传感器类型
其他(可储存液滴界面脂质双分子层离子通道平台)
检测对象
α-溶血素(alpha-hemolysin, aHL)、短杆菌肽A(gramicidin A, gA)的单通道电导;样品基质:人工液滴界面脂质双分子层(DIB)水相/有机相体系。
检测原理
系统将含脂质和通道蛋白的液滴界面膜前体在-80°C甲醇中快速冷冻储存。解冻后,水相液滴先融化并在重力作用下落入水/有机界面,与预先稳定的脂质单体层自组装形成液滴界面双分子层(DIB)。Ag/AgCl电极施加偏压,膜形成过程表现为电容电流增加,成熟膜具有吉欧级电阻和约480 nF/cm2比电容。aHL七聚体纳米孔或gA二聚体通道插入膜后,在50 mV或40 mV偏压下允许离子跨膜流动,产生约0.8 nS的离散电流台阶或二聚体结合/解离事件。放大器记录电流,数字显微镜同步监测膜面积,从而将通道开放数量与电导变化转换为可定量电信号。
检测灵敏度
原文未报告 LOD、线性范围、灵敏度斜率或相关系数。
效应效果
该平台形成的DIB寿命超过7 h,膜厚约4 nm,比电容约480 nF/cm2,密封电阻达吉欧级,噪声水平与传统脂质双分子层体系相当。aHL插入后在1 h内形成纳米孔,单通道电导约0.8 nS,电流台阶离散;gA显示典型二聚体结合/解离事件,证明平台支持低噪声单通道记录。系统无需复杂膜制备操作,冷冻状态下可长期储存和运输,解冻后自动成膜,并可扩展至96或384孔板用于高通量筛选。作者认为其可提高离子通道研究可及性,适用于药物筛选、生物传感器组件和生物物理研究。
传感器的构成
- 基底/换能器电极:4 mL 玻璃瓶底部 Ag/AgCl 电极,提供跨膜电流测量回路
- 插入液滴电极:208 μm 银丝 Ag/AgCl 电极,插入水相液滴测量跨膜电流
- 水相缓冲层:1 M KCl、1 mM EDTA、10 mM Tris-HCl(pH 8.0),提供离子导电环境并稳定膜界面
- 有机相/脂质单体层:十六烷与正癸烷 4:1 混合溶剂含 3% (w/w) asolectin,形成可冷冻脂质单体层
- 液滴界面双分子层:0.5 μL 水相液滴解冻后落入界面,与脂质单体层自组装形成 DIB
- 功能通道元件:alpha-hemolysin (aHL) 或 gramicidin A (gA),插入双分子层形成纳米孔/离子通道
- 信号读出:Axopatch 200B 放大器、DigiData 1332 DAQ 与数字显微镜,记录电容/单通道电流并光学监测膜
中文摘要
人工脂质双分子层是研究离子通道及构建工程化生物传感器的重要平台,但传统方法制备的双分子层脆弱、寿命短,且单通道测量依赖专业操作,限制了实际应用。本文报道一种可储存的液滴界面脂质双分子层前体:将含脂质和离子通道的水相液滴与有机相一起快速冷冻,解冻后水相液滴在重力作用下落入水/有机界面,自发形成液滴界面双分子层(DIB)。该方法制备的膜具有吉欧级电阻和典型比电容,噪声水平与传统体系相当。随后将α-溶血素和短杆菌肽A插入膜中,观察到与文献一致的单通道电导。该平台从制备到使用可自动化,冷冻状态下可长期储存,使离子通道测量可在不同地点进行,有望用于生物传感器、离子通道药物筛选和生物物理研究。
英文摘要
An artificially created lipid bilayer is an important platform in studying ion channels and engineered biosensor applications. However, a lipid bilayer created using conventional techniques is fragile and short-lived, and the measurement of ion channels requires expertise and laborious procedures, precluding practical applications. Here, we demonstrate a storable droplet lipid bilayer precursor frozen with ion channels, resulting in a droplet interface bilayer upon thawing. A small vial with an aqueous droplet in organic solution was flash frozen in -80 °C methanol immediately after an aqueous droplet was introduced into the organic solution and gravity draws the droplet down to the interface upon thawing. A lipid bilayer created along the interface using this method had giga-ohm resistance and typical specific capacitance values. The noise level of this system is favorably comparable to the conventional system. The subsequent incorporation of ion channels, alpha-hemolysin and gramicidin A, showed typical conductance values consistent with those in previous literatures. This novel system to create a lipid bilayer as a whole can be automated from its manufacture to use and indefinitely stored when frozen. As a result, ion channel measurements can be carried out in any place, increasing the accessibility of ion channel studies as well as a number of applications, such as biosensors, ion channel drug screening, and biophysical studies.