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...

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Veröffentlicht in:Rapid communications in mass spectrometry 2018-09, Vol.32 (17), p.1529-1539
Hauptverfasser: Sai Sachin, L., Nagarjuna Chary, R., Pavankumar, P., Prabhakar, S.
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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 (
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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 (&lt;10 min), and the same products were found even at physiological concentrations (&lt;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 &amp; 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 (&lt;10 min), and the same products were found even at physiological concentrations (&lt;48 h). 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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 (&lt;10 min), and the same products were found even at physiological concentrations (&lt;48 h). 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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
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