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A super-resolution platform for correlative live single-molecule imaging and STED microscopy.
Inavalli, V V G Krishna; Lenz, Martin O; Butler, Corey; Angibaud, Julie; Compans, Benjamin; Levet, Florian; Tønnesen, Jan; Rossier, Olivier; Giannone, Gregory; Thoumine, Olivier; Hosy, Eric; Choquet, Daniel; Sibarita, Jean-Baptiste; Nägerl, U Valentin.
Afiliação
  • Inavalli VVGK; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
  • Lenz MO; Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
  • Butler C; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
  • Angibaud J; Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
  • Compans B; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
  • Levet F; Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
  • Tønnesen J; Imagine Optic, Orsay, France.
  • Rossier O; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
  • Giannone G; Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
  • Thoumine O; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
  • Hosy E; Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
  • Choquet D; Interdisciplinary Institute for Neuroscience, University of Bordeaux, Bordeaux, France.
  • Sibarita JB; Interdisciplinary Institute for Neuroscience, CNRS UMR 5297, Bordeaux, France.
  • Nägerl UV; Bordeaux Imaging Center, CNRS UMS 3420, University of Bordeaux, INSERM US04, Bordeaux, France.
Nat Methods ; 16(12): 1263-1268, 2019 12.
Article em En | MEDLINE | ID: mdl-31636458
ABSTRACT
Super-resolution microscopy offers tremendous opportunities to unravel the complex and dynamic architecture of living cells. However, current super-resolution microscopes are well suited for revealing protein distributions or cell morphology, but not both. We present a super-resolution platform that permits correlative single-molecule imaging and stimulated emission depletion microscopy in live cells. It gives nanoscale access to the positions and movements of synaptic proteins within the morphological context of growth cones and dendritic spines.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Imagem Individual de Molécula / Microscopia de Fluorescência Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Imagem Individual de Molécula / Microscopia de Fluorescência Limite: Animals / Female / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article