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An E3-ligase-based method for ablating inhibitory synapses.
Gross, Garrett G; Straub, Christoph; Perez-Sanchez, Jimena; Dempsey, William P; Junge, Jason A; Roberts, Richard W; Trinh, Le A; Fraser, Scott E; De Koninck, Yves; De Koninck, Paul; Sabatini, Bernardo L; Arnold, Don B.
Afiliação
  • Gross GG; Department of Biology, Section of Molecular and Computational Biology, University of Southern California, Los Angeles, Los Angeles, California, USA.
  • Straub C; Howard Hughes Medical Institute, Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.
  • Perez-Sanchez J; Centre de recherche, Institut universitaire en santé mentale de Québec, Québec, Québec, Canada.
  • Dempsey WP; Université Laval, Québec, Québec, Canada.
  • Junge JA; Department of Biology, Section of Molecular and Computational Biology, University of Southern California, Los Angeles, Los Angeles, California, USA.
  • Roberts RW; Department of Biology, Section of Molecular and Computational Biology, University of Southern California, Los Angeles, Los Angeles, California, USA.
  • Trinh le A; Department of Chemistry, University of Southern California, Los Angeles, Los Angeles, California, USA.
  • Fraser SE; Department of Biology, Section of Molecular and Computational Biology, University of Southern California, Los Angeles, Los Angeles, California, USA.
  • De Koninck Y; Department of Biology, Section of Molecular and Computational Biology, University of Southern California, Los Angeles, Los Angeles, California, USA.
  • De Koninck P; Centre de recherche, Institut universitaire en santé mentale de Québec, Québec, Québec, Canada.
  • Sabatini BL; Université Laval, Québec, Québec, Canada.
  • Arnold DB; Centre de recherche, Institut universitaire en santé mentale de Québec, Québec, Québec, Canada.
Nat Methods ; 13(8): 673-8, 2016 08.
Article em En | MEDLINE | ID: mdl-27271196
ABSTRACT
Although neuronal activity can be modulated using a variety of techniques, there are currently few methods for controlling neuronal connectivity. We introduce a tool (GFE3) that mediates the fast, specific and reversible elimination of inhibitory synaptic inputs onto genetically determined neurons. GFE3 is a fusion between an E3 ligase, which mediates the ubiquitination and rapid degradation of proteins, and a recombinant, antibody-like protein (FingR) that binds to gephyrin. Expression of GFE3 leads to a strong and specific reduction of gephyrin in culture or in vivo and to a substantial decrease in phasic inhibition onto cells that express GFE3. By temporarily expressing GFE3 we showed that inhibitory synapses regrow following ablation. Thus, we have created a simple, reversible method for modulating inhibitory synaptic input onto genetically determined cells.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinapses / Proteínas de Transporte / Transmissão Sináptica / Técnicas de Patch-Clamp / Ubiquitina-Proteína Ligases / Proteínas de Membrana / Neurônios Limite: Animals Idioma: En Revista: Nat Methods Assunto da revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinapses / Proteínas de Transporte / Transmissão Sináptica / Técnicas de Patch-Clamp / Ubiquitina-Proteína Ligases / Proteínas de Membrana / Neurônios Limite: Animals Idioma: En Revista: Nat Methods Assunto da revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos