Identification and characterization of reaction products of 5‐hydroxytryptamine with methylglyoxal and glyoxal by liquid chromatography/tandem mass spectrometry
Rationale Methylglyoxal (MGO) and glyoxal (GO) are known to be at high levels in humans with diabetes. They react with amine‐containing proteins and amino acids to form advanced glycation end products, however, their reactivity with other amine‐containing metabolites, such as neurotransmitters, has...
Gespeichert in:
Veröffentlicht in: | Rapid communications in mass spectrometry 2018-09, Vol.32 (17), p.1529-1539 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1539 |
---|---|
container_issue | 17 |
container_start_page | 1529 |
container_title | Rapid communications in mass spectrometry |
container_volume | 32 |
creator | Sai Sachin, L. Nagarjuna Chary, R. Pavankumar, P. Prabhakar, S. |
description | Rationale
Methylglyoxal (MGO) and glyoxal (GO) are known to be at high levels in humans with diabetes. They react with amine‐containing proteins and amino acids to form advanced glycation end products, however, their reactivity with other amine‐containing metabolites, such as neurotransmitters, has not been explored. In this study, we aimed at studying the reactivity of 5‐hydroxytryptamine (5‐HT) with MGO or GO, which may alter the metabolic function of 5‐HT.
Methods
Stock solutions of 5‐HT, MGO and GO were made in PBS buffer at pH 7.4 and 5‐HT was incubated with MGO or GO at different concentrations. The reactions were also performed at physiological concentrations. The reaction mixtures collected at different incubation times were analyzed by direct ESI‐HRMS, LC/MS and LC/MS/MS to detect/characterize the products. Agilent 6545 Q‐TOF and Agilent 6420 triple quadrupole mass spectrometers were used for the study, and LC separations were performed on a C18 column.
Results
The direct ESI‐HRMS data of the reaction mixtures showed formation of three and four reaction products when 5‐HT was reacted with MGO and GO, respectively. All the products showed dominant [M + H]+ ions. The products were characterized by HRMS, LC/MS/MS and literature reports on similar compounds. The products can easily be identified by LC/MS based on the accurate mass values together with retention time information. The MS/MS of the reaction products showed structure‐indicative fragment ions.
Conclusions
5‐HT reacts with one or two MGO/GO to form a set of reaction products. The reaction between 5‐HT and MGO or GO was faster at higher concentrations of MGO/GO ( |
doi_str_mv | 10.1002/rcm.8195 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2051671168</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2083535501</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3495-5fd4bd904faf5391b9ec7ee368d536f26ee7982151d0bfd9c529162a5a343b0a3</originalsourceid><addsrcrecordid>eNp1kd9q1jAYh4Mo7nMKXoEUPPGkW_40bXMoH1MHE0H0uKTJmzWjabokZatHXoLX4KV5Jab7NgXBo7z88vDkDT-EXhJ8QjCmp0G5k5YI_gjtCBZNiSkjj9EOC07Kioj2CD2L8QpjQjjFT9ERFW1TVZjt0M9zDVOyxiqZrJ8KOelCDTJIlSDYb4fQmyJATrZ5Dl4vKsUt5L--_xhWHfztmsI6J-nsBMWNTUPhIA3reDmu_laOd9aHuV-L0V4vdnsneCeTvwxyHtbTlClwhZMxFnEGlfItZO9z9MTIMcKL-_MYfX139mX_obz49P58__aiVKwSvORGV70WuDLScCZIL0A1AKxuNWe1oTVAI1pKONG4N1ooTgWpqeSSVazHkh2jNwdv_uL1AjF1zkYF4ygn8EvsKOakbgip24y-_ge98kuY8naZahlnnGPyV6iCjzGA6eZgnQxrR3C39dbl3rqtt4y-uhcuvQP9B3woKgPlAbixI6z_FXWf9x_vhL8B2q-nRA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2083535501</pqid></control><display><type>article</type><title>Identification and characterization of reaction products of 5‐hydroxytryptamine with methylglyoxal and glyoxal by liquid chromatography/tandem mass spectrometry</title><source>Wiley Online Library All Journals</source><creator>Sai Sachin, L. ; Nagarjuna Chary, R. ; Pavankumar, P. ; Prabhakar, S.</creator><creatorcontrib>Sai Sachin, L. ; Nagarjuna Chary, R. ; Pavankumar, P. ; Prabhakar, S.</creatorcontrib><description>Rationale
Methylglyoxal (MGO) and glyoxal (GO) are known to be at high levels in humans with diabetes. They react with amine‐containing proteins and amino acids to form advanced glycation end products, however, their reactivity with other amine‐containing metabolites, such as neurotransmitters, has not been explored. In this study, we aimed at studying the reactivity of 5‐hydroxytryptamine (5‐HT) with MGO or GO, which may alter the metabolic function of 5‐HT.
