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高尔基体内部运输的定量分析表明所有货物都存在小泡间交换。

Quantitative analysis of intra-Golgi transport shows intercisternal exchange for all cargo.

机构信息

Laboratoire Gulliver, Centre National de la Recherche Scientifique-Ecole Supérieure de Physique et de Chimie Industrielles, Unité Mixte de Recherche 7083, 75231 Paris Cedex 05, France.

出版信息

Proc Natl Acad Sci U S A. 2013 Sep 24;110(39):15692-7. doi: 10.1073/pnas.1303358110. Epub 2013 Sep 9.

Abstract

The mechanisms controlling the transport of proteins through the Golgi stack of mammalian and plant cells is the subject of intense debate, with two models, cisternal progression and intercisternal exchange, emerging as major contenders. A variety of transport experiments have claimed support for each of these models. We reevaluate these experiments using a single quantitative coarse-grained framework of intra-Golgi transport that accounts for both transport models and their many variants. Our analysis makes a definitive case for the existence of intercisternal exchange both for small membrane proteins and large protein complexes--this implies that membrane structures larger than the typical protein-coated vesicles must be involved in transport. Notwithstanding, we find that current observations on protein transport cannot rule out cisternal progression as contributing significantly to the transport process. To discriminate between the different models of intra-Golgi transport, we suggest experiments and an analysis based on our extended theoretical framework that compare the dynamics of transiting and resident proteins.

摘要

哺乳动物和植物细胞中控制蛋白质通过高尔基体堆叠运输的机制是激烈争论的主题,两个模型,即小泡进展和小泡间交换,作为主要竞争者出现。各种运输实验声称支持这两种模型中的每一种。我们使用一个单一的定量粗粒化的高尔基体内部运输框架来重新评估这些实验,该框架既考虑了运输模型及其许多变体。我们的分析明确证明了小膜蛋白和大蛋白复合物之间存在小泡间交换——这意味着运输过程中必须涉及比典型的蛋白包被小泡更大的膜结构。尽管如此,我们发现,关于蛋白质运输的当前观察结果并不能排除小泡进展对运输过程有重要贡献。为了区分高尔基体内部运输的不同模型,我们建议根据我们扩展的理论框架进行实验和分析,比较过境蛋白和驻留蛋白的动力学。

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