Földes-Papp Zeno
Medical University of Graz, Department of Internal Medicine, Riesstrasse 58a/5, A-8047 Graz, Austria.
Exp Mol Pathol. 2007 Apr;82(2):147-55. doi: 10.1016/j.yexmp.2006.12.002. Epub 2006 Dec 22.
Fluorescence correlation spectroscopy (FCS) and two-color fluorescence cross-correlation spectroscopy (FCCS) are a measure of fluctuations of detected light as a fluorescence molecule diffuses through a femtoliter detection volume caused by a tightly focused laser and confocal optics. Fluorescence from a single molecule can easily be distinguished from the slight background associated with a femtoliter of solvent. At a solution concentration of about 1 nM, the probability that there is an analyte molecule in the probe volume is less than one. Although fluorescence from individual molecules is collected, the data are analyzed by autocorrelation or two-color cross-correlation functions that are the average of thousands of molecules. Properties of single molecules are not obtained. I have been working on problems and opportunities associated with very dilute solutions. The molecule in the confocal probe volume is most probably the molecule that just diffused out, turned around, and diffused back in, i.e., reentered. For the first time, some theoretical results of the novel theory of the meaningful time are presented that enable study of just one single molecule over extended periods of times without immobilization or hydrodynamic focusing. Reentries that may also be called reoccurrences or encounters of a single molecule are significant because during measurement times they give rise to fluctuation phenomena such as molecule number fluctuations. Likewise, four criteria have been developed that can be used to verify that there is only one "selfsame" molecule in the laser probe volume during the experiment: (Földes-Papp, Z., 2006. What it means to measure a single molecule in a solution by fluorescence fluctuation spectroscopy. Exp. Mol. Pathol. 80 (3) 209-218).
荧光相关光谱法(FCS)和双色荧光交叉相关光谱法(FCCS)是一种测量检测光波动的方法,当荧光分子通过由紧密聚焦的激光和共焦光学系统产生的飞升检测体积扩散时,会产生这种波动。单个分子发出的荧光很容易与与飞升体积溶剂相关的微弱背景区分开来。在溶液浓度约为1 nM时,探针体积中存在分析物分子的概率小于1。虽然收集了单个分子的荧光,但数据是通过自相关或双色交叉相关函数进行分析的,这些函数是数千个分子的平均值。无法获得单个分子的特性。我一直在研究与极稀溶液相关的问题和机遇。共焦探针体积中的分子很可能是刚刚扩散出去、转身又扩散回来,即重新进入的分子。首次提出了有意义时间新理论的一些理论结果,该理论能够在不固定或流体动力学聚焦的情况下,长时间研究单个分子。单个分子的重新进入(也可称为重现或相遇)很重要,因为在测量期间它们会引发诸如分子数波动等波动现象。同样,已经制定了四个标准,可用于验证实验期间激光探针体积中是否只有一个“相同”分子:(Földes-Papp, Z., 2006. What it means to measure a single molecule in a solution by fluorescence fluctuation spectroscopy. Exp. Mol. Pathol. 80 (3) 209 - 218)。