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A high speed multifocal multiphoton fluorescence lifetime imaging microscope for live-cell FRET imaging

机译:用于活细胞FRET成像的高速多焦点多光子荧光寿命成像显微镜

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We demonstrate diffraction limited multiphoton imaging in a massively parallel, fully addressable time-resolved multi-beam multiphoton microscope capable of producing fluorescence lifetime images with sub-50ps temporal resolution. This imaging platform offers a significant improvement in acquisition speed over single-beam laser scanning FLIM by a factor of 64 without compromising in either the temporal or spatial resolutions of the system. We demonstrate FLIM acquisition at 500 ms with live cells expressing green fluorescent protein. The applicability of the technique to imaging protein-protein interactions in live cells is exemplified by observation of time-dependent FRET between the epidermal growth factor receptor (EGFR) and the adapter protein Grb2 following stimulation with the receptor ligand. Furthermore, ligand-dependent association of HER2-HER3 receptor tyrosine kinases was observed on a similar timescale and involved the internalisation and accumulation or receptor heterodimers within endosomes. These data demonstrate the broad applicability of this novel FLIM technique to the spatio-temporal dynamics of protein-protein interaction.
机译:我们在大规模平行,完全可寻址的时间分辨多光束多光子显微镜中展示了衍射受限的多光子成像,能够产生低于50ps时间分辨率的荧光寿命图像。与单光束激光扫描FLIM相比,该成像平台的采集速度显着提高了64倍,而不会影响系统的时间或空间分辨率。我们展示了表达绿色荧光蛋白的活细胞在500 ms时的FLIM采集。通过观察受体配体刺激后表皮生长因子受体(EGFR)和衔接蛋白Grb2之间的时间依赖性FRET,可以说明该技术对活细胞中蛋白质-蛋白质相互作用成像的适用性。此外,在相似的时间尺度上观察到了HER2-HER3受体酪氨酸激酶的配体依赖性缔合,并涉及内体的内在化和积累或受体异二聚体。这些数据证明了这种新颖的FLIM技术在蛋白质-蛋白质相互作用的时空动力学方面具有广泛的适用性。

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