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Ultrasensitive Plasmonic Platform for Label-Free Detection of Membrane-Associated Species

机译:超灵敏的等离子平台,用于膜相关物种的无标签检测。

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摘要

Lipid membranes and membrane proteins are important biosensing targets, motivating the development of label-free methods with improved sensitivity. Silica-coated metal nanoparticles allow these systems to be combined with supported lipid bilayers for sensing membrane proteins through localized surface plasmon resonance (LSPR). However, the small sensing volume of LSPR makes the thickness of the silica layer critical for performance. Here, we develop a simple, inexpensive, and rapid sol gel method for preparing thin conformal, continuous silica films and demonstrate its applicability using gold nanodisk arrays with LSPRs in the near-infrared range. Silica layers as thin as nm are observed using cross-sectional scanning transmission electron microscopy. The loss in sensitivity due to the thin silica coating was found to be only 16%, and the biosensing capabilities of the substrates were assessed through the binding of cholera toxin B to GM1 lipids. This sensor platform should prove useful in the rapid, multiplexed detection and screening of membrane-associated biological targets.
机译:脂质膜和膜蛋白是重要的生物传感靶标,从而促进了无标记方法的开发,并提高了灵敏度。二氧化硅涂层的金属纳米颗粒使这些系统可以与支持的脂质双层结合,以通过局部表面等离子体共振(LSPR)感测膜蛋白。但是,LSPR的检测体积较小,因此二氧化硅层的厚度对于性能至关重要。在这里,我们开发了一种简单,便宜且快速的溶胶凝胶方法,用于制备薄的保形连续二氧化硅薄膜,并证明了使用具有近红外范围内LSPR的金纳米盘阵列的适用性。使用截面扫描透射电子显微镜观察到的二氧化硅层薄至nm。发现由于二氧化硅薄涂层导致的灵敏度损失仅为16%,并且通过霍乱毒素B与GM1脂质的结合来评估底物的生物传感能力。该传感器平台应被证明可用于快速,多重检测和筛选膜相关生物靶标。

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