White Ryan J, Ervin Eric N, Yang Tinglu, Chen Xin, Daniel Susan, Cremer Paul S, White Henry S
Department of Chemistry, University of Utah, 315 S 1400 E, Salt Lake City, Utah 84112, USA.
J Am Chem Soc. 2007 Sep 26;129(38):11766-75. doi: 10.1021/ja073174q. Epub 2007 Sep 5.
Protein ion-channel recordings using a glass nanopore (GNP) membrane as the support structure for lipid bilayer membranes are presented. The GNP membrane is composed of a single conical-shaped nanopore embedded in a approximately 50 microm-thick glass membrane chemically modified with a 3-cyanopropyldimethylchlorosilane monolayer to produce a surface of intermediate hydrophobicity. This surface modification results in lipid monolayer formation on the glass surface and a lipid bilayer suspended across the small orifice (100-400 nm-radius) of the GNP membrane, while allowing aqueous solutions to fully wet the glass nanopore. The GNP membrane/bilayer structures, which exhibit ohmic seal resistances of approximately 70 GOmega and electrical breakdown voltages of approximately 0.8 V, are exceptionally stable to mechanical disturbances and have lifetimes of at least 2 weeks. These favorable characteristics result from the very small area of bilayer (10(-10)-10(-8) cm(2)) that is suspended across the GNP membrane orifice. Fluorescence microscopy and vibrational sum frequency spectroscopy demonstrate that a lipid monolayer forms on the 3-cyanopropyl-dimethylchlorosilane modified glass surface with the lipid tails oriented toward the glass. The GNP membrane/bilayer structure is well suited for single ion-channel recordings. Reproducible insertion of the protein ion channel, wild-type alpha-hemolysin (WTalphaHL), and stochastic detection of a small molecule, heptakis(6-O-sulfo)-beta-cyclodextrin, are demonstrated. In addition, the insertion and removal of WTalphaHL channels are reproducibly controlled by applying small pressures (-100 to 350 mmHg) across the lipid bilayer. The electrical and mechanical stability of the bilayer, the ease of which bilayer formation is achieved, and the ability to control ion-channel insertion, coupled with the small bilayer capacitance of the GNP membrane-based system, provide a new and nearly optimal system for single ion-channel recordings.
本文介绍了使用玻璃纳米孔(GNP)膜作为脂质双层膜支撑结构的蛋白质离子通道记录。GNP膜由嵌入约50微米厚玻璃膜中的单个锥形纳米孔组成,该玻璃膜用3-氰丙基二甲基氯硅烷单层进行化学修饰,以产生中等疏水性表面。这种表面修饰导致在玻璃表面形成脂质单层,并在GNP膜的小孔(半径100 - 400纳米)上悬浮脂质双层,同时允许水溶液完全润湿玻璃纳米孔。GNP膜/双层结构表现出约70 GΩ的欧姆封接电阻和约0.8 V的电击穿电压,对机械干扰异常稳定,寿命至少为2周。这些良好特性源于跨GNP膜孔悬浮的双层膜面积非常小(10^(-10) - 10^(-8)平方厘米)。荧光显微镜和振动和频光谱表明,在3-氰丙基二甲基氯硅烷修饰的玻璃表面形成了脂质单层,脂质尾部朝向玻璃。GNP膜/双层结构非常适合单离子通道记录。展示了蛋白质离子通道野生型α-溶血素(WTαHL)的可重复插入以及小分子七(6-O-磺基)-β-环糊精的随机检测。此外,通过在脂质双层上施加小压力(-100至350 mmHg),可重复控制WTαHL通道的插入和移除。双层膜的电气和机械稳定性、形成双层膜的容易程度、控制离子通道插入的能力,以及基于GNP膜系统的小双层电容,为单离子通道记录提供了一个新的且近乎最佳的系统。