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Transfected Single-Cell Imaging by Scanning Electrochemical Optical Microscopy with Shear Force Feedback Regulation

机译:扫描电化学光学显微镜与剪切力反馈调节转染的单细胞成像。

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摘要

Gene-transfected single HeLa cells were characterized using a scanning electrochemical/optical microscope (SECM/OM) system with shear-force-based probe-sample distance regulation to simultaneously capture electrochemical, fluorescent, and topographic images. The outer and inner states of single living cells were obtained as electrochemical and fluorescent signals, respectively, by using an optical fiber-nanoelectrode probe. A focused ion beam (FIB) was used to mill the optical aperture and the ring electrode at the probe apex (the inner and outer radii of the ring electrode were 37 and 112 nm, respectively). To apply an appropriate shear force between the probe tip and the living cell surface, we optimized the amplitude of oscillation of the tuning fork to which the probe was attached. Field-programmable gate arrays (FPGA) were adopted to drastically increase the feedback speed of the tip-sample distance regulation, shorten the scanning time for imaging, and enhance the accuracy and quality of the living cell images. In employing these improvements, we simultaneously measured the cellular expression activity of both secreted alkaline phosphatase outside and GFP inside by using the SECM/OM with shear force distance regulation.
机译:基因转染的单个HeLa细胞使用扫描电化学/光学显微镜(SECM / OM)系统进行表征,该系统具有基于剪切力的探针-样品距离调节功能,可同时捕获电化学,荧光和地形图图像。使用光纤-纳米电极探针分别获得单个活细胞的外部和内部状态作为电化学和荧光信号。使用聚焦离子束(FIB)研磨探针顶部的光学孔径和环形电极(环形电极的内半径和外半径分别为37 nm和112 nm)。为了在探针尖端和活细胞表面之间施加适当的剪切力,我们优化了连接探针的音叉的振幅。采用现场可编程门阵列(FPGA)可以大大提高尖端样品距离调节的反馈速度,缩短成像的扫描时间,并提高活细胞图像的准确性和质量。通过采用这些改进,我们通过使用具有剪切力距离调节功能的SECM / OM同时测量了外部分泌的碱性磷酸酶和GFP内部的细胞表达活性。

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