Structures of a sperm-specific solute carrier gated by voltage and cAMP

• Verfasst von: Kalienkova, Valeria [VerfasserIn]
• Verfasst von: Peter, Martin F. [VerfasserIn]
• Verfasst von: Rheinberger, Jan [VerfasserIn]
• Verfasst von: Batista Paulino, Cristina [VerfasserIn]
• Titel: Structures of a sperm-specific solute carrier gated by voltage and cAMP
• Verf.angabe: Valeria Kalienkova, Martin F. Peter, Jan Rheinberger, Cristina Paulino
• E-Jahr: 2023
• Jahr: 25 October 2023
• Umfang: 8 S.
• Fussnoten: Gesehen am 16.11.2023
• Titel Quelle: Enthalten in: Nature <London>
• Ort Quelle: London [u.a.] : Nature Publ. Group, 1869
• Jahr Quelle: 2023
• Band/Heft Quelle: 623(2023), 7985, Seite 202-209
• ISSN Quelle: 1476-4687
• DOI: doi:10.1038/s41586-023-06629-w
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Cryoelectron microscopy
• Sach-SW: Membrane proteins
• Sach-SW: Molecular conformation
• K10plus-PPN: 187043871X

Abstract

The newly characterized sperm-specific Na+/H+ exchanger stands out by its unique tripartite domain composition1,2. It unites a classical solute carrier unit with regulatory domains usually found in ion channels, namely, a voltage-sensing domain and a cyclic-nucleotide binding domain1,3, which makes it a mechanistic chimera and a secondary-active transporter activated strictly by membrane voltage. Our structures of the sea urchin SpSLC9C1 in the absence and presence of ligands reveal the overall domain arrangement and new structural coupling elements. They allow us to propose a gating model, where movements in the voltage sensor indirectly cause the release of the exchanging unit from a locked state through long-distance allosteric effects transmitted by the newly characterized coupling helices. We further propose that modulation by its ligand cyclic AMP occurs by means of disruption of the cytosolic dimer interface, which lowers the energy barrier for S4 movements in the voltage-sensing domain. As SLC9C1 members have been shown to be essential for male fertility, including in mammals2,4,5, our structure represents a potential new platform for the development of new on-demand contraceptives.