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改性 Pluronic F127 表面用于微球和生物大分子的生物缀合和阻止非特异性吸附。

Modified Pluronic F127 Surface for Bioconjugation and Blocking Nonspecific Adsorption of Microspheres and Biomacromolecules.

出版信息

Langmuir. 2018 Nov 13;34(45):13550-13557. doi: 10.1021/acs.langmuir.8b02877. Epub 2018 Oct 29.

DOI:10.1021/acs.langmuir.8b02877
PMID:30303387
Abstract

Many experiments and applications require the chemical coupling of target molecules to surfaces, during which the elimination of nonspecific interactions presents a difficult challenge. We report on a technologically accessible surface passivation and chemical conjugation method based on an NHS end-labeled F127 Pluronic block copolymer (F127-NHS). To quantify interactions between the F127-NHS surface and magnetic microspheres, we developed a simple assay: the microsphere adhesion by gravity, inversion, then counting, or "MAGIC" assay. To improve blocking of microspheres while maintaining the ability to chemically couple additional molecules, we implemented a pH-dependent two-step chemical modification process for amine microspheres. This process achieves an extremely high level of blocking nonspecific interactions (less than 2% nonspecific adhesion) for a variety of microsphere surface charges and chemical functionalities. We also demonstrate the ability to specifically tether magnetic microspheres to an F127-NHS surface, using single DNA molecules. Using the DNA microspheres, we establish the applicability of the surface for force spectroscopy (stable with an applied load >30 pN) via the massively parallel technique of centrifuge force microscopy. Finally, we demonstrate that the surface can be used in fluorescence studies with a fluorogenic peptide cleavage assay, with high levels of blocking achieved for both the fluorogenic peptide and trypsin. These results suggest applications including, but not limited to, single-molecule force spectroscopy and fluorescence, biosensors, medical implants, and anti-biofouling, which could make use of the F127-NHS surface.

摘要

许多实验和应用都需要将目标分子化学偶联到表面,在此过程中,消除非特异性相互作用是一个具有挑战性的问题。我们报告了一种基于 NHS 末端标记的 F127 嵌段共聚物(F127-NHS)的技术上可实现的表面钝化和化学偶联方法。为了量化 F127-NHS 表面与磁性微球之间的相互作用,我们开发了一种简单的测定方法:通过重力、倒置和计数使微球附着,或称为“MAGIC”测定法。为了在保持化学偶联其他分子能力的同时改善微球的阻断效果,我们对胺基微球实施了 pH 依赖性两步化学修饰过程。该过程可实现各种微球表面电荷和化学功能的极高水平的阻断非特异性相互作用(非特异性附着率小于 2%)。我们还展示了使用单链 DNA 分子将磁性微球特异性地固定到 F127-NHS 表面的能力。使用 DNA 微球,我们通过离心力显微镜的大规模并行技术建立了表面适用于力谱学(在超过 30 pN 的施加负载下稳定)的适用性。最后,我们证明该表面可用于荧光研究,使用荧光肽切割测定法实现了对荧光肽和胰蛋白酶的高阻断效果。这些结果表明了一些应用的可能性,包括但不限于单分子力谱学和荧光、生物传感器、医疗植入物和抗生物污染,这些应用都可以利用 F127-NHS 表面。

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