Leng Xiaoling, Kinnun Jacob J, Marquardt Drew, Ghefli Mikel, Kučerka Norbert, Katsaras John, Atkinson Jeffrey, Harroun Thad A, Feller Scott E, Wassall Stephen R
Department of Physics, Indiana University-Purdue University Indianapolis, Indianapolis, Indiana.
Department of Physics, Brock University, St. Catharines, Ontario, Canada; Institute of Molecular Biosciences, University of Graz, Graz, Austria.
Biophys J. 2015 Oct 20;109(8):1608-18. doi: 10.1016/j.bpj.2015.08.032.
The presumptive function for alpha-tocopherol (αtoc) in membranes is to protect polyunsaturated lipids against oxidation. Although the chemistry of the process is well established, the role played by molecular structure that we address here with atomistic molecular-dynamics simulations remains controversial. The simulations were run in the constant particle NPT ensemble on hydrated lipid bilayers composed of SDPC (1-stearoyl-2-docosahexaenoylphosphatidylcholine, 18:0-22:6PC) and SOPC (1-stearoyl-2-oleoylphosphatidylcholine, 18:0-18:1PC) in the presence of 20 mol % αtoc at 37°C. SDPC with SA (stearic acid) for the sn-1 chain and DHA (docosahexaenoic acid) for the sn-2 chain is representative of polyunsaturated phospholipids, while SOPC with OA (oleic acid) substituted for the sn-2 chain serves as a monounsaturated control. Solid-state (2)H nuclear magnetic resonance and neutron diffraction experiments provide validation. The simulations demonstrate that high disorder enhances the probability that DHA chains at the sn-2 position in SDPC rise up to the bilayer surface, whereby they encounter the chromanol group on αtoc molecules. This behavior is reflected in the van der Waals energy of interaction between αtoc and acyl chains, and illustrated by density maps of distribution for acyl chains around αtoc molecules that were constructed. An ability to more easily penetrate deep into the bilayer is another attribute conferred upon the chromanol group in αtoc by the high disorder possessed by DHA. By examining the trajectory of single molecules, we found that αtoc flip-flops across the SDPC bilayer on a submicrosecond timescale that is an order-of-magnitude greater than in SOPC. Our results reveal mechanisms by which the sacrificial hydroxyl group on the chromanol group can trap lipid peroxyl radicals within the interior and near the surface of a polyunsaturated membrane. At the same time, water-soluble reducing agents that regenerate αtoc can access the chromanol group when it locates at the surface.
α-生育酚(αtoc)在细胞膜中的假定功能是保护多不饱和脂质免受氧化。尽管该过程的化学原理已得到充分确立,但我们在此通过原子分子动力学模拟研究的分子结构所起的作用仍存在争议。模拟在恒定粒子数的NPT系综中进行,体系为含有20 mol% αtoc的水合脂质双层,该脂质双层由SDPC(1-硬脂酰-2-二十二碳六烯酰磷脂酰胆碱,18:0-22:6PC)和SOPC(1-硬脂酰-2-油酰磷脂酰胆碱,18:0-18:1PC)组成,温度为37°C。sn-1链为SA(硬脂酸)且sn-2链为DHA(二十二碳六烯酸)的SDPC代表多不饱和磷脂,而sn-2链被OA(油酸)取代的SOPC用作单不饱和对照。固态(2)H核磁共振和中子衍射实验提供了验证。模拟表明,高无序性增加了SDPC中sn-2位的DHA链上升到双层表面的概率,从而使其与αtoc分子上的色满醇基团相遇。这种行为反映在αtoc与酰基链之间的范德华相互作用能中,并通过构建的αtoc分子周围酰基链分布的密度图得以说明。DHA具有的高无序性赋予αtoc分子中的色满醇基团的另一个特性是更容易深入双层内部。通过检查单个分子的轨迹,我们发现αtoc在亚微秒时间尺度内跨越SDPC双层翻转,这比在SOPC中快一个数量级。我们的结果揭示了色满醇基团上的牺牲性羟基能够在多不饱和膜内部和表面附近捕获脂质过氧自由基的机制。同时,当色满醇基团位于表面时,能使αtoc再生的水溶性还原剂可以接近该基团。