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Cumulative hydropathic topology of a voltage-gated sodium channel at atomic resolution.
Xenakis, Markos N; Kapetis, Dimos; Yang, Yang; Heijman, Jordi; Waxman, Stephen G; Lauria, Giuseppe; Faber, Catharina G; Smeets, Hubert J; Westra, Ronald L; Lindsey, Patrick J.
Affiliation
  • Xenakis MN; Department of Genetics and Cell Biology, Section Clinical Genomics, Maastricht University, Maastricht, the Netherlands.
  • Kapetis D; School for Mental Health and Neuroscience (MHeNS), Maastricht University, Maastricht, the Netherlands.
  • Yang Y; Neuroalgology Unit, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Heijman J; Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University College of Pharmacy, West Lafayette, Indiana, USA.
  • Waxman SG; Purdue Institute for Integrative Neuroscience, West Lafayette, Indiana, USA.
  • Lauria G; Department of Cardiology, CARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, the Netherlands.
  • Faber CG; Department of Neurology and Center for Neuroscience and Regeneration Research, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Smeets HJ; Rehabilitation Research Center, Veterans Affairs Connecticut Healthcare System, West Haven, Connecticut, USA.
  • Westra RL; Neuroalgology Unit, Fondazione IRCCS Istituto Neurologico "Carlo Besta", Milan, Italy.
  • Lindsey PJ; Department of Biomedical and Clinical Sciences "Luigi Sacco", University of Milan, Milan, Italy.
Proteins ; 88(10): 1319-1328, 2020 10.
Article in En | MEDLINE | ID: mdl-32447794
Voltage-gated sodium channels (NavChs) are biological pores that control the flow of sodium ions through the cell membrane. In humans, mutations in genes encoding NavChs can disrupt physiological cellular activity thus leading to a wide spectrum of diseases. Here, we present a topological connection between the functional architecture of a NavAb bacterial channel and accumulation of atomic hydropathicity around its pore. This connection is established via a scaling analysis methodology that elucidates how intrachannel hydropathic density variations translate into hydropathic dipole field configurations along the pore. Our findings suggest the existence of a nonrandom cumulative hydropathic topology that is organized parallel to the membrane surface so that pore's stability, as well as, gating behavior are guaranteed. Given the biophysical significance of the hydropathic effect, our study seeks to provide a computational framework for studying cumulative hydropathic topological properties of NavChs and pore-forming proteins in general.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sodium / Bacterial Proteins / Ion Channel Gating / Arcobacter / Voltage-Gated Sodium Channels Type of study: Prognostic_studies Language: En Journal: Proteins Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: Netherlands Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sodium / Bacterial Proteins / Ion Channel Gating / Arcobacter / Voltage-Gated Sodium Channels Type of study: Prognostic_studies Language: En Journal: Proteins Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: Netherlands Country of publication: United States