Laboratory of Physical Chemistry of Polymers and Membranes, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland.
Nano Lett. 2012 Jan 11;12(1):370-5. doi: 10.1021/nl2036468. Epub 2011 Dec 12.
A central goal in bioanalytics is to determine the concentration of and interactions between biomolecules. Nanotechnology allows performing such analyses in a highly parallel, low-cost, and miniaturized fashion. Here we report on label-free volume, concentration, and mobility analysis of single protein molecules and nanoparticles during their diffusion through a subattoliter detection volume, confined by a 100 nm aperture in a thin gold film. A high concentration of small fluorescent molecules renders the aqueous solution in the aperture brightly fluorescent. Nonfluorescent analytes diffusing into the aperture displace the fluorescent molecules in the solution, leading to a decrease of the detected fluorescence signal, while analytes diffusing out of the aperture return the fluorescence level. The resulting fluorescence fluctuations provide direct information on the volume, concentration, and mobility of the nonfluorescent analytes through fluctuation analysis in both time and amplitude.
生物分析的一个核心目标是确定生物分子的浓度和相互作用。纳米技术允许以高度并行、低成本和微型化的方式进行此类分析。在这里,我们报告了在通过薄金膜中的 100nm 孔径进行亚皮升检测体积时,单个蛋白质分子和纳米颗粒在扩散过程中的无标记体积、浓度和迁移率分析。高浓度的小荧光分子使孔径中的水溶液呈现明亮的荧光。扩散到孔径中的非荧光分析物会取代溶液中的荧光分子,导致检测到的荧光信号减弱,而从孔径中扩散出来的分析物则会使荧光水平恢复。由此产生的荧光波动通过在时间和幅度上进行波动分析,为非荧光分析物的体积、浓度和迁移率提供了直接信息。