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用于整合通过无细胞表达合成的膜内在蛋白的金表面拴系脂质双层的制备。

Preparation of tethered-lipid bilayers on gold surfaces for the incorporation of integral membrane proteins synthesized by cell-free expression.

作者信息

Coutable Angélique, Thibault Christophe, Chalmeau Jérôme, François Jean Marie, Vieu Christophe, Noireaux Vincent, Trévisiol Emmanuelle

机构信息

Université de Toulouse , INSA, UPS, INP, LISBP, 135 Avenue de Rangueil, F-31077 Toulouse, France.

出版信息

Langmuir. 2014 Mar 25;30(11):3132-41. doi: 10.1021/la5004758. Epub 2014 Mar 11.

Abstract

There is an increasing interest to express and study membrane proteins in vitro. New techniques to produce and insert functional membrane proteins into planar lipid bilayers have to be developed. In this work, we produce a tethered lipid bilayer membrane (tBLM) to provide sufficient space for the incorporation of the integral membrane protein (IMP) Aquaporin Z (AqpZ) between the tBLM and the surface of the sensor. We use a gold (Au)-coated sensor surface compatible with mechanical sensing using a quartz crystal microbalance with dissipation monitoring (QCM-D) or optical sensing using the surface plasmon resonance (SPR) method. tBLM is produced by vesicle fusion onto a thin gold film, using phospholipid-polyethylene glycol (PEG) as a spacer. Lipid vesicles are composed of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-poly(ethyleneglycol)-2000-N-[3-(2-pyridyldithio)propionate], so-called DSPE-PEG-PDP, at different molar ratios (respectively, 99.5/0.5, 97.5/2.5, and 95/5 mol %), and tBLM formation is characterized using QCM-D, SPR, and atomic force technology (AFM). We demonstrate that tBLM can be produced on the gold surface after rupture of the vesicles using an α helical (AH) peptide, derived from hepatitis C virus NS5A protein, to assist the fusion process. A cell-free expression system producing the E. coli integral membrane protein Aquaporin Z (AqpZ) is directly incubated onto the tBLMs for expression and insertion of the IMP at the upper side of tBLMs. The incorporation of AqpZ into bilayers is monitored by QCM-D and compared to a control experiment (without plasmid in the cell-free expression system). We demonstrate that an IMP such as AqpZ, produced by a cell-free expression system without any protein purification, can be incorporated into an engineered tBLM preassembled at the surface of a gold-coated sensor.

摘要

体外表达和研究膜蛋白的兴趣与日俱增。必须开发新的技术来生产功能性膜蛋白并将其插入平面脂质双层中。在这项工作中,我们制备了一种拴系脂质双层膜(tBLM),以便在tBLM与传感器表面之间为整合膜蛋白(IMP)水通道蛋白Z(AqpZ)的掺入提供足够的空间。我们使用与机械传感兼容的金(Au)涂层传感器表面,该传感可通过带耗散监测的石英晶体微天平(QCM-D)进行,也可通过表面等离子体共振(SPR)方法进行光学传感。tBLM是通过囊泡融合到薄金膜上制备的,使用磷脂-聚乙二醇(PEG)作为间隔物。脂质囊泡由1-棕榈酰-2-油酰-sn-甘油-3-磷酸胆碱(POPC)和1,2-二硬脂酰-sn-甘油-3-磷酸乙醇胺-N-聚(乙二醇)-2000-N-[3-(2-吡啶二硫基)丙酸酯](即所谓的DSPE-PEG-PDP)以不同摩尔比(分别为99.5/0.5、97.5/2.5和95/5 mol%)组成,并且使用QCM-D、SPR和原子力技术(AFM)对tBLM的形成进行表征。我们证明,使用源自丙型肝炎病毒NS5A蛋白的α螺旋(AH)肽协助融合过程后,囊泡破裂后可在金表面制备tBLM。将产生大肠杆菌整合膜蛋白水通道蛋白Z(AqpZ)的无细胞表达系统直接孵育到tBLM上,以便在tBLM的上侧表达和插入IMP。通过QCM-D监测AqpZ掺入双层的情况,并与对照实验(无细胞表达系统中无质粒)进行比较。我们证明,由无任何蛋白质纯化的无细胞表达系统产生的IMP(如AqpZ)可掺入预先组装在金涂层传感器表面的工程化tBLM中。

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