A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Membrane-Dependent Binding and Entry Mechanism of Dopamine into Its Receptor
Tekijät: Lolicato F, Juhola H, Zak A, Postila PA, Saukko A, Rissanen S, Enkavi G, Vattulainen I, Kepczynski M, Rog T
Kustantaja: AMER CHEMICAL SOC
Julkaisuvuosi: 2020
Journal: ACS Chemical Neuroscience
Tietokannassa oleva lehden nimi: ACS CHEMICAL NEUROSCIENCE
Lehden akronyymi: ACS CHEM NEUROSCI
Vuosikerta: 11
Numero: 13
Aloitussivu: 1914
Lopetussivu: 1924
Sivujen määrä: 11
ISSN: 1948-7193
DOI: https://doi.org/10.1021/acschemneuro.9b00656
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/49280021
Synaptic neurotransmission has recently been proposed to function via either a membrane-independent or a membrane-dependent mechanism, depending on the neurotransmitter type. In the membrane-dependent mechanism, amphipathic neurotransmitters first partition to the lipid headgroup region and then diffuse along the membrane plane to their membrane-buried receptors. However, to date, this mechanism has not been demonstrated for any neurotransmitter-receptor complex. Here, we combined isothermal calorimetry measurements with a diverse set of molecular dynamics simulation methods to investigate the partitioning of an amphipathic neurotransmitter (dopamine) and the mechanism of its entry into the ligand-binding site. Our results show that the binding of dopamine to its receptor is consistent with the membrane-dependent binding and entry mechanism. Both experimental and simulation results showed that dopamine favors binding to lipid membranes especially in the headgroup region. Moreover, our simulations revealed a ligand-entry pathway from the membrane to the binding site. This pathway passes through a lateral gate between transmembrane alpha-helices 5 and 6 on the membrane-facing side of the protein. All in all, our results demonstrate that dopamine binds to its receptor by a membrane-dependent mechanism, and this is complemented by the more traditional binding mechanism directly through the aqueous phase. The results suggest that the membrane-dependent mechanism is common in other synaptic receptors, too.
Ladattava julkaisu This is an electronic reprint of the original article. |  |
