利用利什曼原虫无细胞提取物合成人溶质载体。

Q3 Biochemistry, Genetics and Molecular Biology Molecular Membrane Biology Pub Date : 2013-07-01 Epub Date: 2013-06-26 DOI:10.3109/09687688.2013.807362
Suzan Ruehrer, Hartmut Michel
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引用次数: 10

摘要

无细胞蛋白生产提供了补充体内表达系统的多功能替代方案。然而,使用原核无细胞系统通常会导致无功能蛋白质。我们修改了先前设计的无细胞系统,该系统基于摩尔壁虎的一种寄生虫利什曼绦虫(tarentolae),以及基于种独立翻译序列的质粒,在2小时的反应时间内产生人膜蛋白。我们成功建立了四种常用的无细胞合成膜蛋白的表达模式,以人类有机阴离子转运体SLC17A3为模型膜蛋白:(i)在没有添加任何疏水环境的情况下作为沉淀,(ii)在洗涤剂存在的情况下,(iii)添加脂质体,(iv)添加纳米片。利用该系统合成了来自20个不同家族的22种人类溶质载体。我们的结果证明了利什曼原虫无细胞系统在沉淀模式下生产大量人类溶质载体的能力。此外,纯化的SLC17A3显示出低聚态的形成。
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Exploiting Leishmania tarentolae cell-free extracts for the synthesis of human solute carriers.

Cell-free protein production offers a versatile alternative to complement in vivo expression systems. However, usage of prokaryotic cell-free systems often leads to non-functional proteins. We modified a previously designed cell-free system based on the protozoan Leishmania tarentolae, a parasite of the Moorish gecko Tarentola mauritanica, together with a species-independent translational sequences-based plasmid to produce human membrane proteins in 2 hours reaction time. We successfully established all four commonly used expression modes for cell-free synthesis of membrane proteins with a human organic anion transporter, SLC17A3, as a model membrane protein: (i) As precipitates without the addition of any hydrophobic environment, (ii) in the presence of detergents, (iii) with the addition of liposomes, and (iv) supplemented with nanodiscs. We utilized this adapted system to synthesize 22 human solute carriers from 20 different families. Our results demonstrate the capability of the Leishmania tarentolae cell-free system for the production of a huge variety of human solute carriers in the precipitate mode. Furthermore, purified SLC17A3 shows the formation of an oligomeric state.

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来源期刊
Molecular Membrane Biology
Molecular Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Cessation. Molecular Membrane Biology provides a forum for high quality research that serves to advance knowledge in molecular aspects of biological membrane structure and function. The journal welcomes submissions of original research papers and reviews in the following areas: • Membrane receptors and signalling • Membrane transporters, pores and channels • Synthesis and structure of membrane proteins • Membrane translocation and targeting • Lipid organisation and asymmetry • Model membranes • Membrane trafficking • Cytoskeletal and extracellular membrane interactions • Cell adhesion and intercellular interactions • Molecular dynamics and molecular modelling of membranes. • Antimicrobial peptides.
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