Ziegler Matthew J, Vernier P Thomas
Mork Family Department of Chemical Engineering and Materials Science, Viterbi School of Engineering, University of Southern California, Los Angeles, California 90089-0271, USA.
J Phys Chem B. 2008 Oct 30;112(43):13588-96. doi: 10.1021/jp8027726. Epub 2008 Oct 7.
Lipid bilayers, normally a barrier to charged species and large molecules, are permeabilized by electric fields, a phenomenon exploited by cell biologists and geneticists for porating and transfecting cells and tissues. Recent molecular simulation studies have advanced our understanding of electroporation, but the relative contributions of atomically local details (interface water and headgroup dipole and counterion configurations) and medium- and long-range electrostatic gradients and changes in membrane structural shifts to the initiating conditions and mechanisms of pore formation remain unclear. Molecular dynamics simulations of electroporation in several lipid systems presented here reveal the effects of lipid hydrocarbon tail length and composition on the magnitude of the field required for poration and on the location of the initial sites of field-driven water intrusion into the bilayer. Minimum porating external fields of 260 mV nm(-1), 280 mV nm(-1), 320 mV nm(-1), and 380 mV nm(-1) were found for 1,2-dilauroyl-sn-glycero-3-phosphatidylcholine (DLPC), 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine (POPC), and 1,2-dioleoyl- sn-glycero-3-phosphatidylcholine (DOPC) bilayers, respectively, and correlated most strongly with the bilayer thickness. These phospholipid systems share several common features including a wide, dynamic distribution of the headgroup dipole angle with the bilayer normal ranging from 0 to 155 degrees that is only slightly shifted in a porating electric field, and similar electric field-induced shifts in water dipole orientation, although the mean water dipole moment profile at the aqueous-membrane interface is more sensitive to the electric field for DOPC than for the other phospholipids. The location of pore initiation, at the anode- or cathode-facing leaflet, varies with the composition of the bilayer and correlates with a change in the polarity of the localized electric field at the interface.
脂质双层通常是带电物质和大分子的屏障,但电场可使其通透,细胞生物学家和遗传学家利用这一现象对细胞和组织进行穿孔和转染。最近的分子模拟研究增进了我们对电穿孔的理解,但原子局部细节(界面水、头基偶极和抗衡离子构型)以及中长程静电梯度和膜结构变化对孔形成的起始条件和机制的相对贡献仍不清楚。本文介绍的几种脂质系统中电穿孔的分子动力学模拟揭示了脂质烃链长度和组成对穿孔所需电场强度以及电场驱动水侵入双层的起始位置的影响。对于1,2-二月桂酰-sn-甘油-3-磷酸胆碱(DLPC)、1,2-二棕榈酰-sn-甘油-3-磷酸胆碱(DPPC)、1-棕榈酰-2-油酰-sn-甘油-3-磷酸胆碱(POPC)和1,2-二油酰-sn-甘油-3-磷酸胆碱(DOPC)双层膜,分别发现最小穿孔外场为260 mV nm⁻¹、280 mV nm⁻¹、320 mV nm⁻¹和380 mV nm⁻¹,且与双层膜厚度的相关性最强。这些磷脂系统具有几个共同特征,包括头基偶极角与双层膜法线的广泛动态分布,范围从0到155度,在穿孔电场中仅略有偏移,以及类似的电场诱导水偶极取向变化,尽管水-膜界面处的平均水偶极矩分布对DOPC的电场比其他磷脂更敏感。孔起始的位置,在面向阳极或阴极的小叶上,随双层膜的组成而变化,并与界面处局部电场的极性变化相关。