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肯尼迪途径——从头合成磷脂酰乙醇胺和磷脂酰胆碱。

The Kennedy pathway--De novo synthesis of phosphatidylethanolamine and phosphatidylcholine.

机构信息

Centre for Biomolecular Sciences, University of St. Andrews, North Haugh, St. Andrews, Fife, Scotland, UK.

出版信息

IUBMB Life. 2010 Jun;62(6):414-28. doi: 10.1002/iub.337.

Abstract

The glycerophospholipids phosphatidylcholine (PC) and phosphatidylethanolamine (PE) account for greater than 50% of the total phospholipid species in eukaryotic membranes and thus play major roles in the structure and function of those membranes. In most eukaryotic cells, PC and PE are synthesized by an aminoalcoholphosphotransferase reaction, which uses sn-1,2-diradylglycerol and either CDP-choline or CDP-ethanolamine, respectively. This is the last step in a biosynthetic pathway known as the Kennedy pathway, so named after Eugene Kennedy who elucidated it over 50 years ago. This review will cover various aspects of the Kennedy pathway including: each of the biosynthetic steps, the functions and roles of the phospholipid products PC and PE, and how the Kennedy pathway has the potential of being a chemotherapeutic target against cancer and various infectious diseases.

摘要

甘油磷脂酰胆碱 (PC) 和磷脂酰乙醇胺 (PE) 占真核细胞膜中总磷脂种类的 50%以上,因此在这些膜的结构和功能中发挥主要作用。在大多数真核细胞中,PC 和 PE 是通过氨基醇磷酸转移酶反应合成的,该反应分别使用 sn-1,2-二脂酰甘油和 CDP-胆碱或 CDP-乙醇胺。这是一种称为肯尼通路的生物合成途径的最后一步,之所以这样命名是因为 Eugene Kennedy 五十多年前阐明了这一途径。本综述将涵盖肯尼通路的各个方面,包括:每个生物合成步骤、磷脂产物 PC 和 PE 的功能和作用,以及肯尼通路如何有可能成为抗癌和各种传染病的化疗靶点。

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