Frank Reidy Research Center for Bioelectrics, Old Dominion University, Norfolk, VA, 23508, USA.
Department of Physics, Department of Chemistry and Biochemistry, University of California Santa Barbara, Santa Barbara, CA, 93106, USA.
Sci Rep. 2017 Mar 3;7(1):57. doi: 10.1038/s41598-017-00092-0.
The detailed molecular mechanisms underlying the permeabilization of cell membranes by pulsed electric fields (electroporation) remain obscure despite decades of investigative effort. To advance beyond descriptive schematics to the development of robust, predictive models, empirical parameters in existing models must be replaced with physics- and biology-based terms anchored in experimental observations. We report here absolute values for the uptake of YO-PRO-1, a small-molecule fluorescent indicator of membrane integrity, into cells after a single electric pulse lasting only 6 ns. We correlate these measured values, based on fluorescence microphotometry of hundreds of individual cells, with a diffusion-based geometric analysis of pore-mediated transport and with molecular simulations of transport across electropores in a phospholipid bilayer. The results challenge the "drift and diffusion through a pore" model that dominates conventional explanatory schemes for the electroporative transfer of small molecules into cells and point to the necessity for a more complex model.
尽管经过了几十年的研究努力,脉冲电场(电穿孔)使细胞膜穿孔的详细分子机制仍然不清楚。为了超越描述性示意图,开发出强大、可预测的模型,现有模型中的经验参数必须用基于物理和生物学的术语来代替,这些术语基于实验观察。我们在这里报告了在持续仅 6ns 的单个电脉冲之后,小分子荧光膜完整性指示剂 YO-PRO-1 进入细胞的吸收的绝对值。我们将这些基于数百个单个细胞荧光显微光度测定的测量值与基于孔介导运输的扩散的几何分析以及跨磷脂双层中电孔的运输的分子模拟相关联。结果挑战了主导小分子经电穿孔进入细胞的传统解释方案的“通过孔的漂移和扩散”模型,并指出需要更复杂的模型。