Determination and comparison of specific activity of the HIF‐prolyl hydroxylases

FEBS Letters - Tập 576 Số 1-2 - Trang 145-150 - 2004
Jason R. Tuckerman1, Yuguang Zhao1, Kirsty S. Hewitson2, Ya‐Min Tian1, Christopher W. Pugh1, Peter J. Ratcliffe1, David R. Mole1
1Henry Wellcome Building for Genomic Medicine, Roosevelt Drive, Oxford OX3 7BN, UK
2Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, UK

Tóm tắt

Hypoxia‐inducible factor (HIF) is a transcriptional complex that is regulated by oxygen sensitive hydroxylation of its α subunits by the prolyl hydroxylases PHD1, 2 and 3. To better understand the role of these enzymes in directing cellular responses to hypoxia, we derived an assay to determine their specific activity in both native cell extracts and recombinant sources of enzyme. We show that all three are capable of high rates of catalysis, in the order PHD2=PHD3 > PHD1, using substrate peptides derived from the C‐terminal degradation domain of HIF‐α subunits, and that each demonstrates similar and remarkable sensitivity to oxygen, commensurate with a common role in signaling hypoxia.

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