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FCS细胞表面测量——光物理限制及其对具有异质迁移率的分子聚集体的影响。

FCS cell surface measurements--photophysical limitations and consequences on molecular ensembles with heterogenic mobilities.

作者信息

Widengren Jerker, Thyberg Per

机构信息

Department of Physics, Division of Experimental Biomolecular Physics, Royal Institute of Technology, Albanova University Center, 10691 Stockholm, Sweden.

出版信息

Cytometry A. 2005 Dec;68(2):101-12. doi: 10.1002/cyto.a.20193.

Abstract

BACKGROUND

Fluorescence Correlation Spectroscopy is a powerful method to analyze densities and diffusive behavior of molecules in membranes, but effects of photodegradation can easily be overlooked.

METHOD

Based on experimental photophysical parameters, calculations were performed to analyze the consequences of photobleaching in fluorescence correlation spectroscopy (FCS) cell surface experiments, covering a range of standard measurement conditions.

RESULTS

Cumulative effects of photobleaching can be prominent, although an absolute majority of the fluorescent molecules would pass the laser excitation beam without being photo-bleached. Given a distribution of molecules on a cell surface with different diffusive properties, the fraction of molecules that is actually analyzed depends strongly on the excitation intensities and measurement times, as well as on the size of the reservoir of freely diffusing molecules. Both the slower and the faster diffusing molecules can be disfavored.

CONCLUSIONS

Apart from quantifying photobleaching effects, the calculations suggest that the effects can be used to extract additional information, for instance about the size of the reservoirs of free diffusion. By certain choices of measurement conditions, it may be possible to more specifically analyze certain species within a population, based on their different diffusive properties, different areas of free diffusion, or different kinetics of possible transient binding.

摘要

背景

荧光相关光谱法是分析膜中分子密度和扩散行为的有力方法,但光降解的影响很容易被忽视。

方法

基于实验光物理参数进行计算,以分析荧光相关光谱法(FCS)细胞表面实验中光漂白的后果,涵盖一系列标准测量条件。

结果

尽管绝大多数荧光分子会在不被光漂白的情况下通过激光激发光束,但光漂白的累积效应可能很显著。对于细胞表面具有不同扩散特性的分子分布,实际分析的分子比例强烈取决于激发强度和测量时间,以及自由扩散分子库的大小。扩散较慢和较快的分子都可能受到不利影响。

结论

除了量化光漂白效应外,计算结果表明这些效应可用于提取额外信息,例如关于自由扩散库的大小。通过特定的测量条件选择,基于群体中某些物种不同的扩散特性、不同的自由扩散区域或可能的瞬时结合的不同动力学,有可能更具体地分析这些物种。

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