Department of Physical Chemistry, University of Geneva, 1211 Geneva, Switzerland.
Department of Inorganic and Analytical Chemistry, University of Geneva, 1211 Geneva, Switzerland.
J Phys Chem B. 2024 Aug 22;128(33):7997-8006. doi: 10.1021/acs.jpcb.4c02506. Epub 2024 Aug 9.
A milestone in optical imaging of mechanical forces in cells has been the development of the family of flipper fluorescent probes able to report membrane tension noninvasively in living cells through their fluorescence lifetime. The specifically designed Flipper-CF probe with an engineered inherent blinking mechanism was recently introduced for super-resolution fluorescence microscopy of lipid ordered membranes but was too dim to be detected in lipid disordered membranes at the single-molecule level (García-Calvo, J. 2020, 142(28), 12034-12038). We show here that the original and commercially available probe Flipper-TR is compatible with single-molecule based super-resolution imaging and resolves both liquid ordered and liquid disordered membranes of giant unilamellar vesicles below the diffraction limit. Single probe molecules were additionally tracked in lipid bilayers, enabling to distinguish membranes of varying composition from the diffusion coefficient of the probe. Differences in brightness between Flipper-CF and Flipper-TR originate in their steady-state absorption and fluorescence properties. The general compatibility of the Flipper-TR scaffold with single-molecule detection is further shown in super-resolution experiments with targetable Flipper-TR derivatives.
光学成像技术在细胞力学研究方面取得了重要进展,其中 flipper 荧光探针家族的发展引人注目。该探针家族能够通过荧光寿命非侵入式地报告活细胞中的膜张力。最近,一款具有工程化固有闪烁机制的专门设计的 Flipper-CF 探针被引入到脂质有序膜的超分辨率荧光显微镜中,但由于其荧光强度太弱,无法在脂质无序膜中单分子水平上检测到(García-Calvo, J. 2020, 142(28), 12034-12038)。我们在这里表明,原始的和市售的 Flipper-TR 探针与基于单分子的超分辨率成像兼容,并在低于衍射极限的情况下解析大单层囊泡的液体有序和液体无序膜。此外,我们还可以在脂质双层中单探针分子进行跟踪,从而能够根据探针的扩散系数来区分不同组成的膜。Flipper-CF 和 Flipper-TR 之间的亮度差异源于它们的稳态吸收和荧光特性。靶向 Flipper-TR 衍生物的超分辨率实验进一步证明了 Flipper-TR 支架与单分子检测的普遍兼容性。