Svensson Frida R, Abrahamsson Maria, Strömberg Niklas, Ewing Andrew G, Lincoln Per
Department of Chemical and Biological Engineering, Chalmers University of Technology, Kemivägen 10, SE-41296 Gothenburg, Sweden.
J Phys Chem Lett. 2011 Feb 7;2(5):397-401. doi: 10.1021/jz101580e.
Ruthenium dipyridophenazine (dppz) complexes are sensitive luminescent probes for hydrophobic environments. Here, we apply multiple-frequency fluorescence lifetime imaging microscopy (FLIM) to Δ and Λ enantiomers of lipophilic ruthenium dppz complexes in live and fixed cells, and their different lifetime staining patterns are related to conventional intensity-based microscopy. Excited state lifetimes of the enantiomers determined from FLIM measurements correspond well with spectroscopically measured emission decay curves in pure microenvironments of DNA, phospholipid membrane or a model protein. We show that FLIM can be applied to monitor the long-lived excited states of ruthenium complex enantiomers and, combined with confocal microscopy, give new insight into their biomolecular binding and reveal differences in the microenvironment probed by the complexes.
钌二吡啶菲咯啉(dppz)配合物是用于疏水环境的灵敏发光探针。在此,我们将多频荧光寿命成像显微镜(FLIM)应用于活细胞和固定细胞中亲脂性钌dppz配合物的Δ和Λ对映体,并且它们不同的寿命染色模式与传统的基于强度的显微镜相关。通过FLIM测量确定的对映体激发态寿命与在DNA、磷脂膜或模型蛋白的纯微环境中光谱测量的发射衰减曲线非常吻合。我们表明,FLIM可用于监测钌配合物对映体的长寿命激发态,并且与共聚焦显微镜相结合,能对其生物分子结合提供新的见解,并揭示配合物所探测的微环境中的差异。