| Literature DB >> 25342811 |
Bi-Chang Chen1, Wesley R Legant1, Kai Wang1, Lin Shao1, Daniel E Milkie2, Michael W Davidson3, Chris Janetopoulos4, Xufeng S Wu5, John A Hammer5, Zhe Liu1, Brian P English1, Yuko Mimori-Kiyosue6, Daniel P Romero7, Alex T Ritter8, Jennifer Lippincott-Schwartz9, Lillian Fritz-Laylin10, R Dyche Mullins10, Diana M Mitchell11, Joshua N Bembenek11, Anne-Cecile Reymann12, Ralph Böhme12, Stephan W Grill12, Jennifer T Wang13, Geraldine Seydoux13, U Serdar Tulu14, Daniel P Kiehart14, Eric Betzig15.
Abstract
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.Entities:
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Year: 2014 PMID: 25342811 PMCID: PMC4336192 DOI: 10.1126/science.1257998
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728