Suppr超能文献

ABC 转运蛋白与脂质的多样关系:概述。

Diverse relations between ABC transporters and lipids: An overview.

机构信息

Institute of Pharmacy and Biochemistry, Johannes Gutenberg University Mainz, Johann-Joachim-Becher-Weg 30, 55128 Mainz, Germany.

Institute of Pharmacy and Biochemistry, Johannes Gutenberg University Mainz, Johann-Joachim-Becher-Weg 30, 55128 Mainz, Germany.

出版信息

Biochim Biophys Acta Biomembr. 2017 Apr;1859(4):605-618. doi: 10.1016/j.bbamem.2016.09.023. Epub 2016 Sep 29.

Abstract

It was first discovered in 1992 that P-glycoprotein (Pgp, ABCB1), an ATP binding cassette (ABC) transporter, can transport phospholipids such as phosphatidylcholine, -ethanolamine and -serine as well as glucosylceramide and glycosphingolipids. Subsequently, many other ABC transporters were identified to act as lipid transporters. For substrate transport by ABC transporters, typically a classic, alternating access model with an ATP-dependent conformational switch between a high and a low affinity substrate binding site is evoked. Transport of small hydrophilic substrates can easily be imagined this way, as the molecule can in principle enter and exit the transporter in the same orientation. Lipids on the other hand need to undergo a 180° degree turn as they translocate from one membrane leaflet to the other. Lipids and lipidated molecules are highly diverse, so there may be various ways how to achieve their flipping and flopping. Nonetheless, an increase in biophysical, biochemical and structural data is beginning to shed some light on specific aspects of lipid transport by ABC transporters. In addition, there is now abundant evidence that lipids affect ABC transporter conformation, dynamics as well as transport and ATPase activity in general. In this review, we will discuss different ways in which lipids and ABC transporters interact and how lipid translocation may be achieved with a focus on the techniques used to investigate these processes. This article is part of a Special Issue entitled: Lipid order/lipid defects and lipid-control of protein activity edited by Dirk Schneider.

摘要

1992 年首次发现,P 糖蛋白(Pgp,ABCB1)是一种 ATP 结合盒(ABC)转运体,可转运磷脂,如卵磷脂、-乙醇胺和 -丝氨酸,以及葡萄糖神经酰胺和糖脂。随后,许多其他 ABC 转运体被鉴定为脂质转运体。对于 ABC 转运体的底物转运,通常会引发一种经典的交替访问模型,该模型具有一个依赖 ATP 的构象开关,在高亲和力和低亲和力底物结合位点之间进行切换。可以通过这种方式轻松想象小分子亲水性底物的转运,因为原则上分子可以以相同的方向进入和离开转运体。另一方面,脂质在从一个膜叶层转移到另一个膜叶层时需要经历 180°的翻转。脂质和脂质化分子高度多样化,因此可能有多种方法可以实现它们的翻转。尽管如此,越来越多的生物物理、生化和结构数据开始揭示 ABC 转运体转运脂质的特定方面。此外,现在有大量证据表明,脂质会影响 ABC 转运体的构象、动力学以及转运和 ATP 酶活性。在这篇综述中,我们将讨论脂质和 ABC 转运体相互作用的不同方式,以及如何实现脂质的易位,重点介绍用于研究这些过程的技术。本文是由 Dirk Schneider 编辑的题为“脂质有序/脂质缺陷和脂质控制蛋白活性”的特刊的一部分。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验