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用玻璃微电极刺穿的巨型脂质囊泡:通过膜铺展形成千兆欧密封。

Giant lipid vesicles impaled with glass microelectrodes: GigaOhm seal by membrane spreading.

作者信息

Reccius Christian H, Fromherz Peter

机构信息

Department of Membrane and Neurophysics, Max Planck Institute for Biochemistry, Martinsried/München, Germany 82152.

出版信息

Langmuir. 2004 Dec 7;20(25):11175-82. doi: 10.1021/la048233h.

DOI:10.1021/la048233h
PMID:15568873
Abstract

Giant unilamellar lipid vesicles could be perfect systems to study ion channels in the environment of lipid membranes with defined chemical and physical properties. Prerequisite for electrical measurements is an intravesicular electrical contact. We describe the impalement of giant lipid vesicles by glass micropipet electrodes with a tight seal. To avoid displacement or burst during impalement, the vesicles are immobilized in relaxed conditions by microscopic picket fences of polyimide. The outer surface of the pipets is selectively coated with silanes or polylysine. Structurally, the impalement is verified by ejecting a fluorescent solution out of the pipet. For electrical characterization, current pulses are applied to the pipet and voltage transients are recorded. The data are evaluated in terms of the capacitance and effective resistance of the membrane. Directly after impalement, we observe a seal resistance up to 1.2 GOmega that continuously decays within a period of up to 20 min until it suddenly disappears without burst of the vesicle. During impalement, a spreading of the vesicle membrane along the outer surface of the pipets is observed using a fluorescent membrane-bound dye. We assign the tight pipet-vesicle contact to spreading of the lipid bilayer by a rolling mechanism and the loss of resistance to micro- and macropores that are induced by the resulting membrane tension. Limitation of spreading is attempted with barriers on the pipet.

摘要

巨型单层脂质囊泡可能是在具有明确化学和物理性质的脂质膜环境中研究离子通道的理想体系。进行电学测量的前提是囊泡内要有电接触。我们描述了用玻璃微吸管电极紧密密封刺入巨型脂质囊泡的方法。为避免刺入过程中囊泡移位或破裂,通过聚酰亚胺的微观栅栏将囊泡固定在松弛状态。吸管的外表面选择性地涂有硅烷或聚赖氨酸。从结构上看,通过从吸管中喷出荧光溶液来验证刺入情况。为进行电学表征,向吸管施加电流脉冲并记录电压瞬变。根据膜的电容和有效电阻对数据进行评估。刺入后立即观察到密封电阻高达1.2千兆欧,在长达20分钟的时间内持续衰减,直到突然消失而囊泡未破裂。在刺入过程中,使用荧光膜结合染料观察到囊泡膜沿吸管外表面展开。我们将紧密的吸管 - 囊泡接触归因于脂质双层通过滚动机制展开,以及电阻的丧失归因于由此产生的膜张力诱导的微孔和大孔。尝试通过在吸管上设置屏障来限制展开。

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