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一种基于等离子体激活的快速且可重现的硅烷化方法,用于基于疏水性的驱动蛋白单分子荧光显微镜检测。

A Quick and Reproducible Silanization Method by Using Plasma Activation for Hydrophobicity-Based Kinesin Single Molecule Fluorescence-Microscopy Assays.

机构信息

Eberhard Karls Universität Tübingen, Cellular Nanoscience (ZMBP), Auf der Morgenstelle 32, 72076, Tübingen, Germany.

Eberhard Karls Universität Tübingen, Institute of Physical and Theoretical Chemistry, Auf der Morgenstelle 18, 72076, Tübingen, Germany.

出版信息

Chemistry. 2022 Nov 16;28(64):e202202036. doi: 10.1002/chem.202202036. Epub 2022 Sep 14.

Abstract

Single-molecule assays often require functionalized surfaces. One approach for microtubule assays renders surfaces hydrophobic and uses amphiphilic blocking agents. However, the optimal hydrophobicity is unclear, protocols take long, produce toxic waste, and are susceptible to failure. Our method uses plasma activation with hydrocarbons for hexamethyldisilazane (HMDS) silanization in the gas phase. We measured the surface hydrophobicity, its effect on how well microtubule filaments were bound to the surface, and the number of nonspecific interactions with kinesin motor proteins. Additionally, we tested and discuss the use of different silanes and activation methods. We found that even weakly hydrophobic surfaces were optimal. Our environmentally friendly method significanty reduced the overall preparation effort and resulted in reproducible, high-quality surfaces with low variability. We expect the method to be applicable to a wide range of other single-molecule assays.

摘要

单细胞分析实验通常需要功能化的表面。一种微管分析方法是使表面疏水并用两亲性封闭剂处理。然而,最优的疏水性并不明确,该方法耗时、产生有毒废物且容易失败。我们的方法使用烃类物质对六甲基二硅氮烷(HMDS)进行气相等离子体激活硅烷化。我们测量了表面疏水性、它对微管丝与表面结合程度的影响,以及与驱动蛋白马达蛋白的非特异性相互作用的数量。此外,我们还测试和讨论了不同硅烷和激活方法的使用。我们发现,即使是弱疏水性的表面也是最佳的。我们的环保方法大大减少了整体准备工作,并产生了具有低变异性的可重现、高质量的表面。我们预计该方法将适用于广泛的其他单细胞分析实验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78e7/9826530/718af40734e4/CHEM-28-0-g002.jpg

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