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Regulation of a pentameric ligand-gated ion channel by a semiconserved cationic lipid-binding site
- Source :
- The Journal of Biological Chemistry, Journal of Biological Chemistry
- Publication Year :
- 2021
- Publisher :
- American Society for Biochemistry and Molecular Biology, 2021.
-
Abstract
- Pentameric ligand-gated ion channels (pLGICs) are crucial mediators of electrochemical signal transduction in various organisms from bacteria to humans. Lipids play an important role in regulating pLGIC function, yet the structural bases for specific pLGIC-lipid interactions remain poorly understood. The bacterial channel ELIC recapitulates several properties of eukaryotic pLGICs, including activation by the neurotransmitter GABA and binding and modulation by lipids, offering a simplified model system for structure-function relationship studies. In this study, functional effects of noncanonical amino acid substitution of a potential lipid-interacting residue (W206) at the top of the M1-helix, combined with detergent interactions observed in recent X-ray structures, are consistent with this region being the location of a lipid-binding site on the outward face of the ELIC transmembrane domain. Coarse-grained and atomistic molecular dynamics simulations revealed preferential binding of lipids containing a positive charge, particularly involving interactions with residue W206, consistent with cation-π binding. Polar contacts from other regions of the protein, particularly M3 residue Q264, further support lipid binding via headgroup ester linkages. Aromatic residues were identified at analogous sites in a handful of eukaryotic family members, including the human GABAA receptor ε subunit, suggesting conservation of relevant interactions in other evolutionary branches. Further mutagenesis experiments indicated that mutations at this site in ε-containing GABAA receptors can change the apparent affinity of the agonist response to GABA, suggesting a potential role of this site in channel gating. In conclusion, this work details type-specific lipid interactions, which adds to our growing understanding of how lipids modulate pLGICs. ispartof: JOURNAL OF BIOLOGICAL CHEMISTRY vol:297 issue:2 ispartof: location:United States status: published
- Subjects :
- DYNAMICS
MECHANISM
0301 basic medicine
Models, Molecular
POPG, palmitoyloleoylphosphatidylglycerol
TMD, transmembrane domain
DOTAP, dipalmitoyl-3-trimethylammonium-propane
PG, phosphatidylglycerol
Crystallography, X-Ray
Biochemistry
ACTIVATION
chemistry.chemical_compound
PC, phosphatidylcholine
Xenopus laevis
Chemistry
GABAA receptor
Editors' Pick
Lipids
Transmembrane domain
VSD, voltage-sensor domain
K+ CHANNEL
Ligand-gated ion channel
Protein Structural Elements
Signal transduction
site-directed mutagenesis
Life Sciences & Biomedicine
Research Article
Protein Binding
STRUCTURAL BASIS
Biochemistry & Molecular Biology
SOFTWARE NEWS
Protein subunit
ICD, intracellular domain
Cys-loop receptor
POPC, palmitoyloleoylphosphatidylcholine
PE, phosphatidylethanolamine
Cell Line
03 medical and health sciences
pLGIC, pentameric ligand-gated ion channel
Cations
Animals
Humans
Molecular Biology
POPC
Ion channel
G protein-coupled receptor
GPCR, G-protein-coupled receptor
Science & Technology
RECEPTOR
030102 biochemistry & molecular biology
RMSD, root-mean-squared deviation
Cell Biology
Ligand-Gated Ion Channels
electrophysiology
nAChR, nicotinic acetylcholine receptor
ECD, extracellular domain
WT, wild-type
molecular dynamics
PROTEIN INTERACTIONS
030104 developmental biology
GENERAL-ANESTHETICS
Biophysics
Oocytes
ELIC
pentameric ligand-gated ion channel
X-RAY-STRUCTURE
Subjects
Details
- Language :
- English
- ISSN :
- 1083351X and 00219258
- Volume :
- 297
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- The Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....a1b160ea3186d551ffde4ccf17635eb8