4.8 Article

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

Journal

NATURE CHEMICAL BIOLOGY
Volume 16, Issue 4, Pages 408-+

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41589-020-0479-z

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Funding

  1. NIH [5T32GM06754 3-12, R01GM131372-01, R01GM118486, S10 OD020142]
  2. Wellcome Trust [095927/A/11/Z]
  3. Wellcome Trust [095927/A/11/Z] Funding Source: Wellcome Trust

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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 DiIC(16)TCO or DiIC(16')TCO followed by in situ tetrazine ligation reaction with the silicon-rhodamine dye SiR-Tz generates the HIDE probes DiIC(16)-SiR and DiIC(16')-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(16)-SiR and DiIC(16')-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.

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