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用于横向扩散的衍射极限测量的线扫描显微光解技术。

Line-scanning microphotolysis for diffraction-limited measurements of lateral diffusion.

作者信息

Wedekind P, Kubitscheck U, Heinrich O, Peters R

机构信息

Institut für Medizinische Physik und Biophysik, Westfälische Wilhelms-Universität, Münster, Germany.

出版信息

Biophys J. 1996 Sep;71(3):1621-32. doi: 10.1016/S0006-3495(96)79366-9.

Abstract

Fluorescence microphotolysis was combined with confocal laser-scanning microscopy to yield a method, herein referred to as line-scanning microphotolysis (LINESCAMP), for the measurement of molecular transport at a lateral resolution of approximately 0.34 microns and a temporal resolution of approximately 0.5 ms. A confocal microscope was operated in the line scan mode, while the laser beam power could be switched during scanning between low monitoring and high photolysing levels in less then a microsecond. The number and location of line segments to be photolysed could be freely determined. The length of the photolysed segments could be also chosen and was only limited by diffraction. Together with instrumentation a new, completely general, theoretical framework for the evaluation of diffusion measurements was developed. Based on the numerical simulation of diffusion processes employing a modified Crank-Nicholson scheme, the theory could be applied to any photobleaching geometry and profile as the initial condition and took into account the convolution with the microscope point spread function. With small diffraction-limited areas, the method yielded accurate values for diffusion coefficients in the range between approximately 10(-4) and 1 micron2 s-1. A first application of the method to the diffusion of a fluorescently labeled tracer inside the cell nucleus showed the potential of the method for the study of complex biological systems.

摘要

荧光显微光解技术与共聚焦激光扫描显微镜相结合,产生了一种在此称为线扫描显微光解(LINESCAMP)的方法,用于在横向分辨率约为0.34微米和时间分辨率约为0.5毫秒的条件下测量分子运输。共聚焦显微镜在线扫描模式下运行,同时激光束功率可在扫描期间在不到一微秒的时间内从低监测水平切换到高光解水平。待光解的线段数量和位置可自由确定。光解线段的长度也可以选择,并且仅受衍射限制。连同仪器一起,还开发了一个全新的、完全通用的用于评估扩散测量的理论框架。基于采用改进的克兰克-尼科尔森格式对扩散过程进行的数值模拟,该理论可应用于任何光漂白几何形状和轮廓作为初始条件,并考虑了与显微镜点扩散函数的卷积。对于小的衍射极限区域,该方法可得出约10^(-4)至1微米^2·秒^(-1)范围内扩散系数的准确值。该方法首次应用于细胞核内荧光标记示踪剂的扩散,显示了该方法在研究复杂生物系统方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c29/1233630/e73f57026eb6/biophysj00043-0462-a.jpg

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