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A general strategy for developing cell-permeable photo-modulatable organic fluorescent probes for live-cell super-resolution imaging

机译:开发用于活细胞超分辨率成像的可渗透细胞的光调制有机荧光探针的一般策略

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Single-molecule localization microscopy (SMLM) achieves super-resolution imaging beyond the diffraction limit but critically relies on the use of photo-modulatable fluorescent probes. Here we report a general strategy for constructing cell-permeable photo-modulatable organic fluorescent probes for live-cell SMLM by exploiting the remarkable cytosolic delivery ability of a cell-penetrating peptide (rR)(3)R-2. We develop photo-modulatable organic fluorescent probes consisting of a (rR)(3)R-2 peptide coupled to a cell-impermeable organic fluorophore and a recognition unit. Our results indicate that these organic probes are not only cell permeable but can also specifically and directly label endogenous targeted proteins. Using the probes, we obtain super-resolution images of lysosomes and endogenous F-actin under physiological conditions. We resolve the dynamics of F-actin with 10 s temporal resolution in live cells and discern fine F-actin structures with diameters of similar to 80 nm. These results open up new avenues in the design of fluorescent probes for live-cell super-resolution imaging.
机译:单分子定位显微镜(SMLM)可以实现超出衍射极限的超分辨率成像,但关键是要依靠光调制荧光探针的使用。在这里,我们报告通过利用细胞穿透肽(rR)(3)R-2的显着细胞溶质传递能力,为活细胞SMLM构建细胞可渗透的可光调制有机荧光探针的一般策略。我们开发的光调制有机荧光探针由(rR)(3)R-2肽偶联到细胞不可渗透的有机荧光团和识别单元组成。我们的结果表明,这些有机探针不仅可以穿透细胞,而且可以特异性地直接标记内源性靶向蛋白质。使用探针,我们获得了在生理条件下溶酶体和内源性F-肌动蛋白的超分辨率图像。我们以10 s的时间分辨率解决了活细胞中F-肌动蛋白的动力学问题,并发现了直径类似于80 nm的精细F-肌动蛋白结构。这些结果为活细胞超分辨率成像的荧光探针设计开辟了新途径。

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