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Volumetric imaging of fast cellular dynamics with deep learning enhanced bioluminescence microscopy.
Morales-Curiel, Luis Felipe; Gonzalez, Adriana Carolina; Castro-Olvera, Gustavo; Lin, Li-Chun Lynn; El-Quessny, Malak; Porta-de-la-Riva, Montserrat; Severino, Jacqueline; Morera, Laura Battle; Venturini, Valeria; Ruprecht, Verena; Ramallo, Diego; Loza-Alvarez, Pablo; Krieg, Michael.
Afiliação
  • Morales-Curiel LF; ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
  • Gonzalez AC; ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
  • Castro-Olvera G; ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
  • Lin LL; ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
  • El-Quessny M; ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
  • Porta-de-la-Riva M; ICFO, Institut de Ciencies Fotòniques, Castelldefels, Spain.
  • Severino J; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Morera LB; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Venturini V; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Ruprecht V; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Ramallo D; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
  • Loza-Alvarez P; Universitat Pompeu Fabra (UPF), Barcelona, Spain.
  • Krieg M; ICREA, Pg. Lluis Companys 23, 08010, Barcelona, Spain.
Commun Biol ; 5(1): 1330, 2022 12 03.
Article em En | MEDLINE | ID: mdl-36463346
Bioluminescence microscopy is an appealing alternative to fluorescence microscopy, because it does not depend on external illumination, and consequently does neither produce spurious background autofluorescence, nor perturb intrinsically photosensitive processes in living cells and animals. The low photon emission of known luciferases, however, demands long exposure times that are prohibitive for imaging fast biological dynamics. To increase the versatility of bioluminescence microscopy, we present an improved low-light microscope in combination with deep learning methods to image extremely photon-starved samples enabling subsecond exposures for timelapse and volumetric imaging. We apply our method to image subcellular dynamics in mouse embryonic stem cells, epithelial morphology during zebrafish development, and DAF-16 FoxO transcription factor shuttling from the cytoplasm to the nucleus under external stress. Finally, we concatenate neural networks for denoising and light-field deconvolution to resolve intracellular calcium dynamics in three dimensions of freely moving Caenorhabditis elegans.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aprendizado Profundo Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Aprendizado Profundo Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article