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利用 HIDE 探针在活细胞中超分辨率观察到内体运动缺陷。

Endosome motility defects revealed at super-resolution in live cells using HIDE probes.

机构信息

Department of Chemistry, Yale University, New Haven, CT, USA.

Department of Cell Biology, Yale University School of Medicine, New Haven, CT, USA.

出版信息

Nat Chem Biol. 2020 Apr;16(4):408-414. doi: 10.1038/s41589-020-0479-z. Epub 2020 Feb 24.

Abstract

We report new lipid-based, high-density, environmentally sensitive (HIDE) probes that accurately and selectively image endo-lysosomes and their dynamics at super-resolution for extended times. Treatment of live cells with the small molecules DiICTCO or DiICTCO followed by in situ tetrazine ligation reaction with the silicon-rhodamine dye SiR-Tz generates the HIDE probes DiIC-SiR and DiIC-SiR in the endo-lysosomal membrane. These new probes support the acquisition of super-resolution videos of organelle dynamics in primary cells for more than 7 min with no detectable change in endosome structure or function. Using DiIC-SiR and DiIC-SiR, we describe direct evidence of endosome motility defects in cells from patients with Niemann-Pick Type-C disease. In wild-type fibroblasts, the probes reveal distinct but rare inter-endosome kiss-and-run events that cannot be observed using confocal methods. Our results shed new light on the role of NPC1 in organelle motility and cholesterol trafficking.

摘要

我们报告了新的基于脂质的高密度、环境敏感(HIDE)探针,这些探针可以在超分辨率下准确且选择性地成像内体溶酶体及其动力学,并能长时间扩展观察。用小分子 DiICTCO 处理活细胞,然后用硅罗丹明染料 SiR-Tz 进行原位四嗪连接反应,在内涵体膜中生成 HIDE 探针 DiIC-SiR 和 DiIC-SiR。这些新探针支持在原代细胞中获取细胞器动力学的超分辨率视频,超过 7 分钟,而内体结构或功能没有可检测到的变化。使用 DiIC-SiR 和 DiIC-SiR,我们描述了 NPC1 缺陷型细胞中内体运动缺陷的直接证据。在野生型成纤维细胞中,探针揭示了独特但罕见的内体融合-破裂事件,使用共聚焦方法无法观察到这些事件。我们的结果为 NPC1 在细胞器运动和胆固醇运输中的作用提供了新的线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53c9/7176048/4cd0ca42efc1/nihms-1549978-f0001.jpg

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