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A simple supported tubulated bilayer system for evaluating protein-mediated membrane remodeling

机译:一种简单的支撑的管道双层系统,用于评估蛋白质介导的膜重塑

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Fusion and fission of cellular membranes involve dramatic, protein-mediated changes in membrane curvature. Many of the experimental methods useful for investigating curvature sensing or generation require specialized equipment. We have developed a system based on supported lipid bilayers (SLBs) in which lipid tubules are simple to produce and several types of membrane remodeling events can be readily imaged using widely available instrumentation (e.g., tubule fission and/or membrane budding). Briefly, high ionic strength during lipid bilayer deposition results in incorporation of excess lipids in the SLB. After sequentially washing with water and physiological ionic strength buffer solutions, lipid tubules form spontaneously. We find that tubule formation results from solution-dependent spreading of the SLB; washing from water into physiological ionic strength buffer solution leads to expansion of the bilayer and formation of tubules. Conversely, washing from physiological buffer into water results in contraction of the membrane and loss of tubules. We demonstrate the utility of these supported tubulated bilayers, termed "STuBs," with an investigation of Sar1B, a small Ras family G-protein known to influence membrane curvature. The addition of Sar1B to STuBs results in dramatic changes in tubule topology and eventual tubule fission. Overall, STuBs are a simple experimental system, useful for monitoring protein-mediated effects on membrane topology in real time, under physiologically relevant conditions.
机译:细胞膜的融合和裂变涉及膜曲率的戏剧性,蛋白质介导的变化。许多用于研究曲率感测或一代的实验方法需要专门的设备。我们开发了一种基于支持的脂质双层(SLB)的系统,其中脂质小管易于产生,并且可以使用广泛可选的仪器(例如管裂解和/或膜芽面)容易地成像几种类型的膜重塑事件。简而言之,脂质双层沉积期间的高离子强度导致在SLB中掺入过量的脂质。用水和生理离子强度缓冲溶液依次洗涤后,脂质小管形成自发。我们发现小管形成由SLB的溶液依赖性扩散产生;从水中洗涤到生理离子强度缓冲溶液中,导致双层的膨胀和小管的形成。相反,从生理缓冲液中洗涤到水中导致膜的收缩和小管的损失。我们证明了这些支持的管道双层的效用,随着SAR1B的调查,称为影响膜曲率的小RAS系列G蛋白,称为“残留物”。将SAR1B添加到存根导致小管拓扑的剧烈变化和最终管状裂缝。总体而言,存根是一种简单的实验系统,可用于在生理相关条件下实时监测蛋白质介导对膜拓扑的影响。

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