the field of vaccine design, but their high structural complexity involves new analytical challenges. Nuclear Magnetic Resonance has found wide applications in the characterization and impurity profiling of carbohydrate-based vaccines. Eight bivalent conjugates were studied by quantitative NMR analyzing the structural identity, the content of each capsular polysaccharide, the ratios between polysaccharides, the polysaccharide to protein ratios and undesirable contaminants. The qNMR technique involves experiments with several modified parameters for obtaining spectra with quantifiable signals. In addition, the achieved NMR results were combined with the results of colorimetric assay and Size Exclusion HPLC for assessing the protein content and free protein percentage, respectively. The application of quantitative NMR showed to be efficient to clear up the new structural complexities while allowing the quantitative assessment of the components. •Conjugates were built by assembling two capsular polysaccharides to a protein.•Quantitative NMR spectra confirmed the structural complexity of the conjugates.•Quantitative NMR can be used for ensuring the quality of these novel conjugates.</description><subject>Analysis</subject><subject>Conjugates</subject><subject>Multicomponent chemistry</subject><subject>QNMR</subject><subject>Vaccines</subject><issn>0731-7085</issn><issn>1873-264X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp9kE2LFDEQhoMo7rj6BzxIjl56zEd_pMGLLH7BqigK3kJ1pXpN05OMSbph_r09zOrRU0HV875QD2PPpdhLIdtX0346DrBXQqm9lHWn5AO2k6bTlWrrnw_ZTnRaVp0wzRV7kvMkhGhkXz9mV7rR2vR1s2Pu6wKh-ALFr8Q_f_rGx5h4-UU8l7RgWRLMHALMp-wzjyMPcaWZD36FmULhd_MJI8YwLXdQKHPIfAVEH4gjBOfdefuUPRphzvTsfl6zH-_efr_5UN1-ef_x5s1thbppS-WU7LUA3aKphXG6GZDMdoHtg0GDxgaoQSOMkaqValSmdyMMjuoW66Eb9DV7eek9pvh7oVzswWekeYZAccl201IL2Xed2FB1QTHFnBON9pj8AdLJSmHPdu1kz3bt2a692N1CL-77l-FA7l_kr84NeH0BaPty9ZRsRk8ByflEWKyL_n_9fwDm_4yD</recordid><startdate>20220530</startdate><enddate>20220530</enddate><creator>Humpierre, Ana R.</creator><creator>Zanuy, Abel</creator><creator>Saenz, Mirelys</creator><creator>Vasco, Aldrin V.</creator><creator>Méndez, Yanira</creator><creator>Westermann, Bernhard</creator><creator>Cardoso, Félix</creator><creator>Quintero, Lauren</creator><creator>Santana, Darielys</creator><creator>Verez, Vicente</creator><creator>Valdés, Yury</creator><creator>Rivera, Daniel G.</creator><creator>Garrido, Raine</creator><general>Elsevier B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20220530</creationdate><title>Quantitative NMR for the structural analysis of novel bivalent glycoconjugates as vaccine candidates</title><author>Humpierre, Ana R. ; Zanuy, Abel ; Saenz, Mirelys ; Vasco, Aldrin V. ; Méndez, Yanira ; Westermann, Bernhard ; Cardoso, Félix ; Quintero, Lauren ; Santana, Darielys ; Verez, Vicente ; Valdés, Yury ; Rivera, Daniel G. ; Garrido, Raine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-d21930a36c8408d35bce8356a085b3a3c5ae5c808812612f289dfabde46c4b7b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Conjugates</topic><topic>Multicomponent chemistry</topic><topic>QNMR</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Humpierre, Ana R.</creatorcontrib><creatorcontrib>Zanuy, Abel</creatorcontrib><creatorcontrib>Saenz, Mirelys</creatorcontrib><creatorcontrib>Vasco, Aldrin V.</creatorcontrib><creatorcontrib>Méndez, Yanira</creatorcontrib><creatorcontrib>Westermann, Bernhard</creatorcontrib><creatorcontrib>Cardoso, Félix</creatorcontrib><creatorcontrib>Quintero, Lauren</creatorcontrib><creatorcontrib>Santana, Darielys</creatorcontrib><creatorcontrib>Verez, Vicente</creatorcontrib><creatorcontrib>Valdés, Yury</creatorcontrib><creatorcontrib>Rivera, Daniel G.</creatorcontrib><creatorcontrib>Garrido, Raine</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Humpierre, Ana R.</au><au>Zanuy, Abel</au><au>Saenz, Mirelys</au><au>Vasco, Aldrin V.</au><au>Méndez, Yanira</au><au>Westermann, Bernhard</au><au>Cardoso, Félix</au><au>Quintero, Lauren</au><au>Santana, Darielys</au><au>Verez, Vicente</au><au>Valdés, Yury</au><au>Rivera, Daniel G.</au><au>Garrido, Raine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantitative NMR for the structural analysis of novel bivalent glycoconjugates as vaccine candidates</atitle><jtitle>Journal of pharmaceutical and biomedical analysis</jtitle><addtitle>J Pharm Biomed Anal</addtitle><date>2022-05-30</date><risdate>2022</risdate><volume>214</volume><spage>114721</spage><epage>114721</epage><pages>114721-114721</pages><artnum>114721</artnum><issn>0731-7085</issn><eissn>1873-264X</eissn><abstract>Novel unimolecular bivalent glycoconjugates were assembled combining several functionalized capsular polysaccharides of Streptococcus pneumoniae and Neisseria meningitidis to a carrier protein by using an effective strategy based on the Ugi 4-component reaction. The development of multivalent glycoconjugates opens new opportunities in the field of vaccine design, but their high structural complexity involves new analytical challenges. Nuclear Magnetic Resonance has found wide applications in the characterization and impurity profiling of carbohydrate-based vaccines. Eight bivalent conjugates were studied by quantitative NMR analyzing the structural identity, the content of each capsular polysaccharide, the ratios between polysaccharides, the polysaccharide to protein ratios and undesirable contaminants. The qNMR technique involves experiments with several modified parameters for obtaining spectra with quantifiable signals. In addition, the achieved NMR results were combined with the results of colorimetric assay and Size Exclusion HPLC for assessing the protein content and free protein percentage, respectively. The application of quantitative NMR showed to be efficient to clear up the new structural complexities while allowing the quantitative assessment of the components. •Conjugates were built by assembling two capsular polysaccharides to a protein.•Quantitative NMR spectra confirmed the structural complexity of the conjugates.•Quantitative NMR can be used for ensuring the quality of these novel conjugates.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>35338945</pmid><doi>10.1016/j.jpba.2022.114721</doi><tpages>1</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0731-7085
ispartof Journal of pharmaceutical and biomedical analysis, 2022-05, Vol.214, p.114721-114721, Article 114721
issn 0731-7085
1873-264X
language eng
recordid cdi_proquest_miscellaneous_2644019770
source Elsevier ScienceDirect Journals
subjects Analysis
Conjugates
Multicomponent chemistry
QNMR
Vaccines
title Quantitative NMR for the structural analysis of novel bivalent glycoconjugates as vaccine candidates
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T03%3A04%3A01IST&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=Quantitative%20NMR%20for%20the%20structural%20analysis%20of%20novel%20bivalent%20glycoconjugates%20as%20vaccine%20candidates&rft.jtitle=Journal%20of%20pharmaceutical%20and%20biomedical%20analysis&rft.au=Humpierre,%20Ana%20R.&rft.date=2022-05-30&rft.volume=214&rft.spage=114721&rft.epage=114721&rft.pages=114721-114721&rft.artnum=114721&rft.issn=0731-7085&rft.eissn=1873-264X&rft_id=info:doi/10.1016/j.jpba.2022.114721&rft_dat=%3Cproquest_cross%3E2644019770%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=2644019770&rft_id=info:pmid/35338945&rft_els_id=S073170852200142X&rfr_iscdi=true