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利用沙氏利什曼原虫无细胞提取物合成人类溶质载体。

Exploiting Leishmania tarentolae cell-free extracts for the synthesis of human solute carriers.

作者信息

Ruehrer Suzan, Michel Hartmut

机构信息

Department of Molecular Membrane Biology, Max Planck Institute of Biophysics, Frankfurt am Main, Germany.

出版信息

Mol Membr Biol. 2013 Jul;30(4):288-302. doi: 10.3109/09687688.2013.807362. Epub 2013 Jun 26.

Abstract

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.

摘要

无细胞蛋白质合成提供了一种多功能的替代方案,以补充体内表达系统。然而,原核无细胞系统的使用常常导致蛋白质无功能。我们对先前设计的基于原虫杜氏利什曼原虫(摩尔壁虎的一种寄生虫)的无细胞系统进行了改进,并结合了一种基于物种独立翻译序列的质粒,以便在2小时的反应时间内生产人类膜蛋白。我们成功地建立了以人类有机阴离子转运体SLC17A3作为模型膜蛋白的无细胞合成膜蛋白的所有四种常用表达模式:(i)不添加任何疏水环境时以沉淀形式存在,(ii)在去污剂存在的情况下,(iii)添加脂质体,以及(iv)补充纳米圆盘。我们利用这个改进后的系统从20个不同家族中合成了22种人类溶质载体。我们的结果证明了杜氏利什曼原虫无细胞系统在沉淀模式下生产多种人类溶质载体的能力。此外,纯化后的SLC17A3显示出寡聚状态的形成。

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