| Literature DB >> 34312564 |
L Silvestri1,2,3, M C Müllenbroich4,5,6, I Costantini4,5,7, A P Di Giovanna4, G Mazzamuto4,5, A Franceschini4, D Kutra8, A Kreshuk8, C Checcucci4,9, L O Toresano9, P Frasconi9, L Sacconi4,5, F S Pavone10,4,5.
Abstract
Unbiased quantitative analysis of macroscopic biological samples demands fast imaging systems capable of maintaining high resolution across large volumes. Here we introduce RAPID (rapid autofocusing via pupil-split image phase detection), a real-time autofocus method applicable in every widefield-based microscope. RAPID-enabled light-sheet microscopy reliably reconstructs intact, cleared mouse brains with subcellular resolution, and allowed us to characterize the three-dimensional (3D) spatial clustering of somatostatin-positive neurons in the whole encephalon, including densely labeled areas. Furthermore, it enabled 3D morphological analysis of microglia across the entire brain. Beyond light-sheet microscopy, we demonstrate that RAPID maintains high image quality in various settings, from in vivo fluorescence imaging to 3D tracking of fast-moving organisms. RAPID thus provides a flexible autofocus solution that is suitable for traditional automated microscopy tasks as well as for quantitative analysis of large biological specimens.Entities:
Year: 2021 PMID: 34312564 DOI: 10.1038/s41592-021-01208-1
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547