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A new derivative for oxosteroid analysis by mass spectrometry

Here we report a new method for oxosteroid identification utilizing “tandem mass tag hydrazine” (TMTH) carbonyl-reactive derivatisation reagent. TMTH is a reagent with a chargeable tertiary amino group attached through a linker to a carbonyl-reactive hydrazine group. Thirty oxosteroids were analysed...

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Detalles Bibliográficos
Autores principales: Rigdova, K., Wang, Y., Ward, M., Griffiths, W.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000438/
https://www.ncbi.nlm.nih.gov/pubmed/24525129
http://dx.doi.org/10.1016/j.bbrc.2014.01.190
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author Rigdova, K.
Wang, Y.
Ward, M.
Griffiths, W.J.
author_facet Rigdova, K.
Wang, Y.
Ward, M.
Griffiths, W.J.
author_sort Rigdova, K.
collection PubMed
description Here we report a new method for oxosteroid identification utilizing “tandem mass tag hydrazine” (TMTH) carbonyl-reactive derivatisation reagent. TMTH is a reagent with a chargeable tertiary amino group attached through a linker to a carbonyl-reactive hydrazine group. Thirty oxosteroids were analysed after derivatisation with TMTH by electrospray ionization mass spectrometry (ESI-MS) and were found to give high ion-currents compared to underivatised molecules. ESI-tandem mass spectrometry (MS/MS) analysis of the derivatives yielded characteristic fragmentation patterns with specific mass reporter ions derived from the TMT group. A shotgun ESI-MS method incorporating TMTH derivatisation was applied to a urine sample.
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spelling pubmed-40004382014-04-28 A new derivative for oxosteroid analysis by mass spectrometry Rigdova, K. Wang, Y. Ward, M. Griffiths, W.J. Biochem Biophys Res Commun Article Here we report a new method for oxosteroid identification utilizing “tandem mass tag hydrazine” (TMTH) carbonyl-reactive derivatisation reagent. TMTH is a reagent with a chargeable tertiary amino group attached through a linker to a carbonyl-reactive hydrazine group. Thirty oxosteroids were analysed after derivatisation with TMTH by electrospray ionization mass spectrometry (ESI-MS) and were found to give high ion-currents compared to underivatised molecules. ESI-tandem mass spectrometry (MS/MS) analysis of the derivatives yielded characteristic fragmentation patterns with specific mass reporter ions derived from the TMT group. A shotgun ESI-MS method incorporating TMTH derivatisation was applied to a urine sample. Academic Press 2014-04-11 /pmc/articles/PMC4000438/ /pubmed/24525129 http://dx.doi.org/10.1016/j.bbrc.2014.01.190 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Rigdova, K.
Wang, Y.
Ward, M.
Griffiths, W.J.
A new derivative for oxosteroid analysis by mass spectrometry
title A new derivative for oxosteroid analysis by mass spectrometry
title_full A new derivative for oxosteroid analysis by mass spectrometry
title_fullStr A new derivative for oxosteroid analysis by mass spectrometry
title_full_unstemmed A new derivative for oxosteroid analysis by mass spectrometry
title_short A new derivative for oxosteroid analysis by mass spectrometry
title_sort new derivative for oxosteroid analysis by mass spectrometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000438/
https://www.ncbi.nlm.nih.gov/pubmed/24525129
http://dx.doi.org/10.1016/j.bbrc.2014.01.190
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