Molecular mechanisms of SLC30A10-mediated manganese transport

Nat Commun. 2025 Sep 29;16(1):8581. doi: 10.1038/s41467-025-63616-7.

Abstract

Manganese ion (Mn²⁺) is crucial for various physiological processes, yet excessive levels disrupt cellular homeostasis and impair the function of multiple organelles. The transporter SLC30A10 plays a pivotal role in Mn²⁺ homeostasis by exporting Mn²⁺ from cells, preventing toxic effects. Mutations in the SLC30A10 gene result in Mn²⁺ accumulation and lead to disorders such as hypermanganesemia with dystonia 1 (HMNDYT1). Despite its physiological significance, the structural basis underlying Mn²⁺ binding and the detailed transport mechanisms of SLC30A10 remain unknown. Here, we present diverse conformations of high-resolution cryo-electron microscopy (cryo-EM) structures that reveal a Mn²⁺-binding site in SLC30A10, setting it apart from other SLC30 family transporters. Furthermore, we show that the HMNDYT1-associated D40A mutation interrupts Mn²⁺ binding and transport, identifying D40 as a potential therapeutic target. These findings provide structural insights into Mn²⁺ transport mechanisms mediated by SLC30A10, advancing our understanding of Mn²⁺ binding and potential targets for future therapeutic exploration.

MeSH terms

  • Binding Sites
  • Biological Transport
  • Cation Transport Proteins* / chemistry
  • Cation Transport Proteins* / genetics
  • Cation Transport Proteins* / metabolism
  • Cation Transport Proteins* / ultrastructure
  • Cryoelectron Microscopy
  • HEK293 Cells
  • Humans
  • Ion Transport
  • Manganese* / metabolism
  • Models, Molecular
  • Mutation
  • Protein Binding
  • Zinc Transporter 8

Substances

  • Manganese
  • Cation Transport Proteins
  • SLC30A10 protein, human
  • Zinc Transporter 8