Université Paris-Saclay, Institut d'Optique Graduate School, CNRS, Laboratoire Charles Fabry, Palaiseau, France.
Université Paris-Saclay, Institut des Sciences Moléculaires d'Orsay, CNRS, Centre de Photonique pour la Biologie et les Matériaux, Orsay, France.
J Biomed Opt. 2023 Aug;28(8):082808. doi: 10.1117/1.JBO.28.8.082808. Epub 2023 Jul 11.
Forces inside cells play a fundamental role in tissue growth, affecting important processes such as cancer cell migration or tissue repair after injury. Förster resonance energy transfer (FRET)-based tension sensors are a remarkable tool for studying these forces and should be made easier to use.
We prove that absolute FRET efficiency can be measured on a simple setup, an order of magnitude more cost-effective than a standard FRET microscopy setup, by applying it to vinculin tension sensors (VinTS) at the focal adhesions of live CHO-K1 cells.
Our setup located at Université Paris-Saclay acquires donor and acceptor fluorescence in parallel on two low-cost CMOS cameras and uses two LEDs for rapid switching of the excitation wavelength at a reduced cost. The calibration required to extract FRET efficiency was achieved using a single construct (TSMod). FRET efficiencies were measured for VinTS and the tail-less control VinTL, lacking the actin-binding domain of vinculin. Measurements were confirmed on the same cell type using a more standard intensity-based setup located at Rutgers University.
The average FRET efficiency of VinTS () over more than 10,000 focal adhesions is significantly lower () than that of VinTL (), our control that is insensitive to force, in agreement with the force exerted on vinculin at focal adhesions. Attachment of the CHO-K1 cells on fibronectin decreases FRET efficiency, thus increasing the force, compared with poly-lysine. FRET efficiency for the VinTL control is consistent with all measurements currently available in the literature, confirming the validity of our measurements and hence of our simpler setup.
Force measurements, resolved spatially inside a cell, can be achieved using FRET-based tension sensors with a cost effective intensity-based setup. This will facilitate combining FRET with techniques for applying controlled forces such as optical tweezers.
细胞内的力在组织生长中起着基本作用,影响着重要过程,如癌细胞迁移或受伤后的组织修复。基于Förster 共振能量转移(FRET)的张力传感器是研究这些力的一种极好的工具,应该使其更易于使用。
我们通过将其应用于活 CHO-K1 细胞的焦点黏附处的 vinculin 张力传感器(VinTS),证明了在简单的设置上可以测量绝对 FRET 效率,比标准 FRET 显微镜设置便宜一个数量级,该设置位于巴黎萨克雷大学。
我们的设置使用两个低成本 CMOS 相机并行获取供体和受体荧光,并使用两个 LED 以降低成本快速切换激发波长。为了从校准中提取 FRET 效率,我们使用了单个构建体(TSMod)。我们在同一细胞类型上使用更标准的基于强度的设置在罗格斯大学进行了确认,该设置测量了 VinTS 和缺乏 vinculin 肌动蛋白结合域的无尾对照 VinTL 的 FRET 效率。
超过 10000 个焦点黏附处的 VinTS 的平均 FRET 效率()明显低于力不敏感的 VinTL 对照物(),这与在焦点黏附处施加在 vinculin 上的力一致。与聚赖氨酸相比,CHO-K1 细胞在纤维连接蛋白上的附着会降低 FRET 效率,从而增加力。VinTL 对照物的 FRET 效率与目前文献中所有测量结果一致,证实了我们测量结果的有效性,从而也证实了我们更简单设置的有效性。
可以使用具有成本效益的基于强度的设置的基于 FRET 的张力传感器来实现细胞内空间分辨率的力测量。这将有助于将 FRET 与施加受控力的技术(如光学镊子)结合使用。