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诱导表达跨膜蛋白在趋磁细菌AMB-1 上的细菌磁性颗粒。

Inducible expression of transmembrane proteins on bacterial magnetic particles in Magnetospirillum magneticum AMB-1.

机构信息

Department of Biotechnology, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo 184-8588, Japan.

出版信息

Appl Environ Microbiol. 2010 Feb;76(4):1152-7. doi: 10.1128/AEM.01755-09. Epub 2009 Dec 28.

Abstract

Bacterial magnetic particles (BacMPs) produced by the magnetotactic bacterium Magnetospirillum magneticum AMB-1 are used for a variety of biomedical applications. In particular, the lipid bilayer surrounding BacMPs has been reported to be amenable to the insertion of recombinant transmembrane proteins; however, the display of transmembrane proteins in BacMP membranes remains a technical challenge due to the cytotoxic effects of the proteins when they are overexpressed in bacterial cells. In this study, a tetracycline-inducible expression system was developed to display transmembrane proteins on BacMPs. The expression and localization of the target proteins were confirmed using luciferase and green fluorescent protein as reporter proteins. Gene expression was suppressed in the absence of anhydrotetracycline, and the level of protein expression could be controlled by modulating the concentration of the inducer molecule. This system was implemented to obtain the expression of the tetraspanin CD81. The truncated form of CD81 including the ligand binding site was successfully displayed at the surface of BacMPs by using Mms13 as an anchor protein and was shown to bind the hepatitis C virus envelope protein E2. These results suggest that the tetracycline-inducible expression system described here will be a useful tool for the expression and display of transmembrane proteins in the membranes of BacMPs.

摘要

由趋磁细菌 Magnetospirillum magneticum AMB-1 产生的细菌磁性颗粒 (BacMPs) 被用于各种生物医学应用。特别是,已经报道了 BacMPs 周围的脂质双层可插入重组跨膜蛋白;然而,由于在细菌细胞中过表达时蛋白质的细胞毒性作用,跨膜蛋白在 BacMP 膜中的显示仍然是一个技术挑战。在这项研究中,开发了一种四环素诱导表达系统,用于在 BacMPs 上展示跨膜蛋白。使用荧光素酶和绿色荧光蛋白作为报告蛋白来确认目标蛋白的表达和定位。在没有脱水四环素的情况下抑制基因表达,并且可以通过调节诱导剂分子的浓度来控制蛋白质表达水平。该系统用于获得 tetraspanin CD81 的表达。通过使用 Mms13 作为锚定蛋白,成功地将包括配体结合位点的 CD81 的截断形式展示在 BacMPs 的表面上,并显示出与丙型肝炎病毒包膜蛋白 E2 的结合。这些结果表明,这里描述的四环素诱导表达系统将成为在 BacMPs 膜中表达和展示跨膜蛋白的有用工具。

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