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Wide-field subdiffraction imaging by accumulated binding of diffusing probes

机译:通过扩散探针的累积结合进行宽场亚衍射成像

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摘要

A method is introduced for subdiffraction imaging that accumulates points by collisional flux. It is based on targeting the surface of objects by fluorescent probes diffusing in the solution. Because the flux of probes at the object is essentially constant over long time periods, the examination of an almost unlimited number of individual probe molecules becomes possible. Each probe that hits the object and that becomes immobilized is located with high precision by replacing its point-spread function by a point at its centroid. Images of lipid bilayers, contours of these bilayers, and large unilamellar vesicles are shown. A spatial resolution of approximate to 25 nm is readily achieved. The ability of the method to effect rapid nanoscale imaging and spatial resolution below Rayleigh criterion and without the necessity for labeling with fluorescent probes is proven.
机译:介绍了一种用于子衍射成像的方法,该方法通过碰撞通量累积​​点。它基于在溶液中扩散的荧光探针对物体表面的瞄准。因为探针在物体上的通量在很长一段时间内基本恒定,所以检查几乎无限数量的单个探针分子成为可能。通过将质点的点替换为点扩展功能,可以精确定位击中对象并固定的每个探针。显示了脂质双层的图像,这些双层的轮廓以及大的单层囊泡。容易达到大约25 nm的空间分辨率。证明了该方法能够在瑞利标准之下实现快速的纳米级成像和空间分辨率,并且无需使用荧光探针标记的能力。

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