Inhibition of a prolyl hydroxylase domain (PHD) by substrate analog peptides

Authors
Kwon, Hyuk SungChoi, Yien KyoungKim, Jeong WonPark, Yong KeunYang, Eun GyeongAhn, Dae-Ro
Issue Date
2011-07-15
Publisher
Pergamon Press Ltd.
Citation
Bioorganic & Medicinal Chemistry Letters, v.21, no.14, pp.4325 - 4328
Abstract
Oxygen dependent degradation of hypoxia-inducible factor (HIF)-1 alpha is triggered with hydroxylation by proline hydroxylase domain 2 (PHD2) under normoxic conditions. Some of previously developed PHD2 inhibitors show a considerable potency against factor inhibiting HIF (FIH), the HIF asparagine hydroxylase. For specific inhibition of PHD2, we have synthesized peptides containing 556-575 residues of HIF-1 alpha with modifications at the Pro-564 and examined their inhibitory effect against PHD2. Adopting fluorescence polarization-based assays, we evaluated inhibitory potency of the peptides and selected potent inhibitors. These PHD2 inhibitor peptides showed no significant potency against FIH, demonstrating their specific inhibitory effect on PHD2. (C) 2011 Elsevier Ltd. All rights reserved.
Keywords
HIF; HIF-1-ALPHA; REVEALS; HIF; HIF-1-ALPHA; REVEALS; HIF-1 alpha; PHD2; Substrate analog peptides; Peptide inhibitors; Hypoxia
ISSN
0960-894X
URI
https://pubs.kist.re.kr/handle/201004/130180
DOI
10.1016/j.bmcl.2011.05.050
Appears in Collections:
KIST Article > 2011
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