PT  - JOURNAL ARTICLE
AU  - Agenor Limon
AU  - Argel Estrada-Mondragon
AU  - Jorge M Reyes-Ruiz
AU  - Ricardo Miledi
TI  - Dipicrylamine Modulates GABAρ1 Receptors through Interactions with Residues in the TM4 and Cys-loop Domains
AID  - 10.1124/mol.116.103432
DP  - 2016 Jan 01
TA  - Molecular Pharmacology
PG  - mol.116.103432
4099  - http://molpharm.aspetjournals.org/content/early/2016/02/11/mol.116.103432.short
4100  - http://molpharm.aspetjournals.org/content/early/2016/02/11/mol.116.103432.full
AB  - Dipicrylamine (DPA) is a commonly used acceptor agent in Forster resonance energy transfer (FRET) experiments that allows the study of high frequency neuronal activity in the optical-monitoring of voltage in living cells. However, DPA potently antagonizes GABAA receptors (GABAARs) that contain α1 and β2 subunits by a mechanism which is not clearly understood. In this work, we aimed to determine whether DPA modulation is a general phenomenon of Cys-loop ligand-gated ion channels (LGICs) and whether this modulation depends on particular amino acid residues. For this we studied the effects of DPA on human homomeric GABAρ1, α7 nicotinic and 5-HT3A receptors expressed in Xenopus oocytes. Our results indicate that DPA is an allosteric modulator of GABAρ1 receptors with an IC50 of 1.6 μM, an enhancer of α7 nicotinic receptors at relatively high concentrations of DPA, and has little, if any, effect on 5-HT3A receptors. DPA antagonism of GABAρ1 was strongly enhanced by pre-incubation, was slightly voltage-dependent, and its washout was accelerated by bovine serum albumin. These results indicate that DPA modulation is not a general phenomenon of LGICs and structural differences between receptors may account for disparities in DPA effects. In silico modeling of DPA docking to GABAρ1, α7 nicotinic and 5-HT3A receptors suggests that a hydrophobic pocket within the Cys-loop and the M4 segment in GABAρ1, located at the extracellular/membrane interface, facilitates the interaction with DPA that leads to inhibition of the receptor. Functional examinations of mutant receptors support the involvement of the M4 segment in the allosteric modulation of GABAρ1 by DPA.