In silico investigation of molecular interactions of Volatile Anesthetics: Effects on phospholipid membranes and subcellular targets

E. A. Zizzi, M. Cavaglià, M. Deriu, J. Tuszynski
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Abstract

The ability of anesthetics to reversibly suppress consciousness must reside in the effects exerted onto specific molecular targets. Interactions between Volatile Anesthetics and the phospholipid membrane as well as intracellular tubulin, were investigated using Computational Molecular Modelling, which showed rapid ligand partitioning inside the membrane and significant effects on the mechanical characteristics thereof, while transient binding locations have been found on the tubulin dimer.
挥发性麻醉药分子相互作用的计算机研究:对磷脂膜和亚细胞靶点的影响
麻醉药可逆地抑制意识的能力必须存在于对特定分子目标施加的作用中。利用计算分子模型研究了挥发性麻醉剂与磷脂膜以及细胞内微管蛋白之间的相互作用,结果表明,膜内配体快速分配并对其力学特性产生显著影响,而微管蛋白二聚体上发现了瞬时结合位置。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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