论文标题
蛋白质介导的管的形成由快速过渡控制
Formation of protein-mediated tubes is governed by a snapthrough transition
论文作者
论文摘要
质膜管在细胞膜和细胞内细胞器的膜中无处不在。他们在贩运,离子运输和细胞运动中起着至关重要的作用。质膜管的形成可能是由于作用在膜上的局部力或由膜结合蛋白引起的曲率。在这里,我们提出了一个数学框架,以模拟由诱导各向异性自发曲率的蛋白质形成的圆柱形管状突起。我们的分析表明,管半径取决于有效的张力,其中包括裸露膜张力和蛋白质诱导的曲率的贡献。我们还发现,管的长度从短的圆顶形膜到长圆柱体发生突然过渡,并且这种过渡是快速不稳定的特征。最后,我们表明,快速不稳定性取决于不同的参数,包括外套面积,弯曲模量以及蛋白质诱导的曲率的程度。我们的发现在诸如内吞作用,肌细胞中的T型管形成和线粒体中的Cristae形成等过程中,由于条膜蛋白在诸如棒状域的蛋白质中具有影响。
Plasma membrane tubes are ubiquitous in cellular membranes and in the membranes of intracellular organelles. They play crucial roles in trafficking, ion transport, and cellular motility. The formation of plasma membrane tubes can be due to localized forces acting on the membrane or by curvature-induced by membrane-bound proteins. Here, we present a mathematical framework to model cylindrical tubular protrusions formed by proteins that induce anisotropic spontaneous curvature. Our analysis revealed that the tube radius depends on an effective tension that includes contributions from the bare membrane tension and the protein-induced curvature. We also found that the length of the tube undergoes an abrupt transition from a short, dome-shaped membrane to a long cylinder and this transition is characteristic of a snapthrough instability. Finally, we show that the snapthrough instability depends on the different parameters including coat area, bending modulus, and extent of protein-induced curvature. Our findings have implications for tube formation due to BAR-domain proteins in processes such as endocytosis, t-tubule formation in myocytes, and cristae formation in mitochondria.