Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, United Kingdom.
Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford OX1 3TA, United Kingdom.
Bioorg Med Chem. 2019 Jun 15;27(12):2405-2412. doi: 10.1016/j.bmc.2019.01.018. Epub 2019 Jan 23.
The hydroxylation of prolyl-residues in eukaryotes is important in collagen biosynthesis and in hypoxic signalling. The hypoxia inducible factor (HIF) prolyl hydroxylases (PHDs) are drug targets for the treatment of anaemia, while the procollagen prolyl hydroxylases and other 2-oxoglutarate dependent oxygenases are potential therapeutic targets for treatment of cancer, fibrotic disease, and infection. We describe assay development and inhibition studies for a procollagen prolyl hydroxylase from Paramecium bursaria chlorella virus 1 (vCPH). The results reveal HIF PHD inhibitors in clinical trials also inhibit vCPH. Implications for the targeting of the human PHDs and microbial prolyl hydroxylases are discussed.
真核生物脯氨酸残基的羟化在胶原蛋白生物合成和低氧信号中很重要。缺氧诱导因子 (HIF) 脯氨酰羟化酶 (PHD) 是治疗贫血的药物靶点,而原胶原蛋白脯氨酰羟化酶和其他 2-酮戊二酸依赖性加氧酶是治疗癌症、纤维化疾病和感染的潜在治疗靶点。我们描述了来自 Paramecium bursaria chlorella virus 1 (vCPH) 的原胶原蛋白脯氨酰羟化酶的测定开发和抑制研究。结果表明,临床试验中的 HIF PHD 抑制剂也抑制 vCPH。讨论了针对人 PHD 和微生物脯氨酰羟化酶的意义。