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缺氧诱导因子羟化酶的生物化学。

Biochemistry of the hypoxia-inducible factor hydroxylases.

机构信息

Chemistry Research Laboratory, Department of Chemistry and the Ineos Oxford Institute for Antimicrobial Research, 12 Mansfield Road, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, United Kingdom.

Chemistry Research Laboratory, Department of Chemistry and the Ineos Oxford Institute for Antimicrobial Research, 12 Mansfield Road, Department of Chemistry, University of Oxford, Oxford, OX1 3TA, United Kingdom.

出版信息

Curr Opin Chem Biol. 2024 Apr;79:102428. doi: 10.1016/j.cbpa.2024.102428. Epub 2024 Feb 7.

Abstract

The hypoxia-inducible factors are α,β-heterodimeric transcription factors that mediate the chronic response to hypoxia in humans and other animals. Protein hydroxylases belonging to two different structural subfamilies of the Fe(II) and 2-oxoglutarate (2OG)-dependent oxygenase superfamily modify HIFα. HIFα prolyl-hydroxylation, as catalysed by the PHDs, regulates HIFα levels and, consequently, α,β-HIF levels. HIFα asparaginyl-hydroxylation, as catalysed by factor inhibiting HIF (FIH), regulates the transcriptional activity of α,β-HIF. The activities of the PHDs and FIH are regulated by O availability, enabling them to act as hypoxia sensors. We provide an overview of the biochemistry of the HIF hydroxylases, discussing evidence that their kinetic and structural properties may be tuned to their roles in the HIF system. Avenues for future research and therapeutic modulation are discussed.

摘要

缺氧诱导因子是 α、β-异二聚体转录因子,介导人类和其他动物对缺氧的慢性反应。属于铁(II)和 2-氧戊二酸(2OG)依赖性氧合酶超家族的两种不同结构亚家族的蛋白羟化酶修饰 HIFα。PHD 催化的 HIFα脯氨酰羟化作用调节 HIFα水平,进而调节 α、β-HIF 水平。FIH 催化的 HIFα天冬酰胺羟化作用调节 α、β-HIF 的转录活性。PHD 和 FIH 的活性受 O 可用性的调节,使它们能够作为缺氧传感器发挥作用。我们提供了 HIF 羟化酶的生物化学概述,讨论了它们的动力学和结构特性可能被调整到它们在 HIF 系统中的作用的证据。还讨论了未来研究和治疗调节的途径。

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