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体外细胞电通透后小分子摄取的定量模型。

Quantitative model of small molecules uptake after in vitro cell electropermeabilization.

作者信息

Puc Marko, Kotnik Tadej, Mir Lluis M, Miklavcic Damijan

机构信息

Faculty of Electrical Engineering, University of Ljubljana, Trzaska 25, SI-1000 Ljubljana, Slovenia.

出版信息

Bioelectrochemistry. 2003 Aug;60(1-2):1-10. doi: 10.1016/s1567-5394(03)00021-5.

Abstract

Electropermeabilization of the cell membrane is a phenomenon caused by exposure of the cell to electric pulses. Permeabilization depends on pulse duration, pulse amplitude, the number of pulses delivered, and also on other experimental conditions. With these parameters properly chosen, the process of permeabilization is reversible and cells return to their normal physiological state. This article describes the development of a model of diffusion-driven transmembrane transport of small molecules caused by electropermeabilization. The process of permeabilization is divided into a short permeabilizing phase that takes place during the pulse, and a longer resealing phase that begins after the end of the pulse. Because both phases of permeabilization are important for uptake of molecules into cells, most of the effort is focused on the optimization of parameters that influence the flow between intracellular and extracellular space. The model describes well the transmembrane transport caused by electropermeabilization, allowing to study the uptake of molecules as a function of elapsed time, voltage and pulse duration. In addition, our results show that the shapes of the curves of cell permeabilization and survival as functions of pulse amplitude can to a large extent be explained by cell size distribution.

摘要

细胞膜的电通透化是细胞暴露于电脉冲所引起的一种现象。通透化程度取决于脉冲持续时间、脉冲幅度、施加的脉冲数量,还取决于其他实验条件。若这些参数选择得当,通透化过程是可逆的,细胞会恢复到正常生理状态。本文描述了一种由电通透化引起的小分子扩散驱动跨膜运输模型的建立。通透化过程分为在脉冲期间发生的短暂通透化阶段和在脉冲结束后开始的较长的重新封闭阶段。由于通透化的两个阶段对于分子进入细胞都很重要,因此大部分工作都集中在优化影响细胞内和细胞外空间之间物质流动的参数上。该模型很好地描述了由电通透化引起的跨膜运输,能够研究分子摄取量随时间、电压和脉冲持续时间的变化情况。此外,我们的结果表明,细胞通透化曲线和存活曲线作为脉冲幅度函数的形状在很大程度上可以由细胞大小分布来解释。

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