Liese Susanne, Carlson Andreas
Department of Mathematics, Mechanics Division, University of Oslo, Oslo, Norway.
Biophys J. 2021 Jun 15;120(12):2482-2489. doi: 10.1016/j.bpj.2021.04.029. Epub 2021 May 21.
The steric repulsion between proteins on biological membranes is one of the most generic mechanisms that cause membrane shape changes. We present a minimal model in which a spontaneous curvature is induced by asymmetric protein crowding. Our results show that the interplay between the induced spontaneous curvature and the membrane tension determines the energy-minimizing shapes, which describes the wide range of experimentally observed membrane shapes, i.e., flat membranes, spherical vesicles, elongated tubular protrusions, and pearling structures. Moreover, the model gives precise predictions on how membrane shape changes by protein crowding can be tuned by controlling the protein size, the density of proteins, and the size of the crowded domain.
生物膜上蛋白质之间的空间排斥是导致膜形状变化的最普遍机制之一。我们提出了一个最小模型,其中不对称的蛋白质聚集诱导了自发曲率。我们的结果表明,诱导的自发曲率与膜张力之间的相互作用决定了能量最小化的形状,这描述了实验中观察到的广泛的膜形状,即平膜、球形囊泡、细长的管状突起和串珠状结构。此外,该模型还对如何通过控制蛋白质大小、蛋白质密度和聚集域大小来调节蛋白质聚集引起的膜形状变化给出了精确预测。