School of Chemistry and Biochemistry and ‡National Centre of Competence in Research (NCCR) Chemical Biology , University of Geneva , CH-1211 Geneva , Switzerland.
J Am Chem Soc. 2019 Feb 27;141(8):3380-3384. doi: 10.1021/jacs.8b13189. Epub 2019 Feb 12.
Measuring forces inside cells is particularly challenging. With the development of quantitative microscopy, fluorophores which allow the measurement of forces became highly desirable. We have previously introduced a mechanosensitive flipper probe, which responds to the change of plasma membrane tension by changing its fluorescence lifetime and thus allows tension imaging by FLIM. Herein, we describe the design, synthesis, and evaluation of flipper probes that selectively label intracellular organelles, i.e., lysosomes, mitochondria, and the endoplasmic reticulum. The probes respond uniformly to osmotic shocks applied extracellularly, thus confirming sensitivity toward changes in membrane tension. At rest, different lifetimes found for different organelles relate to known differences in membrane organization rather than membrane tension and allow colabeling in the same cells. At the organelle scale, lifetime heterogeneity provides unprecedented insights on ER tubules and sheets, and nuclear membranes. Examples on endosomal trafficking or increase of tension at mitochondrial constriction sites outline the potential of intracellularly targeted fluorescent tension probes to address essential questions that were previously beyond reach.
测量细胞内的力特别具有挑战性。随着定量显微镜技术的发展,能够测量力的荧光染料变得非常需要。我们之前介绍了一种机械敏感的翻转探针,它通过改变荧光寿命来响应质膜张力的变化,从而允许通过 FLIM 进行张力成像。本文描述了设计、合成和评估翻转探针的方法,这些探针可以选择性地标记细胞内的细胞器,即溶酶体、线粒体和内质网。这些探针对外界施加的渗透压冲击反应均匀,从而证实了它们对膜张力变化的敏感性。在静止状态下,不同细胞器的不同寿命与已知的膜组织差异有关,而不是与膜张力有关,这使得在同一细胞中进行共标记成为可能。在细胞器尺度上,寿命异质性为内质网小管和片层以及核膜提供了前所未有的见解。关于内体运输或线粒体收缩部位张力增加的例子,概述了针对细胞内靶向荧光张力探针的潜力,可以解决以前无法解决的基本问题。