Methods
Stock solutions of 5‐HT, MGO and GO were made in PBS buffer at pH 7.4 and 5‐HT was incubated with MGO or GO at different concentrations. The reactions were also performed at physiological concentrations. The reaction mixtures collected at different incubation times were analyzed by direct ESI‐HRMS, LC/MS and LC/MS/MS to detect/characterize the products. Agilent 6545 Q‐TOF and Agilent 6420 triple quadrupole mass spectrometers were used for the study, and LC separations were performed on a C18 column.
Results
The direct ESI‐HRMS data of the reaction mixtures showed formation of three and four reaction products when 5‐HT was reacted with MGO and GO, respectively. All the products showed dominant [M + H]+ ions. The products were characterized by HRMS, LC/MS/MS and literature reports on similar compounds. The products can easily be identified by LC/MS based on the accurate mass values together with retention time information. The MS/MS of the reaction products showed structure‐indicative fragment ions.
Conclusions
5‐HT reacts with one or two MGO/GO to form a set of reaction products. The reaction between 5‐HT and MGO or GO was faster at higher concentrations of MGO/GO (<10 min), and the same products were found even at physiological concentrations (<48 h). The LC/MS/MS (SRM) method can be used to screen the reaction products when present at low levels.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.8195</identifier><identifier>PMID: 29874403</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Amino acids ; Columns (structural) ; Diabetes ; Liquid chromatography ; Mass spectrometers ; Mass spectrometry ; Metabolites ; Neurotransmitters ; Physiology ; Proteins ; Quadrupoles ; Reaction products ; Spectrometers</subject><ispartof>Rapid communications in mass spectrometry, 2018-09, Vol.32 (17), p.1529-1539</ispartof><rights>2018 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3495-5fd4bd904faf5391b9ec7ee368d536f26ee7982151d0bfd9c529162a5a343b0a3</citedby><cites>FETCH-LOGICAL-c3495-5fd4bd904faf5391b9ec7ee368d536f26ee7982151d0bfd9c529162a5a343b0a3</cites><orcidid>0000-0003-0922-6762</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Frcm.8195$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Frcm.8195$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29874403$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sai Sachin, L.</creatorcontrib><creatorcontrib>Nagarjuna Chary, R.</creatorcontrib><creatorcontrib>Pavankumar, P.</creatorcontrib><creatorcontrib>Prabhakar, S.</creatorcontrib><title>Identification and characterization of reaction products of 5‐hydroxytryptamine with methylglyoxal and glyoxal by liquid chromatography/tandem mass spectrometry</title><title>Rapid communications in mass spectrometry</title><addtitle>Rapid Commun Mass Spectrom</addtitle><description>Rationale
Methylglyoxal (MGO) and glyoxal (GO) are known to be at high levels in humans with diabetes. They react with amine‐containing proteins and amino acids to form advanced glycation end products, however, their reactivity with other amine‐containing metabolites, such as neurotransmitters, has not been explored. In this study, we aimed at studying the reactivity of 5‐hydroxytryptamine (5‐HT) with MGO or GO, which may alter the metabolic function of 5‐HT.
