Lesiak Lauren, Dadina Neville, Zheng Shuai, Schelvis Marianne, Schepartz Alanna
Department of Chemistry, University of California, Berkeley, California 94720, United States.
bioRxiv. 2023 Aug 4:2023.08.04.552058. doi: 10.1101/2023.08.04.552058.
Lysosomes have long been known for their acidic lumen and efficient degradation of cellular byproducts. In recent years it has become clear that their function is far more sophisticated, involving multiple cell signaling pathways and interactions with other organelles. Unfortunately, their acidic interior, fast dynamics, and small size makes lysosomes difficult to image with fluorescence microscopy. Here we report a far-red small molecule, HMSiR-Me, that fluoresces only under acidic conditions, causing selective labeling of acidic organelles in live cells. HMSiR-Me can be used alongside other far-red dyes in multicolor imaging experiments and is superior to existing lysosome probes in terms of photostability and maintaining cell health and lysosome motility. We demonstrate that HMSiR-Me is compatible with overnight time lapse experiments, as well as time lapse super-resolution microscopy with a fast frame rate for at least 1000 frames. HMSiR-Me can also be used alongside silicon rhodamine dyes in a multiplexed super-resolution microscopy experiment to visualize interactions between the inner mitochondrial membrane and lysosomes with only a single excitation laser and simultaneous depletion. We envision this dye permitting more detailed study of the role of lysosomes in dynamic cellular processes and disease.
长期以来,溶酶体因其酸性内腔和对细胞副产物的高效降解而闻名。近年来,人们越来越清楚地认识到,溶酶体的功能要复杂得多,涉及多种细胞信号通路以及与其他细胞器的相互作用。不幸的是,溶酶体的酸性内部环境、快速的动态变化以及较小的尺寸使得用荧光显微镜对其进行成像变得困难。在此,我们报告一种远红色小分子HMSiR-Me,它仅在酸性条件下发出荧光,从而实现对活细胞中酸性细胞器的选择性标记。HMSiR-Me可在多色成像实验中与其他远红色染料一起使用,并且在光稳定性以及维持细胞健康和溶酶体运动性方面优于现有的溶酶体探针。我们证明,HMSiR-Me适用于过夜延时实验,以及至少1000帧的快速帧率的延时超分辨率显微镜实验。HMSiR-Me还可在多重超分辨率显微镜实验中与硅罗丹明染料一起使用,仅用单一激发激光和同时耗尽来可视化线粒体内膜与溶酶体之间的相互作用。我们设想这种染料将有助于更详细地研究溶酶体在动态细胞过程和疾病中的作用。