16952279

pubmed:Citation

1

The activity and levels of the metazoan HIF (hypoxia-inducible factor) are regulated by its hydroxylation, catalysed by 2OG (2-oxoglutarate)- and Fe(II)-dependent dioxygenases. An oxygen consumption assay was developed and used to study the relationship between HIF hydroxylase activity and oxygen concentration for recombinant forms of two human HIF hydroxylases, PHD2 (prolyl hydroxylase domain-containing protein 2) and FIH (factor inhibiting HIF), and compared with two other 2OG-dependent dioxygenases. Although there are caveats on the absolute values, the apparent K(m) (oxygen) values for PHD2 and FIH were within the range observed for other 2OG oxygenases. Recombinant protein substrates were found to have lower apparent K(m) (oxygen) values compared with shorter synthetic peptides of HIF. The analyses also suggest that human PHD2 is selective for fragments of the C-terminal over the N-terminal oxygen-dependent degradation domain of HIF-1alpha. The present results, albeit obtained under non-physiological conditions, imply that the apparent K(m) (oxygen) values of the HIF hydroxylases enable them to act as oxygen sensors providing their in vivo capacity is appropriately matched to a hydroxylation-sensitive signalling pathway.

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http://linkedlifedata.com/resource/pubmed/journal/2984726R

http://linkedlifedata.com/resource/pubmed/chemical/EGLN1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Glucose Oxidase, http://linkedlifedata.com/resource/pubmed/chemical/HIF1AN protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Mixed Function Oxygenases, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments, http://linkedlifedata.com/resource/pubmed/chemical/Procollagen-Proline Dioxygenase, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors

Jan

pubmed-author:EhrismannDominicD, pubmed-author:FlashmanEmilyE, pubmed-author:GennDavid NDN, pubmed-author:HewitsonKirsty SKS, pubmed-author:MathioudakisNicolasN, pubmed-author:RatcliffePeter JPJ, pubmed-author:SchofieldChristopher JCJ

1

NLM

227-34

pubmed-meshheading:16952279-Cloning, Molecular, pubmed-meshheading:16952279-Glucose Oxidase, pubmed-meshheading:16952279-Kinetics, pubmed-meshheading:16952279-Mixed Function Oxygenases, pubmed-meshheading:16952279-Oxygen Consumption, pubmed-meshheading:16952279-Peptide Fragments, pubmed-meshheading:16952279-Procollagen-Proline Dioxygenase, pubmed-meshheading:16952279-Protein Binding, pubmed-meshheading:16952279-Recombinant Proteins, pubmed-meshheading:16952279-Repressor Proteins, pubmed-meshheading:16952279-Substrate Specificity, pubmed-meshheading:16952279-Transcription Factors

Studies on the activity of the hypoxia-inducible-factor hydroxylases using an oxygen consumption assay.

Journal Article, Research Support, Non-U.S. Gov't