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由Lol回避信号导致的大肠杆菌脂蛋白内膜滞留的潜在机制。

Mechanism underlying the inner membrane retention of Escherichia coli lipoproteins caused by Lol avoidance signals.

作者信息

Hara Takashi, Matsuyama Shin-ichi, Tokuda Hajime

机构信息

Institute of Molecular and Cellular Biosciences, University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan.

出版信息

J Biol Chem. 2003 Oct 10;278(41):40408-14. doi: 10.1074/jbc.M307836200. Epub 2003 Aug 1.

Abstract

Escherichia coli lipoproteins are localized to either the inner or outer membrane depending on the residue at position 2. The inner membrane retention signal, Asp at position 2 in combination with certain residues at position 3, functions as a Lol avoidance signal, i.e. the signal inhibits the recognition of lipoproteins by LolCDE that releases lipoproteins from the inner membrane. To understand the role of the residue at position 2, outer membrane-specific lipoproteins with Cys at position 2 were subjected to chemical modification followed by the release reaction in reconstituted proteoliposomes. Sulfhydryl-specific introduction of nonprotein molecules or a negative charge to Cys did not inhibit the LolCDE-dependent release. In contrast, oxidation of Cys to cysteic acid resulted in generation of the Lol avoidance signal, indicating that the Lol avoidance signal requires a critical length of negative charge at the second residue. Furthermore, not only modification of the carboxylic acid of Asp at position 2 but also that of the amine of phosphatidylethanolamine abolished the Lol avoidance function. Based on these results, the Lol avoidance mechanism is discussed.

摘要

大肠杆菌脂蛋白根据第2位的残基定位于内膜或外膜。内膜保留信号,即第2位的天冬氨酸与第3位的某些残基结合,作为一种Lol回避信号,也就是说,该信号抑制LolCDE对脂蛋白的识别,而LolCDE会将脂蛋白从内膜释放出来。为了了解第2位残基的作用,对第2位为半胱氨酸的外膜特异性脂蛋白进行化学修饰,然后在重组蛋白脂质体中进行释放反应。对半胱氨酸进行巯基特异性引入非蛋白质分子或负电荷并不抑制LolCDE依赖性释放。相反,半胱氨酸氧化成半胱磺酸导致Lol回避信号的产生,表明Lol回避信号需要第2位残基有一定长度的负电荷。此外,不仅对第2位天冬氨酸的羧酸进行修饰,而且对磷脂酰乙醇胺的胺进行修饰也消除了Lol回避功能。基于这些结果,对Lol回避机制进行了讨论。

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