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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Modified Pluronic F127 Surface for Bioconjugation and Blocking Nonspecific Adsorption of Microspheres and Biomacromolecules
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Modified Pluronic F127 Surface for Bioconjugation and Blocking Nonspecific Adsorption of Microspheres and Biomacromolecules

机译:用于生物缀合物的改进的Pluronic F127表面并阻断微球和生物致摩托的非特异性吸附

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摘要

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.
机译:许多实验和应用需要靶分子与表面的化学偶联,在此期间消除非特异性相互作用呈现困难的挑战。我们报告了基于NHS末端标记的F127 Pluronic嵌段共聚物(F127-NHS)的技术可接近的表面钝化和化学缀合方法。为了量化F127-NHS表面和磁性微球之间的相互作用,我们开发了一种简单的测定:通过重力,反转,然后计数或“魔法”测定的微球粘附。为了改善微球的阻断,同时保持化学耦合额外分子的能力,我们实施了胺微球的pH依赖性两步化学改性方法。该方法实现了各种微球表面电荷和化学功能的极高含量阻断非特异性相互作用(小于2%的非特异性粘附)。我们还证明了使用单个DNA分子将磁性微球特异性磁性微球体特异性的能力。使用DNA微球,我们通过聚离心机显微镜显微镜的大规模平行技术建立表面的适用性(用施加的负载& 30 pn)。最后,我们证明该表面可以用于荧光研究的荧光肽裂解测定,对荧光肽和胰蛋白酶达到高水平的阻断。这些结果表明应用包括但不限于单分子力光谱和荧光,生物传感器,医疗植入物和抗生物污染,这可以利用F127-NHS表面。

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