Collins Marcus D, Keller Sarah L
Department of Chemistry, University of Washington, Seattle, WA 98195-1700, USA.
Proc Natl Acad Sci U S A. 2008 Jan 8;105(1):124-8. doi: 10.1073/pnas.0702970105. Epub 2008 Jan 2.
Plasma membranes of cells are asymmetric in both lipid and protein composition. The mechanism by which proteins on both sides of the membrane colocalize during signaling events is unknown but may be due to the induction of inner leaflet domains by the outer leaflet. Here we show that liquid domains form in asymmetric Montal-Mueller planar bilayers in which one leaflet's composition would phase-separate in a symmetric bilayer and the other's would not. Equally important, by tuning the lipid composition of the second leaflet, we are able to suppress domains in the first leaflet. When domains are present in asymmetric membranes, each leaflet contains regions of three distinct lipid compositions, implying strong interleaflet interactions. Our results show that mechanisms of domain induction between the outer and inner leaflets of cell plasma membranes do not necessarily require the participation of membrane proteins. Based on these findings, we suggest mechanisms by which cells could actively regulate protein function by modulating local lipid composition or interleaflet interactions.
细胞的质膜在脂质和蛋白质组成上都是不对称的。在信号传导过程中,膜两侧的蛋白质共定位的机制尚不清楚,但可能是由于外小叶对内小叶结构域的诱导作用。在这里,我们展示了在不对称的蒙塔尔-米勒平面双层膜中形成的液相结构域,其中一个小叶的组成在对称双层膜中会发生相分离,而另一个则不会。同样重要的是,通过调节第二个小叶的脂质组成,我们能够抑制第一个小叶中的结构域。当不对称膜中存在结构域时,每个小叶都包含具有三种不同脂质组成的区域,这意味着小叶间存在强烈的相互作用。我们的结果表明,细胞质膜外小叶和内小叶之间的结构域诱导机制不一定需要膜蛋白的参与。基于这些发现,我们提出了细胞可以通过调节局部脂质组成或小叶间相互作用来主动调节蛋白质功能的机制。