Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
Proc Natl Acad Sci U S A. 2012 Aug 28;109(35):13978-83. doi: 10.1073/pnas.1201882109. Epub 2012 Aug 13.
Imaging membranes in live cells with nanometer-scale resolution promises to reveal ultrastructural dynamics of organelles that are essential for cellular functions. In this work, we identified photoswitchable membrane probes and obtained super-resolution fluorescence images of cellular membranes. We demonstrated the photoswitching capabilities of eight commonly used membrane probes, each specific to the plasma membrane, mitochondria, the endoplasmic recticulum (ER) or lysosomes. These small-molecule probes readily label live cells with high probe densities. Using these probes, we achieved dynamic imaging of specific membrane structures in living cells with 30-60 nm spatial resolution at temporal resolutions down to 1-2 s. Moreover, by using spectrally distinguishable probes, we obtained two-color super-resolution images of mitochondria and the ER. We observed previously obscured details of morphological dynamics of mitochondrial fusion/fission and ER remodeling, as well as heterogeneous membrane diffusivity on neuronal processes.
用纳米级分辨率对活细胞中的膜成像有望揭示细胞器的超微结构动态,这些动态对于细胞功能至关重要。在这项工作中,我们鉴定了可光激活的膜探针,并获得了细胞膜的超分辨率荧光图像。我们展示了 8 种常用膜探针的光激活能力,每种探针都特异性标记质膜、线粒体、内质网(ER)或溶酶体。这些小分子探针很容易以高探针密度标记活细胞。利用这些探针,我们实现了活细胞中特定膜结构的动态成像,空间分辨率达到 30-60nm,时间分辨率低至 1-2s。此外,通过使用可区分光谱的探针,我们获得了线粒体和 ER 的双色超分辨率图像。我们观察到线粒体融合/裂变和 ER 重塑的形态动力学以及神经元突起上的膜异质性扩散之前被掩盖的细节。