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用于测量液/固界面快速表面扩散的成像荧光相关光谱法。

Imaging fluorescence-correlation spectroscopy for measuring fast surface diffusion at liquid/solid interfaces.

作者信息

Cooper Justin T, Harris Joel M

机构信息

Department of Chemistry, University of Utah , 315 South 1400 East, Salt Lake City, Utah 84112-0805, United States.

出版信息

Anal Chem. 2014 Aug 5;86(15):7618-26. doi: 10.1021/ac5014354. Epub 2014 Jul 9.

Abstract

The development of techniques to probe interfacial molecular transport is important for understanding and optimizing surface-based analytical methods including surface-enhanced spectroscopies, biological assays, and chemical separations. Single-molecule-fluorescence imaging and tracking has been used to measure lateral diffusion rates of fluorescent molecules at surfaces, but the technique is limited to the study of slower diffusion, where molecules must remain relatively stationary during acquisition of an image in order to build up sufficient intensity in a spot to detect and localize the molecule. Although faster time resolution can be achieved by fluorescence-correlation spectroscopy (FCS), where intensity fluctuations in a small spot are related to the motions of molecules on the surface, long-lived adsorption events arising from surface inhomogeneity can overwhelm the correlation measurement and mask the surface diffusion of the moving population. Here, we exploit a combination of these two techniques, imaging-FCS, for measurement of fast interfacial transport at a model chromatographic surface. This is accomplished by rapid imaging of the surface using an electron-multiplied-charged-coupled-device (CCD) camera, while limiting the acquisition to a small area on the camera to allow fast framing rates. The total intensity from the sampled region is autocorrelated to determine surface diffusion rates of molecules with millisecond time resolution. The technique allows electronic control over the acquisition region, which can be used to avoid strong adsorption sites and thus minimize their contribution to the measured autocorrelation decay and to vary the acquisition area to resolve surface diffusion from adsorption and desorption kinetics. As proof of concept, imaging-FCS was used to measure surface diffusion rates, interfacial populations, and adsorption-desorption rates of 1,1'-dioctadecyl-3,3,3'3'-tetramethylindocarbocyanine (DiI) on planar C18- and C1-modified surfaces.

摘要

开发探测界面分子传输的技术对于理解和优化基于表面的分析方法(包括表面增强光谱学、生物测定和化学分离)至关重要。单分子荧光成像和跟踪已被用于测量荧光分子在表面的横向扩散速率,但该技术仅限于研究较慢的扩散,在这种情况下,分子在图像采集过程中必须保持相对静止,以便在一个点上积累足够的强度来检测和定位分子。虽然通过荧光相关光谱法(FCS)可以实现更快的时间分辨率,其中小光斑中的强度波动与表面分子的运动相关,但表面不均匀性引起的长寿命吸附事件会使相关测量不堪重负,并掩盖移动群体的表面扩散。在这里,我们利用这两种技术的组合,即成像FCS,来测量模型色谱表面的快速界面传输。这是通过使用电子倍增电荷耦合器件(CCD)相机对表面进行快速成像来实现的,同时将采集限制在相机上的一个小区域,以实现快速帧率。对采样区域的总强度进行自相关,以确定具有毫秒时间分辨率的分子表面扩散速率。该技术允许对采集区域进行电子控制,可用于避免强吸附位点,从而将其对测量的自相关衰减的贡献降至最低,并改变采集区域以从吸附和解吸动力学中解析表面扩散。作为概念验证,成像FCS被用于测量1,1'-二辛基-3,3,3'3'-四甲基吲哚碳菁(DiI)在平面C18和C1修饰表面上的表面扩散速率、界面群体以及吸附-解吸速率。

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