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Near-field optical probes provide subdiffraction-limited excitation areas for fluorescence correlation spectroscopy on membranes

机译:近场光学探针为膜上的荧光相关光谱提供了亚衍射限制的激发区域

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摘要

Near-field optical probes have been used to produce a subdiffraction-limited observation area for fluorescence correlation spectroscopy (FCS) experiments on supported membranes. The design of a bent, etched fiber probe that is compatible with biological imaging in an aqueous environment is described. This probe design is used for proof of principle experiments to measure lipid diffusion in a fluid-supported bilayer. A reduction in excitation area of approximately one order of magnitude (relative to a confocal FCS experiment) is obtained with a probe aperture diameter of 140 nm. We also demonstrate a simple approach for modeling the autocorrelation decay due to diffusion within the excitation profile at the near-field scanning optical microscopy (NSOM) probe aperture. The use of probes with smaller apertures is expected to provide an additional order of magnitude reduction in the observation area, thus enabling the study of cellular membranes with higher concentrations of fluorophores than is currently possible with diffraction-limited techniques.
机译:近场光学探针已被用于产生亚衍射极限的观察区域,用于在支持膜上进行荧光相关光谱(FCS)实验。描述了一种弯曲的蚀刻纤维探针的设计,该探针与水性环境中的生物成像兼容。该探针设计用于原理实验的证明,以测量脂质在流体支撑双层中的扩散。探针孔径为140 nm时,激发面积减少了大约一个数量级(相对于共焦FCS实验)。我们还展示了一种简单的方法,可用于建模由于在近场扫描光学显微镜(NSOM)探头孔径处的激发轮廓内的扩散而引起的自相关衰减。期望使用具有较小孔径的探针可以在观察区域中提供一个额外的数量级减少,从而使得与目前的衍射极限技术相比,能够研究具有更高浓度的荧光团的细胞膜。

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