Department of Physics, Cornell University, Ithaca, New York, USA.
Biophys J. 2011 Apr 6;100(7):1668-77. doi: 10.1016/j.bpj.2011.02.029.
We present a minimal model of plasma membrane heterogeneity that combines criticality with connectivity to cortical cytoskeleton. The development of this model was motivated by recent observations of micron-sized critical fluctuations in plasma membrane vesicles that are detached from their cortical cytoskeleton. We incorporate criticality using a conserved order parameter Ising model coupled to a simple actin cytoskeleton interacting through point-like pinning sites. Using this minimal model, we recapitulate several experimental observations of plasma membrane raft heterogeneity. Small (r ∼ 20 nm) and dynamic fluctuations at physiological temperatures arise from criticality. Including connectivity to the cortical cytoskeleton disrupts large fluctuations, prevents macroscopic phase separation at low temperatures (T ≤ 22°C), and provides a template for long-lived fluctuations at physiological temperature (T = 37°C). Cytoskeleton-stabilized fluctuations produce significant barriers to the diffusion of some membrane components in a manner that is weakly dependent on the number of pinning sites and strongly dependent on criticality. More generally, we demonstrate that critical fluctuations provide a physical mechanism for organizing and spatially segregating membrane components by providing channels for interaction over large distances.
我们提出了一个将临界性与皮质细胞骨架连接相结合的细胞膜异质性最小模型。该模型的发展源于最近观察到的从皮质细胞骨架上脱离的微尺度临界膜泡的波动。我们使用一个保守的伊辛模型作为临界点参数,该模型与通过点状钉扎位点相互作用的简单肌动蛋白细胞骨架耦合。通过这个最小模型,我们再现了细胞膜筏异质性的几个实验观察结果。生理温度下的小(r∼20nm)和动态波动来自临界点。与皮质细胞骨架的连接会破坏大的波动,防止在低温(T≤22°C)下发生宏观相分离,并为生理温度(T=37°C)下的长寿命波动提供模板。细胞骨架稳定的波动会对某些膜成分的扩散产生显著的阻碍,这种阻碍的方式与钉扎点的数量弱相关,而与临界性强相关。更一般地说,我们证明了临界波动通过提供远距离相互作用的通道,为组织和空间分隔膜成分提供了一种物理机制。