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Reactive oxygen species at phospholipid bilayers: Distribution, mobility and permeation

机译:磷脂双层的反应性氧物种:分布,迁移率和渗透

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Reactive oxygen species (ROS) are involved in biochemical processes such as redox signaling, aging, carcinogenesis and neurodegeneration. Although biomembranes are targets for reactive oxygen species attack, little is known about the role of their specific interactions. Here, molecular dynamics simulations were employed to determine the distribution, mobility and residence times of various reactive oxygen species at the membrane-water interface. Simulations showed that molecular oxygen (O-2) accumulated at the membrane interior. The applicability of this result to singlet oxygen (O-2(-)) was discussed. Conversely, superoxide (Cc) radicals and hydrogen peroxide (H2O2) remained at the aqueous phase. Both hydroxyl (HO) and hydroperoxyl (HO2) radicals were able to penetrate deep into the lipid headgroups region. Due to membrane fluidity and disorder, these radicals had access to potential peroxidation sites along the lipid hydrocarbon chains, without having to overcome the permeation free energy barrier. Strikingly, HO2 radicals were an order of magnitude more concentrated in the headgroups region than in water, implying a large shift in the acid-base equilibrium between HO2 and O. In comparison with O-2, both HO and HO2 radicals had lower lateral mobility at the membrane. Simulations revealed that there were intermittent interruptions in the H-bond network around the HO radicals at the headgroups region. This effect is expected to be unfavorable for the H-transfer mechanism involved in HO diffusion. The implications for lipid peroxidation and for the effectiveness of membrane antioxidants were evaluated. (C) 2013 Elsevier B.V. All rights reserved.
机译:活性氧物质(ROS)参与生化过程,如氧化还原信号,老化,致癌和神经变性。虽然生物膜是反应性氧物种攻击的靶标,但关于其特异性相互作用的作用毫无少。这里,采用分子动力学模拟来确定膜 - 水界面在各种反应性氧物质的分布,迁移率和停留时间。模拟表明,在膜内部积聚的分子氧(O-2)。讨论了这一结果的适用性(O-2())。相反,超氧化物(CC)自由基和过氧化氢(H 2 O 2)残留在水相。羟(HO)和氢过氧基(HO2)的基团都能够深入渗透到脂质头组区域中。由于膜流动性和紊乱,这些自由基可以沿着脂质烃链进入潜在的过氧化位点,而不必克服渗透自由能屏障。尖锐地,HO2基团比在头组区域中更浓缩的数量级,暗示HO2和O之间的酸碱平衡均匀偏移。与O-2相比,HO和HO2基团都具有较低的横向迁移率在膜上。仿真显示,在头组区域周围的H键网络中的H键网络中中断。预计该效果将不利于何种扩散中涉及的H转移机制。评估对脂质过氧化和膜抗氧化剂的有效性的影响。 (c)2013年elestvier b.v.保留所有权利。

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