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玻璃双层黏附性的玻璃管中的脂双层力学性质。

Lipid bilayer mechanics in a pipette with glass-bilayer adhesion.

机构信息

Department of Applied Physics, California Institute of Technology, Pasadena, California, USA.

出版信息

Biophys J. 2011 Oct 19;101(8):1913-20. doi: 10.1016/j.bpj.2011.08.057.

Abstract

Electrophysiology is a central tool for measuring how different driving forces (e.g., ligand concentration, transmembrane voltage, or lateral tension) cause a channel protein to gate. Upon formation of the high resistance seal between a lipid bilayer and a glass pipette, the so-called "giga-seal", channel activity can be recorded electrically. In this article, we explore the implications of giga-seal formation on the mechanical state of a lipid bilayer patch. We use a mechanical model for the free energy of bilayer geometry in the presence of glass-bilayer adhesion to draw three potentially important conclusions. First, we use our adhesion model to derive an explicit relationship between applied pressure and patch shape that is consistent with the Laplace-Young Law, giving an alternative method of calculating patch tension under pressure. With knowledge of the adhesion constant, which we find to be in the range ∼0.4-4 mN/m, and the pipette size, one can precisely calculate the patch tension as a function of pressure, without the difficultly of obtaining an optical measurement of the bilayer radius of curvature. Second, we use data from previous electrophysiological experiments to show that over a wide range of lipids, the resting tension on a electrophysiological patch is highly variable and can be 10-100 times higher than estimates of the tension in a typical cell membrane. This suggests that electrophysiological experiments may be systematically altering channel-gating characteristics and querying the channels under conditions that are not the same as their physiological counterparts. Third, we show that reversible adhesion leads to a predictable change in the population response of gating channels in a bilayer patch.

摘要

电生理学是一种用于测量不同驱动力(例如配体浓度、跨膜电压或横向张力)如何导致通道蛋白门控的核心工具。在脂质双层和玻璃吸管之间形成所谓的“千兆密封”高电阻密封后,可以电记录通道活性。在本文中,我们探讨了千兆密封形成对脂质双层斑块机械状态的影响。我们使用玻璃 - 双层粘附存在时的双层几何形状的自由能力学模型来得出三个可能重要的结论。首先,我们使用我们的粘附模型来推导出一个应用压力和斑块形状之间的明确关系,该关系与拉普拉斯 - 杨定律一致,为在压力下计算斑块张力提供了一种替代方法。了解粘附常数,我们发现其范围在 0.4-4 mN/m 之间,以及吸管的尺寸,可以精确地计算出压力下的斑块张力,而无需费力地获得光学测量双层曲率半径。其次,我们使用以前的电生理实验数据表明,在广泛的脂质范围内,电生理斑块上的静息张力高度可变,并且可以比典型细胞膜张力的估计值高 10-100 倍。这表明电生理实验可能会系统地改变通道门控特性,并在与生理对照不同的条件下询问通道。第三,我们表明,可逆粘附会导致双层斑块中门控通道的群体反应发生可预测的变化。

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