Abstract
Visual rhodopsin is an important archetype for G-protein-coupled receptors, which are membrane proteins implicated in cellular signal transduction. Herein, we show experimentally that approximately 80 water molecules flood rhodopsin upon light absorption to form a solvent-swollen active state. An influx of mobile water is necessary for activating the photoreceptor, and this finding is supported by molecular dynamics (MD) simulations. Combined force-based measurements involving osmotic and hydrostatic pressure indicate the expansion occurs by changes in cavity volumes, together with greater hydration in the active metarhodopsin-II state. Moreover, we discovered that binding and release of the C-terminal helix of transducin is coupled to hydration changes as may occur in visual signal amplification. Hydration–dehydration explains signaling by a dynamic allosteric mechanism, in which the soft membrane matter (lipids and water) has a pivotal role in the catalytic G-protein cycle.
Original language | English (US) |
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Pages (from-to) | 2288-2295 |
Number of pages | 8 |
Journal | Angewandte Chemie - International Edition |
Volume | 60 |
Issue number | 5 |
DOIs | |
State | Published - Feb 1 2021 |
Keywords
- GPCRs
- membrane lipids
- membrane proteins
- osmotic stress
- rhodopsin
ASJC Scopus subject areas
- Catalysis
- General Chemistry