ESI-MS reveals preferential complex formation of carbohydrates with -sinapinic acid compared with the -isomer

Cinnamic acid derivatives including 3,5-dimethoxy-4-hydroxycinnamic acid, also referred to as sinapinic acid (SA), are efficient matrices used in matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). Previous findings have shown that Z -sinapinic acid (ZSA) outperforms E -cinnami...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:New journal of chemistry 2022-10, Vol.46 (38), p.18563-18574
Hauptverfasser: De León, Tobías Schmidt, Salum, María Laura, Matsushita, Yasuyuki, Fukushima, Kazuhiko, Monge, María Eugenia, Erra-Balsells, Rosa
Format: Artikel
Sprache:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 18574
container_issue 38
container_start_page 18563
container_title New journal of chemistry
container_volume 46
creator De León, Tobías Schmidt
Salum, María Laura
Matsushita, Yasuyuki
Fukushima, Kazuhiko
Monge, María Eugenia
Erra-Balsells, Rosa
description Cinnamic acid derivatives including 3,5-dimethoxy-4-hydroxycinnamic acid, also referred to as sinapinic acid (SA), are efficient matrices used in matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). Previous findings have shown that Z -sinapinic acid (ZSA) outperforms E -cinnamic acids for carbohydrate (Carb) analysis, probably due to geometry-induced changes in analyte-matrix interactions at the molecular level, prompted by the cinnamic alkene rigid bond. In the present work, direct infusion electrospray ionization mass spectrometry (DI-ESI-MS) experiments were conducted to investigate the behavior of these acids as ligands for neutral Carb non-covalent complex formation. The ionization efficiency and binding affinities of these small molecules were evaluated towards seven Carbs with different monosaccharide composition and length. Experimental results were interpreted with the assistance of computational calculations. ESA, with higher calculated volume and lower acidity than ZSA, exhibited an experimental ESI efficiency similar to the latter. However, titration experiments showed that the [Acid + Carb] gas complex is preferentially formed with ZSA than ESA when both ligands are present in solution. Results from CID experiments support the formation of more stable complexes between larger Carbs and the ZSA isomer compared to the E -form. The change of molecule volume and polarity in the synthesized isotopically labeled ESA, E -3,5-di(methoxy-d3)-4-hydroxycinnamic acid (ESA-d6) used for comparison may explain the lower ESI efficiency obtained with this reference ligand than for ESA. Overall, this combined strategy demonstrated the preferential gas complex formation of Carbs with ZSA, in agreement with the previously proposed matrix-analyte interaction model that explained ZSA differential efficiency as a MALDI matrix. ZSA + carbohydrate complex preferential formation and higher stability (ESI) support the previously proposed model for ZSA differential efficiency as the MALDI-MS matrix.
doi_str_mv 10.1039/d2nj02789e
format Article
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_d2nj02789e</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>d2nj02789e</sourcerecordid><originalsourceid>FETCH-rsc_primary_d2nj02789e3</originalsourceid><addsrcrecordid>eNqFj0FLAzEQhYNYsLa9eBfmD0ST3XXrnqVSD57ae5lmZ9kpm2SZhNb-e4sWPHp6Dz4-Hk-pB2uerCmb57YIB1MsXxu6UVNb1o1uitreXrqtKm1eqvpO3ad0MMbaZW2nyq82H_pzA0JHwiHBKNSRUMiMA7jox4G-oIviMXMMEDtwKPvYn1vBTAlOnHvQiQOOHNgBOm5_PBRqf2nuCTSn6EnmatJdVmhxzZl6fF9t39ZaktuNwh7lvPv7UP7HvwG0fEvS</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>ESI-MS reveals preferential complex formation of carbohydrates with -sinapinic acid compared with the -isomer</title><source>Royal Society Of Chemistry Journals 2008-</source><source>Alma/SFX Local Collection</source><creator>De León, Tobías Schmidt ; Salum, María Laura ; Matsushita, Yasuyuki ; Fukushima, Kazuhiko ; Monge, María Eugenia ; Erra-Balsells, Rosa</creator><creatorcontrib>De León, Tobías Schmidt ; Salum, María Laura ; Matsushita, Yasuyuki ; Fukushima, Kazuhiko ; Monge, María Eugenia ; Erra-Balsells, Rosa</creatorcontrib><description>Cinnamic acid derivatives including 3,5-dimethoxy-4-hydroxycinnamic acid, also referred to as sinapinic acid (SA), are efficient matrices used in matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). Previous findings have shown that Z -sinapinic acid (ZSA) outperforms E -cinnamic acids for carbohydrate (Carb) analysis, probably due to geometry-induced changes in analyte-matrix interactions at the molecular level, prompted by the cinnamic alkene rigid bond. In the present work, direct infusion electrospray ionization mass spectrometry (DI-ESI-MS) experiments were conducted to investigate the behavior of these acids as ligands for neutral Carb non-covalent complex formation. The ionization efficiency and binding affinities of these small molecules were evaluated towards seven Carbs with different monosaccharide composition and length. Experimental results were interpreted with the assistance of computational calculations. ESA, with higher calculated volume and lower acidity than ZSA, exhibited an experimental ESI efficiency similar to the latter. However, titration experiments showed that the [Acid + Carb] gas complex is preferentially formed with ZSA than ESA when both ligands are present in solution. Results from CID experiments support the formation of more stable complexes between larger Carbs and the ZSA isomer compared to the E -form. The change of molecule volume and polarity in the synthesized isotopically labeled ESA, E -3,5-di(methoxy-d3)-4-hydroxycinnamic acid (ESA-d6) used for comparison may explain the lower ESI efficiency obtained with this reference ligand than for ESA. Overall, this combined strategy demonstrated the preferential gas complex formation of Carbs with ZSA, in agreement with the previously proposed matrix-analyte interaction model that explained ZSA differential efficiency as a MALDI matrix. ZSA + carbohydrate complex preferential formation and higher stability (ESI) support the previously proposed model for ZSA differential efficiency as the MALDI-MS matrix.</description><identifier>ISSN: 1144-0546</identifier><identifier>EISSN: 1369-9261</identifier><identifier>DOI: 10.1039/d2nj02789e</identifier><ispartof>New journal of chemistry, 2022-10, Vol.46 (38), p.18563-18574</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>De León, Tobías Schmidt</creatorcontrib><creatorcontrib>Salum, María Laura</creatorcontrib><creatorcontrib>Matsushita, Yasuyuki</creatorcontrib><creatorcontrib>Fukushima, Kazuhiko</creatorcontrib><creatorcontrib>Monge, María Eugenia</creatorcontrib><creatorcontrib>Erra-Balsells, Rosa</creatorcontrib><title>ESI-MS reveals preferential complex formation of carbohydrates with -sinapinic acid compared with the -isomer</title><title>New journal of chemistry</title><description>Cinnamic acid derivatives including 3,5-dimethoxy-4-hydroxycinnamic acid, also referred to as sinapinic acid (SA), are efficient matrices used in matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). Previous findings have shown that Z -sinapinic acid (ZSA) outperforms E -cinnamic acids for carbohydrate (Carb) analysis, probably due to geometry-induced changes in analyte-matrix interactions at the molecular level, prompted by the cinnamic alkene rigid bond. In the present work, direct infusion electrospray ionization mass spectrometry (DI-ESI-MS) experiments were conducted to investigate the behavior of these acids as ligands for neutral Carb non-covalent complex formation. The ionization efficiency and binding affinities of these small molecules were evaluated towards seven Carbs with different monosaccharide composition and length. Experimental results were interpreted with the assistance of computational calculations. ESA, with higher calculated volume and lower acidity than ZSA, exhibited an experimental ESI efficiency similar to the latter. However, titration experiments showed that the [Acid + Carb] gas complex is preferentially formed with ZSA than ESA when both ligands are present in solution. Results from CID experiments support the formation of more stable complexes between larger Carbs and the ZSA isomer compared to the E -form. The change of molecule volume and polarity in the synthesized isotopically labeled ESA, E -3,5-di(methoxy-d3)-4-hydroxycinnamic acid (ESA-d6) used for comparison may explain the lower ESI efficiency obtained with this reference ligand than for ESA. Overall, this combined strategy demonstrated the preferential gas complex formation of Carbs with ZSA, in agreement with the previously proposed matrix-analyte interaction model that explained ZSA differential efficiency as a MALDI matrix. ZSA + carbohydrate complex preferential formation and higher stability (ESI) support the previously proposed model for ZSA differential efficiency as the MALDI-MS matrix.