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Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma
To identify biomarkers of ethyl (1-(diethylamino)ethylidene)phosphoramidofluoridate (A234)- or methyl (1-(diethylamino)ethylidene)phosphoramidofluoridate (A232)-inhibited butyrylcholinesterase (BChE), we investigated nonapeptide adducts containing the active site serine, which plays a key role in en...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270327/ https://www.ncbi.nlm.nih.gov/pubmed/34206601 http://dx.doi.org/10.3390/molecules26133810 |
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author | Jeong, Woo-Hyeon Lee, Jin-Young Lim, Kyoung-Chan Kim, Hyun-Suk |
author_facet | Jeong, Woo-Hyeon Lee, Jin-Young Lim, Kyoung-Chan Kim, Hyun-Suk |
author_sort | Jeong, Woo-Hyeon |
collection | PubMed |
description | To identify biomarkers of ethyl (1-(diethylamino)ethylidene)phosphoramidofluoridate (A234)- or methyl (1-(diethylamino)ethylidene)phosphoramidofluoridate (A232)-inhibited butyrylcholinesterase (BChE), we investigated nonapeptide adducts containing the active site serine, which plays a key role in enzyme activity, using LC-MS/HRMS. Biomarkers were acquired as expected, and they exhibited a significant amount of fragment ions from the inhibiting agent itself, in contrast to the MS2 spectra of conventional nerve agents. These biomarkers had a higher abundance of [M+2H](2+) ions than [M+H](+) ions, making doubly charged ions more suitable for trace analysis. |
format | Online Article Text |
id | pubmed-8270327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82703272021-07-10 Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma Jeong, Woo-Hyeon Lee, Jin-Young Lim, Kyoung-Chan Kim, Hyun-Suk Molecules Article To identify biomarkers of ethyl (1-(diethylamino)ethylidene)phosphoramidofluoridate (A234)- or methyl (1-(diethylamino)ethylidene)phosphoramidofluoridate (A232)-inhibited butyrylcholinesterase (BChE), we investigated nonapeptide adducts containing the active site serine, which plays a key role in enzyme activity, using LC-MS/HRMS. Biomarkers were acquired as expected, and they exhibited a significant amount of fragment ions from the inhibiting agent itself, in contrast to the MS2 spectra of conventional nerve agents. These biomarkers had a higher abundance of [M+2H](2+) ions than [M+H](+) ions, making doubly charged ions more suitable for trace analysis. MDPI 2021-06-22 /pmc/articles/PMC8270327/ /pubmed/34206601 http://dx.doi.org/10.3390/molecules26133810 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jeong, Woo-Hyeon Lee, Jin-Young Lim, Kyoung-Chan Kim, Hyun-Suk Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma |
title | Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma |
title_full | Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma |
title_fullStr | Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma |
title_full_unstemmed | Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma |
title_short | Identification and Study of Biomarkers from Novichok-Inhibited Butyrylcholinesterase in Human Plasma |
title_sort | identification and study of biomarkers from novichok-inhibited butyrylcholinesterase in human plasma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270327/ https://www.ncbi.nlm.nih.gov/pubmed/34206601 http://dx.doi.org/10.3390/molecules26133810 |
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