Interests and limits of continuous excitation photo-physical methods applied to cellular rheology.

J C Andre, M Donner, M Bouchy, M L Viriot, J Y Jezequel, J F Stoltz
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Abstract

It is possible to characterize the cohesion of the lipidic zones in cells or in membranes by using molecular emission spectroscopy techniques such as : fluorescence polarization, quenching reactions, intramolecular reactions. However, applying these techniques in biology can be improved by the use of pulsed excitations leading to the time-resolved evolutions of some properties of the probe, which can themselves be a function of their environment. The first and the last techniques, based on the use of diphenylhexatriene and dipyrenylpropane respectively are used in practice by steady state excitation. In the case of fluorescence polarization, it can be shown that the method can be applied, within certain limits, which have to be precised when studying the modifications in the membranes. This is also partly true for methods based on the use of intramolecular reactions. However these continuous excitation techniques usually only lead to a global result which is a function of several spectroscopic parameters and of the "cohesion" of the membrane. Then it can be shown that to go beyond this step of semi-quantitative analysis, it is necessary to use pulsed or modulated excitation methods. Moreover this more sophisticated technical approach implies a new theoretical effort to understand the molecular dynamics of the membranes.

应用于细胞流变学的连续激发光物理方法的兴趣和局限性。
利用分子发射光谱技术,如荧光极化、猝灭反应、分子内反应,可以表征细胞或膜中脂质带的内聚性。然而,在生物学中应用这些技术可以通过使用脉冲激发来改进探针的一些特性的时间分辨进化,这些特性本身可以是它们的环境的函数。第一种技术和最后一种技术分别以二苯基己三烯和二苯基丙烷为原料,通过稳态激励在实践中得到了应用。在荧光极化的情况下,可以表明该方法可以在一定范围内应用,在研究膜中的修饰时必须精确。这在一定程度上也适用于基于分子内反应的方法。然而,这些连续激发技术通常只能得到一个全局的结果,这个结果是几个光谱参数和膜的“凝聚力”的函数。然后可以证明,要超越半定量分析的这一步,有必要使用脉冲或调制激励方法。此外,这种更复杂的技术方法意味着一种新的理论努力来理解膜的分子动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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