Making a fast ion transporter
Na+/H+ antiporters exchange sodium ions and protons across cellular membrane to control pH, ion concentrations and cell volume, which is linked to a wide spectrum of diseases from heart failure to autism. Researchers now design a faster Na+/H+ antiporter based on the simulations.
An international team of researchers, research associate professor Kei-ichi Okazaki at Institute for Molecular Science and groups of professors Gerhard Hummer and Werner Kühlbrandt at Max Planck Institute of Biophysics, revealed an ion transport mechanism of the archaeal Na+/H+ antiporter PaNhaP in atomic detail by molecular dynamics simulations. Based on the simulations, they discovered a pair of residues that serves as a gate to the ion-binding site. Furthermore, they found that a mutation weakening the gate makes the transporter twice as fast as the wild type. The work was published in Nature Communications on April 15, 2019.
“It was surprising that the mutation makes the transporter faster,” Okazaki says, “the speed-up suggests that the gate balances competing demands of fidelity and efficiency.” The gate was discovered through simulations where they applied a method called transition path sampling to overcome the enormous time-scale gap between seconds-scale ion exchange and microseconds simulations. The simulations captured the ion transporting events, which is not possible with conventional simulations.
“We would like to understand design principles of transporters, how they recognize their substrates and how they control transport speeds,” Okazaki says, “these mechanistic understandings can help develop drugs to cure transporter-related diseases in future.”
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