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细胞色素 P450 调节:血红素和脱辅基蛋白在合成、组装、修复和处理中的相互作用。

Cytochrome P450 regulation: the interplay between its heme and apoprotein moieties in synthesis, assembly, repair, and disposal.

机构信息

Department of Cellular and Molecular Pharmacology, The Liver Center, University of California, San Francisco, 94158, USA.

出版信息

Drug Metab Rev. 2011 Feb;43(1):1-26. doi: 10.3109/03602532.2010.515222. Epub 2010 Sep 23.

Abstract

Heme is vital to our aerobic universe. Heme cellular content is finely tuned through an exquisite control of synthesis and degradation. Heme deficiency is deleterious to cells, whereas excess heme is toxic. Most of the cellular heme serves as the prosthetic moiety of functionally diverse hemoproteins, including cytochromes P450 (P450s). In the liver, P450s are its major consumers, with >50% of hepatic heme committed to their synthesis. Prosthetic heme is the sine qua non of P450 catalytic biotransformation of both endo- and xenobiotics. This well-recognized functional role notwithstanding, heme also regulates P450 protein synthesis, assembly, repair, and disposal. These less well-appreciated aspects are reviewed herein.

摘要

血红素对我们的需氧生物至关重要。血红素细胞内含量通过精细调控合成和降解来实现。血红素缺乏对细胞有害,而过量的血红素则有毒。大多数细胞血红素作为功能多样的血红素蛋白(包括细胞色素 P450(P450s))的辅基。在肝脏中,P450s 是其主要的血红素消耗者,超过 50%的肝血红素用于它们的合成。辅基血红素是 P450 对内源和外源生物转化的必要条件。尽管这一公认的功能作用,但血红素也调节 P450 蛋白的合成、组装、修复和处理。本文回顾了这些不太为人所知的方面。

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