Modulation of the erwinia ligand-gated ion channel (ELIC) and the 5-HT3 receptor via a common vestibule site

Marijke Brams, Cedric Govaerts, Kumiko Kambara, Kerry Price, Radovan Spurny, Anant Gharpure, Els Pardon, Genevieve L. Evans, Daniel Bertrand, Sarah C.R. Lummis, Ryan E. Hibbs, Jan Steyaert, Chris Ulens

Research output: Contribution to journalArticlepeer-review

4 Scopus citations


Pentameric ligand-gated ion channels (pLGICs) or Cys-loop receptors are involved in fast synaptic signaling in the nervous system. Allosteric modulators bind to sites that are remote from the neurotransmitter binding site, but modify coupling of ligand binding to channel opening. In this study, we developed nanobodies (single domain antibodies), which are functionally active as allosteric modulators, and solved co-crystal structures of the prokaryote (Erwinia) channel ELIC bound either to a positive or a negative allosteric modulator. The allosteric nanobody binding sites partially overlap with those of small molecule modulators, including a vestibule binding site that is not accessible in some pLGICs. Using mutagenesis, we extrapolate the functional importance of the vestibule binding site to the human 5-HT3 receptor, suggesting a common mechanism of modulation in this protein and ELIC. Thus we identify key elements of allosteric binding sites, and extend drug design possibilities in pLGICs with an accessible vestibule site.

Original languageEnglish (US)
Article numbere51511
StatePublished - Jan 2020

ASJC Scopus subject areas

  • Neuroscience(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)


Dive into the research topics of 'Modulation of the erwinia ligand-gated ion channel (ELIC) and the 5-HT3 receptor via a common vestibule site'. Together they form a unique fingerprint.

Cite this