III. Institute of Physics - Biophysics, Georg August University, 37077, Göttingen, Germany.
Department of Child and Adolescent Health, University Medical Center Göttingen, 37073, Göttingen, Germany.
Commun Biol. 2022 Jan 11;5(1):38. doi: 10.1038/s42003-021-02976-4.
DNA point accumulation for imaging in nanoscale topography (DNA-PAINT) is a powerful super-resolution technique highly suitable for multi-target (multiplexing) bio-imaging. However, multiplexed imaging of cells is still challenging due to the dense and sticky environment inside a cell. Here, we combine fluorescence lifetime imaging microscopy (FLIM) with DNA-PAINT and use the lifetime information as a multiplexing parameter for targets identification. In contrast to Exchange-PAINT, fluorescence lifetime PAINT (FL-PAINT) can image multiple targets simultaneously and does not require any fluid exchange, thus leaving the sample undisturbed and making the use of flow chambers/microfluidic systems unnecessary. We demonstrate the potential of FL-PAINT by simultaneous imaging of up to three targets in a cell using both wide-field FLIM and 3D time-resolved confocal laser scanning microscopy (CLSM). FL-PAINT can be readily combined with other existing techniques of multiplexed imaging and is therefore a perfect candidate for high-throughput multi-target bio-imaging.
DNA 点积累成像纳米形貌(DNA-PAINT)是一种强大的超分辨率技术,非常适合多靶点(多重)生物成像。然而,由于细胞内部密集而粘稠的环境,对细胞进行多重成像仍然具有挑战性。在这里,我们将荧光寿命成像显微镜(FLIM)与 DNA-PAINT 相结合,并将寿命信息用作目标识别的多重化参数。与交换 PAINT(Exchange-PAINT)不同,荧光寿命 PAINT(FL-PAINT)可以同时对多个目标成像,并且不需要任何流体交换,从而使样品不受干扰,无需使用流动池/微流控系统。我们通过使用宽场 FLIM 和 3D 时间分辨共焦激光扫描显微镜(CLSM)在细胞中同时对多达三个目标进行成像,证明了 FL-PAINT 的潜力。FL-PAINT 可以很容易地与其他现有的多重成像技术相结合,因此是高通量多靶点生物成像的理想选择。