Methods
Stock solutions of 5‐HT, MGO and GO were made in PBS buffer at pH 7.4 and 5‐HT was incubated with MGO or GO at different concentrations. The reactions were also performed at physiological concentrations. The reaction mixtures collected at different incubation times were analyzed by direct ESI‐HRMS, LC/MS and LC/MS/MS to detect/characterize the products. Agilent 6545 Q‐TOF and Agilent 6420 triple quadrupole mass spectrometers were used for the study, and LC separations were performed on a C18 column.
Results
The direct ESI‐HRMS data of the reaction mixtures showed formation of three and four reaction products when 5‐HT was reacted with MGO and GO, respectively. All the products showed dominant [M + H]+ ions. The products were characterized by HRMS, LC/MS/MS and literature reports on similar compounds. The products can easily be identified by LC/MS based on the accurate mass values together with retention time information. The MS/MS of the reaction products showed structure‐indicative fragment ions.
Conclusions
5‐HT reacts with one or two MGO/GO to form a set of reaction products. The reaction between 5‐HT and MGO or GO was faster at higher concentrations of MGO/GO (<10 min), and the same products were found even at physiological concentrations (<48 h). The LC/MS/MS (SRM) method can be used to screen the reaction products when present at low levels.</description><subject>Amino acids</subject><subject>Columns (structural)</subject><subject>Diabetes</subject><subject>Liquid chromatography</subject><subject>Mass spectrometers</subject><subject>Mass spectrometry</subject><subject>Metabolites</subject><subject>Neurotransmitters</subject><subject>Physiology</subject><subject>Proteins</subject><subject>Quadrupoles</subject><subject>Reaction products</subject><subject>Spectrometers</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kd9q1jAYh4Mo7nMKXoEUPPGkW_40bXMoH1MHE0H0uKTJmzWjabokZatHXoLX4KV5Jab7NgXBo7z88vDkDT-EXhJ8QjCmp0G5k5YI_gjtCBZNiSkjj9EOC07Kioj2CD2L8QpjQjjFT9ERFW1TVZjt0M9zDVOyxiqZrJ8KOelCDTJIlSDYb4fQmyJATrZ5Dl4vKsUt5L--_xhWHfztmsI6J-nsBMWNTUPhIA3reDmu_laOd9aHuV-L0V4vdnsneCeTvwxyHtbTlClwhZMxFnEGlfItZO9z9MTIMcKL-_MYfX139mX_obz49P58__aiVKwSvORGV70WuDLScCZIL0A1AKxuNWe1oTVAI1pKONG4N1ooTgWpqeSSVazHkh2jNwdv_uL1AjF1zkYF4ygn8EvsKOakbgip24y-_ge98kuY8naZahlnnGPyV6iCjzGA6eZgnQxrR3C39dbl3rqtt4y-uhcuvQP9B3woKgPlAbixI6z_FXWf9x_vhL8B2q-nRA</recordid><startdate>20180915</startdate><enddate>20180915</enddate><creator>Sai Sachin, L.</creator><creator>Nagarjuna Chary, R.</creator><creator>Pavankumar, P.</creator><creator>Prabhakar, S.</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>JQ2</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0922-6762</orcidid></search><sort><creationdate>20180915</creationdate><title>Identification and characterization of reaction products of 5‐hydroxytryptamine with methylglyoxal and glyoxal by liquid chromatography/tandem mass spectrometry</title><author>Sai Sachin, L. ; Nagarjuna Chary, R. ; Pavankumar, P. ; Prabhakar, S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3495-5fd4bd904faf5391b9ec7ee368d536f26ee7982151d0bfd9c529162a5a343b0a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Amino acids</topic><topic>Columns (structural)</topic><topic>Diabetes</topic><topic>Liquid chromatography</topic><topic>Mass spectrometers</topic><topic>Mass spectrometry</topic><topic>Metabolites</topic><topic>Neurotransmitters</topic><topic>Physiology</topic><topic>Proteins</topic><topic>Quadrupoles</topic><topic>Reaction products</topic><topic>Spectrometers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sai Sachin, L.</creatorcontrib><creatorcontrib>Nagarjuna Chary, R.</creatorcontrib><creatorcontrib>Pavankumar, P.</creatorcontrib><creatorcontrib>Prabhakar, S.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sai Sachin, L.</au><au>Nagarjuna Chary, R.</au><au>Pavankumar, P.</au><au>Prabhakar, S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and characterization of reaction products of 5‐hydroxytryptamine with methylglyoxal and glyoxal by liquid chromatography/tandem mass spectrometry</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><addtitle>Rapid Commun Mass Spectrom</addtitle><date>2018-09-15</date><risdate>2018</risdate><volume>32</volume><issue>17</issue><spage>1529</spage><epage>1539</epage><pages>1529-1539</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>Rationale
Methylglyoxal (MGO) and glyoxal (GO) are known to be at high levels in humans with diabetes. They react with amine‐containing proteins and amino acids to form advanced glycation end products, however, their reactivity with other amine‐containing metabolites, such as neurotransmitters, has not been explored. In this study, we aimed at studying the reactivity of 5‐hydroxytryptamine (5‐HT) with MGO or GO, which may alter the metabolic function of 5‐HT.
