Connexin 46 and connexin 50 gap junction channel properties are shaped by structural and dynamic features of their N-terminal domains.
| Autor: | Yue B; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada., Haddad BG; Department of Chemistry, Portland State University, Portland, OR, 97201, USA., Khan U; Department of Chemistry, Portland State University, Portland, OR, 97201, USA., Chen H; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada., Atalla M; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada., Zhang Z; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada., Zuckerman DM; Department of Biomedical Engineering, Oregon Health and Science University, Portland, OR, 97239, USA., Reichow SL; Department of Chemistry, Portland State University, Portland, OR, 97201, USA., Bai D; Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada. |
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| Jazyk: | angličtina |
| Zdroj: | The Journal of physiology [J Physiol] 2021 Jul; Vol. 599 (13), pp. 3313-3335. Date of Electronic Publication: 2021 May 13. |
| DOI: | 10.1113/JP281339 |
| Abstrakt: | Key Points: Gap junctions formed by different connexins are expressed throughout the body and harbour unique channel properties that have not been fully defined mechanistically. Recent structural studies by cryo-electron microscopy have produced high-resolution models of the related but functionally distinct lens connexins (Cx50 and Cx46) captured in a stable open state, opening the door for structure-function comparison. Here, we conducted comparative molecular dynamics simulation and electrophysiology studies to dissect the isoform-specific differences in Cx46 and Cx50 intercellular channel function. We show that key determinants Cx46 and Cx50 gap junction channel open stability and unitary conductance are shaped by structural and dynamic features of their N-terminal domains, in particular the residue at the 9th position and differences in hydrophobic anchoring sites. The results of this study establish the open state Cx46/50 structural models as archetypes for structure-function studies targeted at elucidating the mechanism of gap junction channels and the molecular basis of disease-causing variants. Abstract: Connexins form intercellular communication channels, known as gap junctions (GJs), that facilitate diverse physiological roles, from long-range electrical and chemical coupling to coordinating development and nutrient exchange. GJs formed by different connexin isoforms harbour unique channel properties that have not been fully defined mechanistically. Recent structural studies on Cx46 and Cx50 defined a novel and stable open state and implicated the amino-terminal (NT) domain as a major contributor for isoform-specific functional differences between these closely related lens connexins. To better understand these differences, we constructed models corresponding to wildtype Cx50 and Cx46 GJs, NT domain swapped chimeras, and point variants at the 9th residue for comparative molecular dynamics (MD) simulation and electrophysiology studies. All constructs formed functional GJ channels, except the chimeric Cx46-50NT variant, which correlated with an introduced steric clash and increased dynamical behaviour (instability) of the NT domain observed by MD simulation. Single channel conductance correlated well with free-energy landscapes predicted by MD, but resulted in a surprisingly greater degree of effect. Additionally, we observed significant effects on transjunctional voltage-dependent gating (V (© 2021 The Authors. The Journal of Physiology © 2021 The Physiological Society.) |
| Databáze: | MEDLINE |
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