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在S层蛋白稳定的脂质双分子层膜中进行长时间随机单离子通道记录。

Prolonged stochastic single ion channel recordings in S-layer protein stabilized lipid bilayer membranes.

作者信息

Keizer Henk M, Andersson Martin, Chase Chris, Laratta William P, Proemsey Josh B, Tabb Joel, Long Joanna R, Duran Randolph S

机构信息

Department of Chemistry, Physical Chemistry, University of Florida, 318 Leigh Hall, FL 32611, Gainesville, USA.

出版信息

Colloids Surf B Biointerfaces. 2008 Sep 1;65(2):178-85. doi: 10.1016/j.colsurfb.2008.04.015. Epub 2008 May 4.

Abstract

S-layer proteins are commonly found in bacteria and archaea as two-dimensional monomolecular crystalline arrays as the outermost cell membrane component. These proteins have the unique property that following disruption by chemical agents, monomers of the protein can re-assemble to their original lattice structure. This unique property makes S-layers interesting for utilization in bio-nanotechnological applications. Here, we show that the addition of S-layer proteins to bilayer lipid membranes increases the lifetime and the stability of the bilayer. M2delta ion channels were functionally incorporated into these S-layer stabilized membranes and we were able to record their activity for up to 20 h. Transmission electron microscopy (TEM) was used to visualize the 2D crystalline pattern of the S-layer and the M2delta ion channel characteristics in bilayer lipid membrane's were compared in the presence and absence of S-layers.

摘要

S层蛋白常见于细菌和古细菌中,作为最外层细胞膜成分以二维单分子晶体阵列形式存在。这些蛋白质具有独特的特性,即在受到化学试剂破坏后,蛋白质单体能够重新组装成其原始晶格结构。这种独特的特性使得S层在生物纳米技术应用中具有利用价值。在此,我们表明向双层脂质膜中添加S层蛋白可增加双层膜的寿命和稳定性。M2δ离子通道功能性地整合到这些S层稳定的膜中,并且我们能够记录它们长达20小时的活性。使用透射电子显微镜(TEM)观察S层的二维晶体图案,并比较了在有和没有S层的情况下双层脂质膜中M2δ离子通道的特性。

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