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High-speed atomic force microscopy combined with inverted optical microscopy for studying cellular events.

机译:高速原子力显微镜结合倒置光学显微镜用于研究细胞事件。

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摘要

A hybrid atomic force microscopy (AFM)-optical fluorescence microscopy is a powerful tool for investigating cellular morphologies and events. However, the slow data acquisition rates of the conventional AFM unit of the hybrid system limit the visualization of structural changes during cellular events. Therefore, high-speed AFM units equipped with an optical/fluorescence detection device have been a long-standing wish. Here we describe the implementation of high-speed AFM coupled with an optical fluorescence microscope. This was accomplished by developing a tip-scanning system, instead of a sample-scanning system, which operates on an inverted optical microscope. This novel device enabled the acquisition of high-speed AFM images of morphological changes in individual cells. Using this instrument, we conducted structural studies of living HeLa and 3T3 fibroblast cell surfaces. The improved time resolution allowed us to image dynamic cellular events.
机译:混合原子力显微镜(AFM)-光学荧光显微镜是研究细胞形态和事件的强大工具。然而,混合系统的常规AFM单元的缓慢的数据采集速率限制了细胞事件期间结构变化的可视化。因此,长期以来一直期望配备有光学/荧光检测装置的高速AFM单元。在这里,我们描述了结合光学荧光显微镜的高速原子力显微镜的实现。这是通过开发尖端扫描系统而不是在倒置光学显微镜上运行的样品扫描系统来完成的。这种新颖的设备能够采集单个细胞形态变化的高速AFM图像。使用该仪器,我们对HeLa和3T3成纤维细胞的活细胞表面进行了结构研究。改进的时间分辨率使我们能够对动态细胞事件进行成像。

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