Details

Autor(en) / Beteiligte

• Chen, Bi-Chang
• Legant, Wesley R.
• Wang, Kai
• Shao, Lin
• Milkie, Daniel E.
• Davidson, Michael W.
• Janetopoulos, Chris
• Wu, Xufeng S.
• Hammer, John A.
• Liu, Zhe
• English, Brian P.
• Mimori-Kiyosue, Yuko
• Romero, Daniel P.
• Ritter, Alex T.
• Lippincott-Schwartz, Jennifer
• Fritz-Laylin, Lillian
• Mullins, R. Dyche
• Mitchell, Diana M.
• Bembenek, Joshua N.
• Reymann, Anne-Cecile
• Böhme, Ralph
• Grill, Stephan W.
• Wang, Jennifer T.
• Seydoux, Geraldine
• Tulu, U. Serdar
• Kiehart, Daniel P.
• Betzig, Eric

Titel

Lattice light-sheet microscopy: Imaging molecules to embryos at high spatiotemporal resolution

Ist Teil von

• Science (American Association for the Advancement of Science), 2014-10, Vol.346 (6208), p.439-439

Ort / Verlag

United States: American Association for the Advancement of Science

Erscheinungsjahr

2014

Link zum Volltext

Quelle

American Association for the Advancement of Science

Beschreibungen/Notizen

• Although fluorescence microscopy provides a crucial window into the physiology of living specimens, many biological processes are too fragile, are too small, or occur too rapidly to see clearly with existing tools. We crafted ultrathin light sheets from two-dimensional optical lattices that allowed us to image three-dimensional (3D) dynamics for hundreds of volumes, often at subsecond intervals, at the diffraction limit and beyond. We applied this to systems spanning four orders of magnitude in space and time, including the diffusion of single transcription factor molecules in stem cell spheroids, the dynamic instability of mitotic microtubules, the immunological synapse, neutrophil motility in a 3D matrix, and embryogenesis in Caenorhabditis elegans and Drosophila melanogaster. The results provide a visceral reminder of the beauty and the complexity of living systems.