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An E3-ligase-based method for ablating inhibitory synapses.

Nature methods (2016-06-09)
Garrett G Gross, Christoph Straub, Jimena Perez-Sanchez, William P Dempsey, Jason A Junge, Richard W Roberts, Le A Trinh, Scott E Fraser, Yves De Koninck, Paul De Koninck, Bernardo L Sabatini, Don B Arnold
RESUMEN

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.

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Monoclonal Anti-β-Tubulin antibody produced in mouse, clone TUB 2.1, ascites fluid
Sigma-Aldrich
Anticuerpo anti-receptor α1 del GABAA, Upstate®, from rabbit