</description><issn>1144-0546</issn><issn>1369-9261</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFj0FLAzEQhYNYsLa9eBfmD0ST3XXrnqVSD57ae5lmZ9kpm2SZhNb-e4sWPHp6Dz4-Hk-pB2uerCmb57YIB1MsXxu6UVNb1o1uitreXrqtKm1eqvpO3ad0MMbaZW2nyq82H_pzA0JHwiHBKNSRUMiMA7jox4G-oIviMXMMEDtwKPvYn1vBTAlOnHvQiQOOHNgBOm5_PBRqf2nuCTSn6EnmatJdVmhxzZl6fF9t39ZaktuNwh7lvPv7UP7HvwG0fEvS</recordid><startdate>20221003</startdate><enddate>20221003</enddate><creator>De León, Tobías Schmidt</creator><creator>Salum, María Laura</creator><creator>Matsushita, Yasuyuki</creator><creator>Fukushima, Kazuhiko</creator><creator>Monge, María Eugenia</creator><creator>Erra-Balsells, Rosa</creator><scope/></search><sort><creationdate>20221003</creationdate><title>ESI-MS reveals preferential complex formation of carbohydrates with -sinapinic acid compared with the -isomer</title><author>De León, Tobías Schmidt ; Salum, María Laura ; Matsushita, Yasuyuki ; Fukushima, Kazuhiko ; Monge, María Eugenia ; Erra-Balsells, Rosa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_d2nj02789e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2022</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De León, Tobías Schmidt</creatorcontrib><creatorcontrib>Salum, María Laura</creatorcontrib><creatorcontrib>Matsushita, Yasuyuki</creatorcontrib><creatorcontrib>Fukushima, Kazuhiko</creatorcontrib><creatorcontrib>Monge, María Eugenia</creatorcontrib><creatorcontrib>Erra-Balsells, Rosa</creatorcontrib><jtitle>New journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De León, Tobías Schmidt</au><au>Salum, María Laura</au><au>Matsushita, Yasuyuki</au><au>Fukushima, Kazuhiko</au><au>Monge, María Eugenia</au><au>Erra-Balsells, Rosa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ESI-MS reveals preferential complex formation of carbohydrates with -sinapinic acid compared with the -isomer</atitle><jtitle>New journal of chemistry</jtitle><date>2022-10-03</date><risdate>2022</risdate><volume>46</volume><issue>38</issue><spage>18563</spage><epage>18574</epage><pages>18563-18574</pages><issn>1144-0546</issn><eissn>1369-9261</eissn><abstract>Cinnamic acid derivatives including 3,5-dimethoxy-4-hydroxycinnamic acid, also referred to as sinapinic acid (SA), are efficient matrices used in matrix assisted laser desorption/ionization mass spectrometry (MALDI-MS). Previous findings have shown that Z -sinapinic acid (ZSA) outperforms E -cinnamic acids for carbohydrate (Carb) analysis, probably due to geometry-induced changes in analyte-matrix interactions at the molecular level, prompted by the cinnamic alkene rigid bond. In the present work, direct infusion electrospray ionization mass spectrometry (DI-ESI-MS) experiments were conducted to investigate the behavior of these acids as ligands for neutral Carb non-covalent complex formation. The ionization efficiency and binding affinities of these small molecules were evaluated towards seven Carbs with different monosaccharide composition and length. Experimental results were interpreted with the assistance of computational calculations. ESA, with higher calculated volume and lower acidity than ZSA, exhibited an experimental ESI efficiency similar to the latter. However, titration experiments showed that the [Acid + Carb] gas complex is preferentially formed with ZSA than ESA when both ligands are present in solution. Results from CID experiments support the formation of more stable complexes between larger Carbs and the ZSA isomer compared to the E -form. The change of molecule volume and polarity in the synthesized isotopically labeled ESA, E -3,5-di(methoxy-d3)-4-hydroxycinnamic acid (ESA-d6) used for comparison may explain the lower ESI efficiency obtained with this reference ligand than for ESA. Overall, this combined strategy demonstrated the preferential gas complex formation of Carbs with ZSA, in agreement with the previously proposed matrix-analyte interaction model that explained ZSA differential efficiency as a MALDI matrix. ZSA + carbohydrate complex preferential formation and higher stability (ESI) support the previously proposed model for ZSA differential efficiency as the MALDI-MS matrix.</abstract><doi>10.1039/d2nj02789e</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1144-0546
ispartof New journal of chemistry, 2022-10, Vol.46 (38), p.18563-18574
issn 1144-0546
1369-9261
language
recordid cdi_rsc_primary_d2nj02789e
source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
title ESI-MS reveals preferential complex formation of carbohydrates with -sinapinic acid compared with the -isomer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T10%3A54%3A26IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ESI-MS%20reveals%20preferential%20complex%20formation%20of%20carbohydrates%20with%20-sinapinic%20acid%20compared%20with%20the%20-isomer&rft.jtitle=New%20journal%20of%20chemistry&rft.au=De%20Le%C3%B3n,%20Tob%C3%ADas%20Schmidt&rft.date=2022-10-03&rft.volume=46&rft.issue=38&rft.spage=18563&rft.epage=18574&rft.pages=18563-18574&rft.issn=1144-0546&rft.eissn=1369-9261&rft_id=info:doi/10.1039/d2nj02789e&rft_dat=%3Crsc%3Ed2nj02789e%3C/rsc%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true