Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 34504004.
- Also identified by DOI 10.1073/pnas.2108006118 and PMC identifier 8449418.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Pentameric ligand-gated ion channels undergo subtle conformational cycling to control electrochemical signal transduction in many kingdoms of life. Several crystal structures have now been reported in this family, but the functional relevance of such models remains unclear. Here, we used small-angle neutron scattering (SANS) to probe ambient solution-phase properties of the pH-gated bacterial ion channel GLIC under resting and activating conditions. Data collection was optimized by inline paused-flow size-exclusion chromatography, and exchanging into deuterated detergent to hide the micelle contribution. Resting-state GLIC was the best-fit crystal structure to SANS curves, with no evidence for divergent mechanisms. Moreover, enhanced-sampling molecular-dynamics simulations enabled differential modeling in resting versus activating conditions, with the latter corresponding to an intermediate ensemble of both the extracellular and transmembrane domains. This work demonstrates state-dependent changes in a pentameric ion channel by SANS, an increasingly accessible method for macromolecular characterization with the coming generation of neutron sources.
Medical subject headings
- Bacterial Proteins
- Ion Channel Gating
- Ligand-Gated Ion Channels
- Neutrons
- Protein Multimerization
- Protein Structure, Quaternary
- Scattering, Small Angle