A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging

Prolyl hydroxylation domain (PHD) enzymes catalyze the hydroxylation of the transcription factor hypoxia‐inducible factor (HIF) and serve as cellular oxygen sensors. HIF and the PHD enzymes regulate numerous potentially tissue‐protective target genes which can adapt cells to metabolic and ischemic s...

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Автори: Mayer, M, Fey, K, Heinze, E, Rainer Wick, C, Abboud, M, Yeh, T, Tumber, A, Orth, N, Schley, G, Buchholz, B, Clark, T, Schofield, C, Willam, C, Burzlaff, N
Формат: Journal article
Опубліковано: Wiley 2018
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author Mayer, M
Fey, K
Heinze, E
Rainer Wick, C
Abboud, M
Yeh, T
Tumber, A
Orth, N
Schley, G
Buchholz, B
Clark, T
Schofield, C
Willam, C
Burzlaff, N
author_facet Mayer, M
Fey, K
Heinze, E
Rainer Wick, C
Abboud, M
Yeh, T
Tumber, A
Orth, N
Schley, G
Buchholz, B
Clark, T
Schofield, C
Willam, C
Burzlaff, N
author_sort Mayer, M
collection OXFORD
description Prolyl hydroxylation domain (PHD) enzymes catalyze the hydroxylation of the transcription factor hypoxia‐inducible factor (HIF) and serve as cellular oxygen sensors. HIF and the PHD enzymes regulate numerous potentially tissue‐protective target genes which can adapt cells to metabolic and ischemic stress. We describe a fluorescent PHD inhibitor (1‐chloro‐4‐hydroxybenzo[g]isoquinoline‐3‐carbonyl)glycine which is suited to fluorescence‐based detection assays and for monitoring PHD inhibitors in biological systems. In cell‐based assays, application of the fluorescent PHD inhibitor allowed co‐localization with a cellular PHD enzyme and led to live cell imaging of processes involved in cellular oxygen sensing.
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spelling oxford-uuid:09c12867-94e2-435e-b6b3-79cae589126b2022-03-26T09:20:03ZA fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imagingJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:09c12867-94e2-435e-b6b3-79cae589126bSymplectic Elements at OxfordWiley2018Mayer, MFey, KHeinze, ERainer Wick, CAbboud, MYeh, TTumber, AOrth, NSchley, GBuchholz, BClark, TSchofield, CWillam, CBurzlaff, NProlyl hydroxylation domain (PHD) enzymes catalyze the hydroxylation of the transcription factor hypoxia‐inducible factor (HIF) and serve as cellular oxygen sensors. HIF and the PHD enzymes regulate numerous potentially tissue‐protective target genes which can adapt cells to metabolic and ischemic stress. We describe a fluorescent PHD inhibitor (1‐chloro‐4‐hydroxybenzo[g]isoquinoline‐3‐carbonyl)glycine which is suited to fluorescence‐based detection assays and for monitoring PHD inhibitors in biological systems. In cell‐based assays, application of the fluorescent PHD inhibitor allowed co‐localization with a cellular PHD enzyme and led to live cell imaging of processes involved in cellular oxygen sensing.
spellingShingle Mayer, M
Fey, K
Heinze, E
Rainer Wick, C
Abboud, M
Yeh, T
Tumber, A
Orth, N
Schley, G
Buchholz, B
Clark, T
Schofield, C
Willam, C
Burzlaff, N
A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging
title A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging
title_full A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging
title_fullStr A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging
title_full_unstemmed A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging
title_short A fluorescent benzo[g]isoquinoline-based HIF prolyl hydroxylase inhibitor for cellular imaging
title_sort fluorescent benzo g isoquinoline based hif prolyl hydroxylase inhibitor for cellular imaging
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