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基于分子动力学的痕量胺膜通透性模拟。

Molecular dynamics-based simulation of trace amine membrane permeability.

机构信息

Department of Chemistry, Brandon University, 270 18th Street, Brandon, MB, R7A 6A9, Canada.

出版信息

J Neural Transm (Vienna). 2011 Jul;118(7):1119-28. doi: 10.1007/s00702-010-0569-2. Epub 2011 Jan 6.

Abstract

Trace amines are endogenous compounds, typified by 2-phenylethylamine (PE) and p-tyramine (TA), found in the vertebrate central nervous system. Although synthesized in pre-synaptic terminals, trace amines do not appear to act as neurotransmitters, but rather modulate responsivity to co-existing neurotransmitters. Trace amines are neither actively accumulated in synaptic vesicles, nor released in an activity-dependent manner. Further, Trace Amine-Associated Receptor 1 (TAAR1), which is selectively activated by PE and TA, is intracellular. As such, PE and TA need to cross cell membranes in order to exert their effects. This has been assumed to occur by simple diffusion, but has not previously been systematically examined. Experimental data were obtained using Fluorosome(®) technology. A permeability coefficient of 25.3 ± 3.8 Å/s (n = 6) was obtained for TA which was not significantly different from that obtained for the monoamine neurotransmitter noradrenaline (20.3 ± 3.8 Å/s, n = 8). PE was unsuitable for use with this system. We have also used molecular dynamics computer simulation techniques to determine the potential of mean force (PMF) associated with trace amine passage across lipid bilayers. A PMF peak barrier of 25 ± 6 kcal/mol (protonated) and 13 ± 1 kcal/mol (deprotonated) was obtained for PE. Protonated TA peak energy barriers were even greater at 31 ± 1 kcal/mol. Application of a homogeneous solubility-diffusion model combining the measured permeability coefficients and simulated PMF allows fitting of the diffusion coefficient for trace amines in the hydrophobic region of the lipid bilayer. The diffusion coefficients in other regions of the membrane were found to make negligible contributions to the permeability coefficient for the calculated PMF. The fit obtained a value for the diffusion coefficient of (163 ± 25) × 10(-10) m(2)/s for TA(+) in the hydrophobic core region. The diffusion coefficient for TA(+) in the aqueous compartment was also calculated directly by simulation yielding a value of (0.62 ± 0.26) × 10(-10) m(2)/s. The adopted simulation methods failed to yield diffusion coefficients in the core region indicating that further work will be required to accurately predict permeability coefficients for trace amines passing through membranes.

摘要

痕量胺是内源性化合物,以 2-苯乙胺 (PE) 和对羟苯乙胺 (TA) 为代表,存在于脊椎动物中枢神经系统中。尽管痕量胺在突触前末端合成,但它们似乎不作为神经递质发挥作用,而是调节对共存神经递质的反应性。痕量胺既不主动积累在突触小泡中,也不以活动依赖的方式释放。此外,痕量胺相关受体 1 (TAAR1) 被 PE 和 TA 选择性激活,它位于细胞内。因此,PE 和 TA 需要穿过细胞膜才能发挥作用。人们一直认为这是通过简单的扩散来实现的,但以前并没有系统地检查过。实验数据是使用 Fluorosome(®) 技术获得的。TA 的渗透系数为 25.3 ± 3.8 Å/s(n = 6),与单胺神经递质去甲肾上腺素的渗透系数(20.3 ± 3.8 Å/s,n = 8)没有显著差异。PE 不适合用于此系统。我们还使用分子动力学计算机模拟技术来确定痕量胺穿过脂质双层的平均力势 (PMF) 相关的潜力。PE 质子化和去质子化的 PMF 峰势垒分别为 25 ± 6 kcal/mol 和 13 ± 1 kcal/mol。质子化 TA 的峰能量势垒甚至更大,为 31 ± 1 kcal/mol。应用一种结合测量渗透率系数和模拟 PMF 的均匀溶解度-扩散模型,可以拟合痕量胺在脂质双层疏水区的扩散系数。发现膜的其他区域的扩散系数对计算的 PMF 渗透率系数的贡献可以忽略不计。拟合得到 TA(+)在疏水区的扩散系数为(163 ± 25)×10(-10)m(2)/s。通过模拟直接计算 TA(+)在水相区的扩散系数,得到的值为(0.62 ± 0.26)×10(-10)m(2)/s。采用的模拟方法未能在核心区域得到扩散系数,表明需要进一步的工作来准确预测通过膜的痕量胺的渗透率系数。

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