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用于防止蛋白质和肽非特异性吸附的混合聚乙二醇键合链表面的构建。

Creation of a mixed poly(ethylene glycol) tethered-chain surface for preventing the nonspecific adsorption of proteins and peptides.

机构信息

Department of Materials Science, Tokyo University of Science, Noda-shi, Chiba 270-8510, Japan.

出版信息

Biointerphases. 2007 Dec;2(4):126-30. doi: 10.1116/1.2800754.

Abstract

Using a heterotelechelic poly(ethylene glycol) (PEG) possessing a mercapto group at one end and an acetal group at the other end (acetal-PEG-SH), the authors constructed a reactive PEG tethered-chain surface on a surface plasmon sensor (SPR) gold chip for biosensing with high sensitivity. Nonspecific bovine serum albumin adsorption on the PEG tethered-chain surface was significantly influenced by the density of the PEG chain, and was almost completely suppressed by increasing the PEG density through the repetitive treatment of the chip surface with acetal-PEG-SH. The PEG density was increased even more by adding an underbrushed layer made of shorter-PEG-SH-chain molecules (2 kDa, hereafter 2k) to the surface made of longer-PEG-SH-chain molecules (5 kDa, hereafter 5k). SPR measurement then gave an estimate of the adsorption of a series of proteins with varying sizes and isoelectric points on the PEG chain surface having an underbrushed layer (PEG5k/2k surface). As compared to other SPR surfaces, viz., a commercial carboxymethyl dextran and conventional PEG5k tethered-chain surface without an underbrushed layer, the mixed PEG5k/2k surface showed almost complete inhibition of the nonspecific adsorption not only of high-molecular-weight proteins but also of low-molecular-weight peptides.

摘要

利用一端带有巯基、另一端带有缩醛基的杂臂型聚乙二醇(PEG)(缩醛-PEG-SH),作者在表面等离子体传感器(SPR)金芯片上构建了一种具有高灵敏度的反应性 PEG 接枝链表面用于生物传感。PEG 接枝链表面上的非特异性牛血清白蛋白吸附受 PEG 链密度的显著影响,通过用缩醛-PEG-SH 重复处理芯片表面,几乎完全抑制了 PEG 密度的增加。通过在由更长 PEG-SH 链分子(5 kDa,以下简称 5k)组成的表面上添加由更短 PEG-SH 链分子(2 kDa,以下简称 2k)制成的下刷层,PEG 密度得到了进一步增加。然后,SPR 测量估计了具有不同大小和等电点的一系列蛋白质在具有下刷层的 PEG 链表面(PEG5k/2k 表面)上的吸附情况。与其他 SPR 表面(即商业羧甲基葡聚糖和没有下刷层的常规 PEG5k 接枝链表面)相比,混合 PEG5k/2k 表面不仅对高分子量蛋白质,而且对低分子量肽的非特异性吸附几乎完全抑制。

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