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脂筏内外不同形式的周围神经系统髓磷脂P0蛋白。

The different forms of PNS myelin P0 protein within and outside lipid rafts.

作者信息

Fasano Anna, Amoresano Angela, Rossano Rocco, Carlone Giulia, Carpentieri Andrea, Liuzzi Grazia Maria, Pucci Piero, Riccio Paolo

机构信息

Dipartimento di Biochimica e Biologia Molecolare "Ernesto Quagliariello", University of Bari, Bari, Italy.

出版信息

J Neurochem. 2008 Oct;107(1):291-301. doi: 10.1111/j.1471-4159.2008.05598.x. Epub 2008 Aug 1.

DOI:10.1111/j.1471-4159.2008.05598.x
PMID:18680558
Abstract

It is now well established that plasma membranes, such as the myelin sheath, are made of different microdomains with different lipid and protein composition. Lipid rafts are made mainly of sphingolipids and cholesterol, whereas the non-raft regions are made mainly of phosphoglycerides. Most myelin proteins may distribute themselves in raft and non-raft microdomains but the driving force that gives rise to their different distribution is not known yet. In this paper, we have studied the distribution of protein zero (P0), the most representative protein of PNS myelin, in the membrane microdomains. To this end, we have purified P0 from both non-raft (soluble P0, P0-S) and raft (P0-R) regions of PNS. Purified proteins were analyzed by two-dimensional gel electrophoresis and identified and characterized by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. A detailed structural description of the two P0 forms is given in terms of amino acid sequence, post-translational modifications, and composition of associated lipids. Our findings suggest that structural differences between the two proteins, mainly related to the glycogroups, might be responsible for their different localization.

摘要

现在已经充分证实,诸如髓鞘之类的质膜是由具有不同脂质和蛋白质组成的不同微区构成的。脂筏主要由鞘脂和胆固醇组成,而非脂筏区域主要由磷酸甘油酯组成。大多数髓鞘蛋白可能分布在脂筏和非脂筏微区中,但导致它们不同分布的驱动力尚不清楚。在本文中,我们研究了周围神经系统(PNS)髓鞘最具代表性的蛋白——零蛋白(P0)在膜微区中的分布。为此,我们从PNS的非脂筏(可溶性P0,P0-S)和脂筏(P0-R)区域中纯化了P0。通过二维凝胶电泳对纯化的蛋白进行分析,并通过基质辅助激光解吸/电离飞行时间质谱对其进行鉴定和表征。从氨基酸序列、翻译后修饰以及相关脂质组成方面对两种P0形式进行了详细的结构描述。我们的研究结果表明,这两种蛋白之间的结构差异,主要与糖基有关,可能是它们不同定位的原因。

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