Methods
Stock solutions of 5‐HT, MGO and GO were made in PBS buffer at pH 7.4 and 5‐HT was incubated with MGO or GO at different concentrations. The reactions were also performed at physiological concentrations. The reaction mixtures collected at different incubation times were analyzed by direct ESI‐HRMS, LC/MS and LC/MS/MS to detect/characterize the products. Agilent 6545 Q‐TOF and Agilent 6420 triple quadrupole mass spectrometers were used for the study, and LC separations were performed on a C18 column.
Results
The direct ESI‐HRMS data of the reaction mixtures showed formation of three and four reaction products when 5‐HT was reacted with MGO and GO, respectively. All the products showed dominant [M + H]+ ions. The products were characterized by HRMS, LC/MS/MS and literature reports on similar compounds. The products can easily be identified by LC/MS based on the accurate mass values together with retention time information. The MS/MS of the reaction products showed structure‐indicative fragment ions.
Conclusions
5‐HT reacts with one or two MGO/GO to form a set of reaction products. The reaction between 5‐HT and MGO or GO was faster at higher concentrations of MGO/GO (<10 min), and the same products were found even at physiological concentrations (<48 h). The LC/MS/MS (SRM) method can be used to screen the reaction products when present at low levels.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29874403</pmid><doi>10.1002/rcm.8195</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-0922-6762</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0951-4198 |
ispartof | Rapid communications in mass spectrometry, 2018-09, Vol.32 (17), p.1529-1539 |
issn | 0951-4198 1097-0231 |
language | eng |
recordid | cdi_proquest_miscellaneous_2051671168 |
source | Wiley Online Library All Journals |
subjects | Amino acids Columns (structural) Diabetes Liquid chromatography Mass spectrometers Mass spectrometry Metabolites Neurotransmitters Physiology Proteins Quadrupoles Reaction products Spectrometers |
title | Identification and characterization of reaction products of 5‐hydroxytryptamine with methylglyoxal and glyoxal by liquid chromatography/tandem mass spectrometry |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T10%3A37%3A38IST&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=Identification%20and%20characterization%20of%20reaction%20products%20of%205%E2%80%90hydroxytryptamine%20with%20methylglyoxal%20and%20glyoxal%20by%20liquid%20chromatography/tandem%20mass%20spectrometry&rft.jtitle=Rapid%20communications%20in%20mass%20spectrometry&rft.au=Sai%20Sachin,%20L.&rft.date=2018-09-15&rft.volume=32&rft.issue=17&rft.spage=1529&rft.epage=1539&rft.pages=1529-1539&rft.issn=0951-4198&rft.eissn=1097-0231&rft_id=info:doi/10.1002/rcm.8195&rft_dat=%3Cproquest_cross%3E2083535501%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=2083535501&rft_id=info:pmid/29874403&rfr_iscdi=true |