Fábián Balázs, Sega Marcello, Voloshin Vladimir P, Medvedev Nikolai N, Jedlovszky Pál
Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics , Szent Gellért tér 4, H-1111 Budapest, Hungary.
Institut UTINAM (CNRS UMR 6213), Université Bourgogne Franche-Comté , 16 route de Gray, F-25030 Besançon, France.
J Phys Chem B. 2017 Apr 6;121(13):2814-2824. doi: 10.1021/acs.jpcb.7b00990. Epub 2017 Mar 27.
The effect of four general anesthetics, namely chloroform, halothane, diethyl ether, and enflurane on the free volume fraction and lateral pressure profiles in a fully hydrated dipalmitoylphosphatidylcholime (DPPC) membrane is investigated by means of computer simulation. In order to find changes that can be related to the molecular mechanism of anesthesia as well as its pressure reversal, the simulations are performed both at atmospheric and high (1000 bar) pressures. The obtained results show that the additional free volume occurring in the membrane is localized around the anesthetic molecules themselves. Correspondingly, the fraction of the free volume is increased in the outer of the two membrane regions (i.e., at the outer edge of the hydrocarbon phase) where anesthetic molecules prefer to stay in every case. As a consequence, the presence of anesthetics decreases the lateral pressure in the nearby region of the lipid chain ester groups, in which the anesthetic molecules themselves do not penetrate. Both of these changes, occurring upon introducing anesthetics in the membrane, are clearly reverted by the increase of the global pressure. These findings are in accordance both with the more than 60 years old "critical volume hypothesis" of Mullins, and with the more recent "lateral pressure hypothesis" of Cantor. Our results suggest that if anesthesia is indeed caused by conformational changes of certain membrane-bound proteins, induced by changes in the lateral pressure profile, as proposed by Cantor, the relevant conformational changes are expected to occur in the membrane region where the ester groups are located.
通过计算机模拟研究了四种全身麻醉剂,即氯仿、氟烷、乙醚和恩氟烷对完全水合的二棕榈酰磷脂酰胆碱(DPPC)膜中自由体积分数和侧向压力分布的影响。为了找到与麻醉分子机制及其压力反转相关的变化,在大气压和高压(1000巴)下都进行了模拟。所得结果表明,膜中出现的额外自由体积位于麻醉剂分子自身周围。相应地,在两个膜区域中靠近外侧的区域(即烃相的外边缘),自由体积分数增加,在每种情况下麻醉剂分子都倾向于停留在该区域。因此,麻醉剂的存在会降低脂质链酯基团附近区域的侧向压力,而麻醉剂分子本身不会渗透到该区域。在膜中引入麻醉剂时发生的这两种变化,都会随着整体压力的增加而明显逆转。这些发现既符合穆林斯提出的已有60多年历史的“临界体积假说”,也符合坎托最近提出的“侧向压力假说”。我们的结果表明,如果麻醉确实是由坎托提出的侧向压力分布变化诱导的某些膜结合蛋白的构象变化引起的,那么相关的构象变化预计会发生在酯基团所在的膜区域。