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New luciferin-based probe substrates for human CYP26A1

Activity of human CYP26A1 towards six proluciferin probe substrates and their ester derivatives was monitored. These included three monofluorobenzyl ether isomers and three five-membered heterocycles. Overall, luciferin substrates with a free acid group gave higher activities than the ester compound...

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Autores principales: Sharma, Shishir, Liu, Jingyao, Zhang, Xue, Sharma, Sangeeta Shrestha, Sorensen, Erik J., Bureik, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695906/
https://www.ncbi.nlm.nih.gov/pubmed/33294638
http://dx.doi.org/10.1016/j.bbrep.2020.100861
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author Sharma, Shishir
Liu, Jingyao
Zhang, Xue
Sharma, Sangeeta Shrestha
Sorensen, Erik J.
Bureik, Matthias
author_facet Sharma, Shishir
Liu, Jingyao
Zhang, Xue
Sharma, Sangeeta Shrestha
Sorensen, Erik J.
Bureik, Matthias
author_sort Sharma, Shishir
collection PubMed
description Activity of human CYP26A1 towards six proluciferin probe substrates and their ester derivatives was monitored. These included three monofluorobenzyl ether isomers and three five-membered heterocycles. Overall, luciferin substrates with a free acid group gave higher activities than the ester compounds. Also, luciferin derivatives with six-ring structures were better metabolized than those with five-rings. The best substrates identified in this study are Luciferin 6′ 3-fluorobenzyl ether (Luciferin-3FBE) and its methyl ester (Luciferin-3FBEME). Taken together, we describe eleven new probe substrates for CYP26A1 and demonstrate for the first time that CYP26A1 does not only accept acid substrates but can also metabolize esters.
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spelling pubmed-76959062020-12-07 New luciferin-based probe substrates for human CYP26A1 Sharma, Shishir Liu, Jingyao Zhang, Xue Sharma, Sangeeta Shrestha Sorensen, Erik J. Bureik, Matthias Biochem Biophys Rep Research Article Activity of human CYP26A1 towards six proluciferin probe substrates and their ester derivatives was monitored. These included three monofluorobenzyl ether isomers and three five-membered heterocycles. Overall, luciferin substrates with a free acid group gave higher activities than the ester compounds. Also, luciferin derivatives with six-ring structures were better metabolized than those with five-rings. The best substrates identified in this study are Luciferin 6′ 3-fluorobenzyl ether (Luciferin-3FBE) and its methyl ester (Luciferin-3FBEME). Taken together, we describe eleven new probe substrates for CYP26A1 and demonstrate for the first time that CYP26A1 does not only accept acid substrates but can also metabolize esters. Elsevier 2020-11-23 /pmc/articles/PMC7695906/ /pubmed/33294638 http://dx.doi.org/10.1016/j.bbrep.2020.100861 Text en © 2020 Published by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Sharma, Shishir
Liu, Jingyao
Zhang, Xue
Sharma, Sangeeta Shrestha
Sorensen, Erik J.
Bureik, Matthias
New luciferin-based probe substrates for human CYP26A1
title New luciferin-based probe substrates for human CYP26A1
title_full New luciferin-based probe substrates for human CYP26A1
title_fullStr New luciferin-based probe substrates for human CYP26A1
title_full_unstemmed New luciferin-based probe substrates for human CYP26A1
title_short New luciferin-based probe substrates for human CYP26A1
title_sort new luciferin-based probe substrates for human cyp26a1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695906/
https://www.ncbi.nlm.nih.gov/pubmed/33294638
http://dx.doi.org/10.1016/j.bbrep.2020.100861
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