Berger Mareike, Manghi Manoel, Destainville Nicolas
Laboratoire de Physique Théorique, IRSAMC, Université de Toulouse, CNRS, UPS, 118 route de Narbonne, F-31062 Toulouse, France.
J Phys Chem B. 2016 Oct 13;120(40):10588-10602. doi: 10.1021/acs.jpcb.6b07631. Epub 2016 Sep 30.
Cell membranes are out of thermodynamic equilibrium notably because of membrane recycling, i.e., active exchange of material with the cytosol. We propose an analytically tractable model of biomembrane predicting the effects of recycling on the size of protein nanodomains also called protein clusters. The model includes a short-range attraction between proteins and a weaker long-range repulsion which ensures the existence of so-called cluster phases in equilibrium, where monomeric proteins coexist with finite-size domains. Our main finding is that, when taking recycling into account, the typical cluster size at steady state increases logarithmically with the recycling rate at fixed protein concentration. Using physically realistic model parameters, the predicted 2-fold increase due to recycling in living cells is most likely experimentally measurable with the help of super-resolution microscopy.
细胞膜处于热力学非平衡状态,这主要是由于膜循环,即与细胞质进行物质的主动交换。我们提出了一个易于分析处理的生物膜模型,该模型可预测循环对蛋白质纳米结构域(也称为蛋白质簇)大小的影响。该模型包括蛋白质之间的短程吸引力和较弱的长程排斥力,这确保了平衡状态下所谓簇相的存在,即单体蛋白质与有限大小的结构域共存。我们的主要发现是,当考虑膜循环时,在固定蛋白质浓度下,稳态时典型的簇大小随循环速率呈对数增加。使用符合物理实际的模型参数,借助超分辨率显微镜,在活细胞中由于膜循环导致的2倍增加很可能在实验中被测量到。