包膜硬化解释了凝集素介导的内吞共识途径

Felix FreyIST Austria, Ulrich S. SchwarzHeidelberg University
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引用次数: 0

摘要

凝集素介导的内吞是真核细胞摄取细胞外物质的主要途径,但驱动这一过程的主要物理机制仍然难以捉摸。最近有几种高分辨率成像技术被用于不同的细胞系,以测量clathrin包被坑在整个生命周期中的几何特性。在这里,我们首先展示了所有数据集都遵循相同的共识路径,这一点在最近引入的合作曲率模型中得到了很好的描述,该模型预测了在有限面积上从平坦到弯曲的转变,随后是线性增长和随后的曲率饱和。然后,我们将质膜和凝集素外膜复合体的能量模型应用于共识途径,结果表明,内陷的主要机制是外膜变硬,这源于不同凝集素分子之间的合作性相互作用,并逐步推动系统走向其固有曲率。我们的理论预测有两个长度尺度决定了内陷的时间过程,即发生从平坦到弯曲转变的斑块大小和最终凹坑半径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Coat stiffening explains the consensus pathway of clathrin-mediated endocytosis
Clathrin-mediated endocytosis is the main pathway used by eukaryotic cells to take up extracellular material, but the dominant physical mechanisms driving this process are still elusive. Recently several high-resolution imaging techniques have been used on different cell lines to measure the geometrical properties of clathrin-coated pits over their whole lifetime. Here we first show that all datasets follow the same consensus pathway, which is well described by the recently introduced cooperative curvature model, which predicts a flat-to curved transition at finite area, followed by linear growth and subsequent saturation of curvature. We then apply an energetic model for the composite of plasma membrane and clathrin coat to the consensus pathway to show that the dominant mechanism for invagination is coat stiffening, which results from cooperative interactions between the different clathrin molecules and progressively drives the system towards its intrinsic curvature. Our theory predicts that two length scales determine the time course of invagination, namely the patch size at which the flat-to-curved transition occurs and the final pit radius.
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