Universal autofocus for quantitative volumetric microscopy of whole mouse brains.
Ludovico SilvestriMarie Caroline MüllenbroichIrene CostantiniA P Di GiovannaGiacomo MazzamutoA FranceschiniDominik KutraAnna KreshukCurzio CheccucciL O ToresanoP FrasconiLeonardo SacconiF S PavonePublished in: Nature methods (2021)
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.
Keyphrases
- high resolution
- loop mediated isothermal amplification
- single molecule
- fluorescence imaging
- high speed
- high throughput
- mass spectrometry
- label free
- machine learning
- photodynamic therapy
- tandem mass spectrometry
- multiple sclerosis
- working memory
- magnetic resonance imaging
- gram negative
- magnetic resonance
- single cell
- white matter
- inflammatory response
- resting state
- real time pcr
- quantum dots