Bastos André E P, Scolari Silvia, Stöckl Martin, Almeida Rodrigo F M de
Centro de Química e Bioquímica, Faculdade de Ciências da Universidade de Lisboa, Lisboa, Portugal.
Methods Enzymol. 2012;504:57-81. doi: 10.1016/B978-0-12-391857-4.00003-3.
Lipid domains are part of the current description of cell membranes and their involvement in many fundamental cellular processes is currently acknowledged. However, their study in living cells is still a challenge. Fluorescence lifetimes have and will continue to play an important role in unraveling the properties and function of lipid domains, and their use in vivo is expected to increase in the near future, since their extreme sensitivity to the physical properties of the membrane and the possibility of optical imaging are particularly suited to deal with the hurdles that are met by researchers. In this review, a practical guide on the use of fluorescence lifetimes for the study of this subject is given. A section is devoted to studies in vitro, particularly membrane model systems, and how they are used to better design and correctly interpret results obtained in living cells. Criteria are presented for selecting suitable probes to solve each problem, drawing attention to factors sometimes overlooked and which may affect the fluorescence lifetime such as subcellular distribution and concentration of the probe. The principal groups of lifetime probes for lipid domains: (i) fluorescent lipid analogues, (ii) other lipophilic probes, and (iii) fluorescent proteins, and respective applications are briefly described and lab tips about the labeling of living cells are provided. The advantages and complementarities of spectroscopy (cuvette) work and fluorescence lifetime imaging microscopy are presented and illustrated with three selected case studies: (i) the finding of a new type of lipid rafts in yeast cells; (ii) the detection of liquid ordered type heterogeneity in animal cells below optical resolution; and (iii) establish a role for the transmembrane domain of influenza virus hemagglutinin with cholesterol-enriched domains in mammalian cells.
脂类结构域是目前细胞膜描述的一部分,并且它们在许多基本细胞过程中的参与目前已得到认可。然而,在活细胞中对其进行研究仍然是一项挑战。荧光寿命已经并将继续在揭示脂类结构域的性质和功能方面发挥重要作用,并且由于其对膜物理性质的极端敏感性以及光学成像的可能性特别适合应对研究人员所遇到的障碍,预计在不久的将来其在体内的应用将会增加。在这篇综述中,给出了一份关于使用荧光寿命研究该主题的实用指南。有一部分专门介绍了体外研究,特别是膜模型系统,以及它们如何用于更好地设计和正确解释在活细胞中获得的结果。提出了选择合适探针以解决每个问题的标准,提请注意有时被忽视且可能影响荧光寿命的因素,如探针的亚细胞分布和浓度。简要描述了用于脂类结构域的主要寿命探针组:(i)荧光脂质类似物,(ii)其他亲脂性探针,以及(iii)荧光蛋白,并提供了关于活细胞标记的实验提示。介绍了光谱学(比色皿)工作和荧光寿命成像显微镜的优点和互补性,并通过三个选定的案例研究进行说明:(i)在酵母细胞中发现一种新型脂筏;(ii)在低于光学分辨率的动物细胞中检测液态有序型异质性;以及(iii)确定流感病毒血凝素跨膜结构域在哺乳动物细胞中与富含胆固醇的结构域的作用。