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首页> 外文期刊>Journal of cell biology >Kinetic Analysis of Secretory Protein Traffic and Characterization of Golgi to Plasma Membrane Transport Intermediates in Living Cells
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Kinetic Analysis of Secretory Protein Traffic and Characterization of Golgi to Plasma Membrane Transport Intermediates in Living Cells

机译:分泌蛋白运输的动力学分析和高尔基体到活细胞中血浆膜运输中间体的表征

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Quantitative time-lapse imaging data of single cells expressing the transmembrane protein, vesicular stomatitis virus ts045 G protein fused to green fluorescent protein (VSVG–GFP), were used for kinetic modeling of protein traffic through the various compartments of the secretory pathway. A series of first order rate laws was sufficient to accurately describe VSVG–GFP transport, and provided compartment residence times and rate constants for transport into and out of the Golgi complex and delivery to the plasma membrane. For ER to Golgi transport the mean rate constant (i.e., the fraction of VSVG–GFP moved per unit of time) was 2.8% per min, for Golgi to plasma membrane transport it was 3.0% per min, and for transport from the plasma membrane to a degradative site it was 0.25% per min. Because these rate constants did not change as the concentration of VSVG–GFP in different compartments went from high (early in the experiment) to low (late in the experiment), secretory transport machinery was never saturated during the experiments.The processes of budding, translocation, and fusion of post-Golgi transport intermediates carrying VSVG– GFP to the plasma membrane were also analyzed using quantitative imaging techniques. Large pleiomorphic tubular structures, rather than small vesicles, were found to be the primary vehicles for Golgi to plasma membrane transport of VSVG–GFP. These structures budded as entire domains from the Golgi complex and underwent dynamic shape changes as they moved along microtubule tracks to the cell periphery. They carried up to 10,000 VSVG–GFP molecules and had a mean life time in COS cells of 3.8 min. In addition, they fused with the plasma membrane without intersecting other membrane transport pathways in the cell. These properties suggest that the post-Golgi intermediates represent a unique transport organelle for conveying large quantities of protein cargo from the Golgi complex directly to the plasma membrane.
机译:表达跨膜蛋白,水泡性口炎病毒ts045 G蛋白与绿色荧光蛋白(VSVG-GFP)融合的单细胞的定量延时成像数据用于通过分泌途径各个区室进行蛋白运输的动力学模型。一系列一阶速率定律足以准确描述VSVG-GFP的运输,并提供了进入和离开高尔基复合体以及传递至质膜的隔室停留时间和速率常数。对于ER到高尔基体的运输,平均速率常数(即,每单位时间移动的VSVG-GFP的比例)为每分钟2.8%,对于高尔基体至质膜​​的运输,其平均速率为每分钟3.0%,对于从质膜的运输到降解位点为每分钟0.25%。由于这些速率常数不会随不同腔室中VSVG-GFP浓度从高(实验初期)到低(实验后期)的变化而变化,因此分泌转运机制在实验过程中从未饱和。还使用定量成像技术分析了携带VSVG–GFP的高尔基后转运中间体的转运和融合。发现大的多形管状结构而不是小囊泡是高尔基体向VSVG-GFP质膜转运的主要载体。这些结构作为高尔基复合体的整个结构域萌芽,并随着它们沿着微管轨道移动到细胞外围而发生动态形状变化。它们携带多达10,000个VSVG-GFP分子,在COS细胞中的平均寿命为3.8分钟。此外,它们与质膜融合而没有与细胞中的其他膜运输途径相交。这些性质表明,高尔基体后中间体代表了一种独特的运输细胞器,可将大量的蛋白质货物从高尔基体直接运输到质膜。

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