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在仿生嵌段共聚物中重构的短杆菌肽和短杆菌肽S的平面双层测量

Planar Bilayer Measurements of Alamethicin and Gramicidin Reconstituted in Biomimetic Block Copolymers.

作者信息

Martin Michael, Dubbs Timothy, Fried J R

机构信息

Department of Chemical Engineering, University of Louisville , Louisville, Kentucky 40292, United States.

出版信息

Langmuir. 2017 Feb 7;33(5):1171-1179. doi: 10.1021/acs.langmuir.6b03309. Epub 2017 Jan 24.

Abstract

This work explores methods for forming and characterizing biomimetic planar membranes composed of amphiphilic block copolymers. The membranes are diblocks and triblocks with hydrophilic blocks of poly(2-methyl-2-oxazoline) (PMOXA) and hydrophobic blocks of poly(dimethylsiloxane) (PDMS). Experiments with the lipid diphytanoyl phosphocholine (DPhPC) serve as a basis for comparison with the polymeric membranes. Phase-contrast microscopy is used to study how membranes evolve over time after their formation. Capacitance measurements as a function of the thinned membrane area (prepared from two separate solvent systems) are performed to clarify the importance of the Plateau-Gibbs border in electrical measurements. Finally, functional reconstitution of the two ion channels, alamethicin and gramicidin, is investigated. Imaging in transmitted phase-contrast mode provides visualization of thinned regions that contain monolayers or bilayers (in the case of diblock copolymer). The specific capacitance measurements yield 0.28 μF/cm with a corresponding thickness of 8.5 nm for PMOXA-PDMS-PMOXA (blocks of 6 PMOXA and 35 PDMS repeat units) formed from a solution of ethanol-decane, 0.55 μF/cm and 4.4 nm in chloroform-toluene, and 0.46 μF/cm and 5.4 nm for the diblock PMOXA-PDMS in ethanol-decane. Alamethicin reconstitution in the block copolymers shows slower channel-forming kinetics with somewhat higher conductance values than found in DPhPC. Gramicidin in the block copolymer shows a slightly voltage-dependent conductance as a function of time, with little stochastic conductance state switching, in contrast to reconstitution in DPhPC where gramicidin switches states at ∼3 Hz.

摘要

这项工作探索了形成和表征由两亲性嵌段共聚物组成的仿生平面膜的方法。这些膜是具有聚(2-甲基-2-恶唑啉)(PMOXA)亲水嵌段和聚(二甲基硅氧烷)(PDMS)疏水嵌段的二嵌段和三嵌段共聚物。使用脂质二植烷酰磷脂酰胆碱(DPhPC)进行的实验作为与聚合物膜比较的基础。相差显微镜用于研究膜形成后随时间的演变。进行电容测量作为变薄膜面积(由两种不同的溶剂体系制备)的函数,以阐明普拉托-吉布斯边界在电学测量中的重要性。最后,研究了两种离子通道,即短杆菌肽A和短杆菌肽的功能重构。透射相差模式成像提供了包含单层或双层(对于二嵌段共聚物而言)的变薄区域的可视化。对于由乙醇-癸烷溶液形成的PMOXA-PDMS-PMOXA(6个PMOXA嵌段和35个PDMS重复单元),比电容测量结果为0.28 μF/cm,相应厚度为8.5 nm;在氯仿-甲苯中为0.55 μF/cm和4.4 nm;对于乙醇-癸烷中的二嵌段PMOXA-PDMS为0.46 μF/cm和5.4 nm。在嵌段共聚物中重构短杆菌肽A显示出较慢的通道形成动力学,其电导值略高于在DPhPC中发现的值。与在DPhPC中重构时短杆菌肽以约3 Hz的频率切换状态相反,嵌段共聚物中的短杆菌肽显示出略微依赖电压的电导随时间变化,且几乎没有随机的电导状态切换。

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