蛋白质在聚乙二醇封端的烷硫醇自组装单分子层上的吸附:抗污染行为的分子基础。

Protein adsorption on oligo(ethylene glycol)-terminated alkanethiolate self-assembled monolayers: The molecular basis for nonfouling behavior.

作者信息

Li Lingyan, Chen Shengfu, Zheng Jie, Ratner Buddy D, Jiang Shaoyi

机构信息

Department of Chemical Engineering, University of Washington, Seattle, Washington 98105, USA.

出版信息

J Phys Chem B. 2005 Feb 24;109(7):2934-41. doi: 10.1021/jp0473321.

Abstract

A study of protein resistance of oligo(ethylene glycol) (OEG), HS(CH2)11(OCH2CH2)nOH (n = 2, 4, and 6), self-assembled monolayers (SAMs) on Au(111) surfaces is presented here. Hydroxyl-terminated OEG-SAMs are chosen to avoid the hydrophobic effect observed with methyl-terminated OEG-SAMs, particularly at high packing densities. The structure of the OEG-SAM surfaces is controlled by adjusting the assembly solvent. These SAMs were characterized by X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM). Protein adsorption on these surfaces was investigated by surface plasmon resonance (SPR). OEG-SAMs assembled from mixed ethanol and water solutions show higher packing density on gold than those from pure ethanol solution. For EG2OH- and EG4OH-SAMs, proteins (i.e., fibrinogen and lysozyme) adsorb more on the densely packed SAMs prepared from mixed ethanol and water solutions, while EG6OH-SAMs generally resist protein adsorption regardless of the assembly solvent used.

摘要

本文介绍了在金(111)表面上对低聚乙二醇(OEG)、HS(CH2)11(OCH2CH2)nOH(n = 2、4和6)自组装单分子层(SAMs)的蛋白质抗性研究。选择羟基封端的OEG-SAMs以避免观察到的甲基封端的OEG-SAMs的疏水效应,特别是在高堆积密度下。通过调节组装溶剂来控制OEG-SAM表面的结构。这些SAMs通过X射线光电子能谱(XPS)和原子力显微镜(AFM)进行表征。通过表面等离子体共振(SPR)研究了蛋白质在这些表面上的吸附。由乙醇和水溶液混合组装的OEG-SAMs在金表面上显示出比纯乙醇溶液组装的更高的堆积密度。对于EG2OH-和EG4OH-SAMs,蛋白质(即纤维蛋白原和溶菌酶)在由乙醇和水溶液混合制备的密集堆积的SAMs上吸附更多,而EG6OH-SAMs通常抵抗蛋白质吸附,无论使用何种组装溶剂。

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