Institute of Nanotechnology for Single Cell Analysis (INSCA), Beijing Advanced Innovation Center for Biomedical Engineering , Beihang University , Beijing 100191 , China.
State Key Laboratory of Medical Molecular Biology, School of Basic Medicine, Peking Union Medical College and Institute of Basic Medical Sciences , Chinese Academy of Medical Sciences , Beijing 100005 , China.
J Am Chem Soc. 2019 Oct 9;141(40):15884-15890. doi: 10.1021/jacs.9b06977. Epub 2019 Sep 30.
coupling is critical to control the dynamics of membrane domain registration/anti-registration, which is important in maintaining proper biological functions. Factors such as lipid acyl chain inter-digitation and membrane remodeling have been found to be able to regulate the coupling. However, detailed molecular mechanisms that dominate the coupling are still far from clear. Here, we revealed that lipid acyl chain double bond position can regulate the coupling according to our coarse-grained and all-atom molecular dynamics simulations. The farther the double bond is away from the lipid tail terminal, the weaker the attractive interactions between unsaturated lipids. Therefore, the relative motions of membrane domains in two membrane leaflets become more obvious (membrane domain anti-registration). Generally, our simulations validated a direct indicator for the coupling strength, which provides physical insights into the molecular mechanisms of membrane domain registration/anti-registration.
脂质酰链双键位置可通过粗粒化和全原子分子动力学模拟调控脂筏耦合
脂筏耦合对于控制脂筏域的注册/反注册动力学至关重要,这对于维持适当的生物功能非常重要。已经发现,诸如脂质酰链交错和膜重塑等因素能够调控脂筏耦合。然而,主导脂筏耦合的详细分子机制仍然远未清楚。在这里,我们根据粗粒化和全原子分子动力学模拟揭示了脂质酰链双键位置可以调控脂筏耦合。双键距脂质尾部末端越远,不饱和脂质之间的吸引力相互作用越弱。因此,两个膜小叶中膜域的相对运动变得更加明显(膜域反注册)。通常,我们的模拟验证了脂筏耦合强度的直接指标,为膜域注册/反注册的分子机制提供了物理见解。