Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstr 108, 01307 Dresden, Germany.
Proc Natl Acad Sci U S A. 2009 Dec 29;106(52):22245-50. doi: 10.1073/pnas.0907354106. Epub 2009 Dec 23.
In biological processes, such as fission, fusion and trafficking, it has been shown that lipids of different shapes are sorted into regions with different membrane curvatures. This lipid sorting has been hypothesized to be due to the coupling between the membrane curvature and the lipid's spontaneous curvature, which is related to the lipid's molecular shape. On the other hand, theoretical predictions and simulations suggest that the curvature preference of lipids, due to shape alone, is weaker than that observed in biological processes. To distinguish between these different views, we have directly measured the curvature preferences of several lipids by using a fluorescence-based method. We prepared small unilamellar vesicles of different sizes with a mixture of egg-PC and a small mole fraction of N-nitrobenzoxadiazole (NBD)-labeled phospholipids or lysophospholipids of different chain lengths and saturation, and measured the NBD equilibrium distribution across the bilayer. We observed that the transverse lipid distributions depended linearly on membrane curvature, allowing us to measure the curvature coupling coefficient. Our measurements are in quantitative agreement with predictions based on earlier measurements of the spontaneous curvatures of the corresponding nonfluorescent lipids using X-ray diffraction. We show that, though some lipids have high spontaneous curvatures, they nevertheless showed weak curvature preferences because of the low values of the lipid molecular areas. The weak curvature preference implies that the asymmetric lipid distributions found in biological membranes are not likely to be driven by the spontaneous curvature of the lipids, nor are lipids discriminating sensors of membrane curvature.
在生物过程中,如裂变、融合和运输,已经表明不同形状的脂质被分拣到具有不同膜曲率的区域。这种脂质分拣被假设是由于膜曲率和脂质的自发曲率之间的耦合,这与脂质的分子形状有关。另一方面,理论预测和模拟表明,由于形状单一,脂质的曲率偏好比在生物过程中观察到的要弱。为了区分这些不同的观点,我们通过使用基于荧光的方法直接测量了几种脂质的曲率偏好。我们用鸡蛋-PC 和一小部分 N-硝基苯并恶二唑(NBD)标记的磷脂或不同链长和饱和度的溶血磷脂的混合物制备了不同大小的小单层囊泡,并测量了 NBD 在双层中的平衡分布。我们观察到横向脂质分布与膜曲率呈线性关系,这使我们能够测量曲率耦合系数。我们的测量结果与基于早期使用 X 射线衍射测量相应非荧光脂质的自发曲率的预测定量一致。我们表明,尽管一些脂质具有高自发曲率,但由于脂质分子面积较低,它们仍然表现出较弱的曲率偏好。弱曲率偏好意味着在生物膜中发现的不对称脂质分布不太可能是由脂质的自发曲率驱动的,脂质也不是膜曲率的敏感传感器。