Calcium regulation of the human mitochondrial ATP-Mg/Pi carrier SLC25A24 uses a locking pin mechanism


Type
Article
Change log
Authors
Harborne, SPD 
King, MS 
Crichton, PG 
Kunji, ERS 
Abstract

Mitochondrial ATP-Mg/Pi carriers import adenine nucleotides into the mitochondrial matrix and export phosphate to the cytosol. They are calcium-regulated to control the size of the matrix adenine nucleotide pool in response to cellular energetic demands. They consist of three domains: an N-terminal regulatory domain containing four calcium-binding EF-hands, a linker loop domain with an amphipathic α-helix and a C-terminal mitochondrial carrier domain for the transport of substrates. Here, we use thermostability assays to demonstrate that the carrier is regulated by calcium via a locking pin mechanism involving the amphipathic α-helix. When calcium levels in the intermembrane space are high, the N-terminus of the amphipathic α-helix is bound to a cleft in the regulatory domain, leading to substrate transport by the carrier domain. When calcium levels drop, the cleft closes, and the amphipathic α-helix is released to bind to the carrier domain via its C-terminus, locking the carrier in an inhibited state.

Description
Keywords
enzyme mechanisms, structural biology
Journal Title
Scientific Reports
Conference Name
Journal ISSN
2045-2322
2045-2322
Volume Title
7
Publisher
Nature Publishing Group
Sponsorship
Medical Research Council (MC_U105663139)
Biotechnology and Biological Sciences Research Council (BB/R50564X/1)
Medical Research Council (MC_UU_00015/1)