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Genetic Code Expansion and Click-Chemistry Labeling to Visualize GABA-A Receptors by Super-Resolution Microscopy.
Kuhlemann, Alexander; Beliu, Gerti; Janzen, Dieter; Petrini, Enrica Maria; Taban, Danush; Helmerich, Dominic A; Doose, Sören; Bruno, Martina; Barberis, Andrea; Villmann, Carmen; Sauer, Markus; Werner, Christian.
Afiliación
  • Kuhlemann A; Department of Biotechnology and Biophysics, University of Würzburg, Biocenter, Würzburg, Germany.
  • Beliu G; Department of Biotechnology and Biophysics, University of Würzburg, Biocenter, Würzburg, Germany.
  • Janzen D; Rudolf Virchow Center for Integrative and Translational Bioimaging, University of Wuerzburg, Würzburg, Germany.
  • Petrini EM; Institute of Clinical Neurobiology, University of Würzburg, Würzburg, Germany.
  • Taban D; Neuroscience and Brain Technologies Department, Istituto Italiano Di Tecnologia, Genova, Italy.
  • Helmerich DA; Department of Biotechnology and Biophysics, University of Würzburg, Biocenter, Würzburg, Germany.
  • Doose S; Department of Biotechnology and Biophysics, University of Würzburg, Biocenter, Würzburg, Germany.
  • Bruno M; Department of Biotechnology and Biophysics, University of Würzburg, Biocenter, Würzburg, Germany.
  • Barberis A; Neuroscience and Brain Technologies Department, Istituto Italiano Di Tecnologia, Genova, Italy.
  • Villmann C; Neuroscience and Brain Technologies Department, Istituto Italiano Di Tecnologia, Genova, Italy.
  • Sauer M; Institute of Clinical Neurobiology, University of Würzburg, Würzburg, Germany.
  • Werner C; Department of Biotechnology and Biophysics, University of Würzburg, Biocenter, Würzburg, Germany.
Front Synaptic Neurosci ; 13: 727406, 2021.
Article en En | MEDLINE | ID: mdl-34899260
ABSTRACT
Fluorescence labeling of difficult to access protein sites, e.g., in confined compartments, requires small fluorescent labels that can be covalently tethered at well-defined positions with high efficiency. Here, we report site-specific labeling of the extracellular domain of γ-aminobutyric acid type A (GABA-A) receptor subunits by genetic code expansion (GCE) with unnatural amino acids (ncAA) combined with bioorthogonal click-chemistry labeling with tetrazine dyes in HEK-293-T cells and primary cultured neurons. After optimization of GABA-A receptor expression and labeling efficiency, most effective variants were selected for super-resolution microscopy and functionality testing by whole-cell patch clamp. Our results show that GCE with ncAA and bioorthogonal click labeling with small tetrazine dyes represents a versatile method for highly efficient site-specific fluorescence labeling of proteins in a crowded environment, e.g., extracellular protein domains in confined compartments such as the synaptic cleft.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Synaptic Neurosci Año: 2021 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Front Synaptic Neurosci Año: 2021 Tipo del documento: Article País de afiliación: Alemania