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用于单分子蛋白质研究的表面钝化

Surface passivation for single-molecule protein studies.

作者信息

Chandradoss Stanley D, Haagsma Anna C, Lee Young Kwang, Hwang Jae-Ho, Nam Jwa-Min, Joo Chirlmin

机构信息

Kavli Institute of NanoScience, Department of BioNanoScience, Delft University of Technology.

Department of Chemistry, Seoul National University.

出版信息

J Vis Exp. 2014 Apr 24(86):50549. doi: 10.3791/50549.

DOI:10.3791/50549
PMID:24797261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4179479/
Abstract

Single-molecule fluorescence spectroscopy has proven to be instrumental in understanding a wide range of biological phenomena at the nanoscale. Important examples of what this technique can yield to biological sciences are the mechanistic insights on protein-protein and protein-nucleic acid interactions. When interactions of proteins are probed at the single-molecule level, the proteins or their substrates are often immobilized on a glass surface, which allows for a long-term observation. This immobilization scheme may introduce unwanted surface artifacts. Therefore, it is essential to passivate the glass surface to make it inert. Surface coating using polyethylene glycol (PEG) stands out for its high performance in preventing proteins from non-specifically interacting with a glass surface. However, the polymer coating procedure is difficult, due to the complication arising from a series of surface treatments and the stringent requirement that a surface needs to be free of any fluorescent molecules at the end of the procedure. Here, we provide a robust protocol with step-by-step instructions. It covers surface cleaning including piranha etching, surface functionalization with amine groups, and finally PEG coating. To obtain a high density of a PEG layer, we introduce a new strategy of treating the surface with PEG molecules over two rounds, which remarkably improves the quality of passivation. We provide representative results as well as practical advice for each critical step so that anyone can achieve the high quality surface passivation.

摘要

单分子荧光光谱已被证明在理解纳米尺度上的各种生物现象方面发挥了重要作用。该技术对生物科学的重要贡献包括对蛋白质 - 蛋白质和蛋白质 - 核酸相互作用的机制性见解。当在单分子水平探测蛋白质相互作用时,蛋白质或其底物通常固定在玻璃表面,这便于进行长期观察。这种固定方案可能会引入不需要的表面伪影。因此,使玻璃表面钝化以使其呈惰性至关重要。使用聚乙二醇(PEG)进行表面涂层在防止蛋白质与玻璃表面非特异性相互作用方面表现出色。然而,聚合物涂层过程很困难,这是由于一系列表面处理带来的复杂性以及该过程结束时表面需要不含任何荧光分子的严格要求。在此,我们提供了一个详细的操作方案及分步说明。它涵盖了表面清洁,包括硫酸 - 过氧化氢混合溶液蚀刻、用胺基进行表面功能化,最后是PEG涂层。为了获得高密度的PEG层,我们引入了一种用PEG分子对表面进行两轮处理的新策略,这显著提高了钝化质量。我们为每个关键步骤提供了代表性结果以及实用建议,以便任何人都能实现高质量的表面钝化。

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