efficient antifouling surface for quantitative surface plasmon resonance based biosensor analysis有效的防污表面定量分析基于表面等离子体共振生物传感器.pdfVIP

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efficient antifouling surface for quantitative surface plasmon resonance based biosensor analysis有效的防污表面定量分析基于表面等离子体共振生物传感器.pdf

efficient antifouling surface for quantitative surface plasmon resonance based biosensor analysis有效的防污表面定量分析基于表面等离子体共振生物传感器

Efficient Antifouling Surface for Quantitative Surface Plasmon Resonance Based Biosensor Analysis 1 ´ 1 2 1 1 Claude Nogues , Herve Leh , Joseph Lautru , Olivier Delelis , Malcolm Buckle * 1 LBPA, ENS de Cachan, CNRS, Cachan, France, 2 Institut d’Alembert, ENS de Cachan, Cachan, France Abstract Non-specific binding to biosensor surfaces is a major obstacle to quantitative analysis of selective retention of analytes at immobilized target molecules. Although a range of chemical antifouling monolayers has been developed to address this problem, many macromolecular interactions still remain refractive to analysis due to the prevalent high degree of non- specific binding. In this manuscript we explore the dynamic process of the formation of self-assembled monolayers and optimize physical and chemical properties thus reducing considerably non-specific binding while maintaining the integrity of the immobilized biomolecules. As a result, analysis of specific binding of analytes to immobilized target molecules is significantly facilitated. Citation: Nogues C, Leh H, Lautru J, Delelis O, Buckle M (2012) Efficient Antifouling Surface for Quantitative Surface Plasmon Resonance Based Biosensor Analysis. PLoS ONE 7(9): e44287. doi:10.1371/journal.pone.0044287 Editor: Miklos S. Kellermayer, Semmelweis University, Hungary Received April 9, 2012; Accepted August 1, 2012; Published September 12, 2012 Copyright: 2012 Nogues et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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