High-affinity cooperative Ca2+ binding by MICU1- MICU2 serves as an on-off switch for the uniporter.

The mitochondrial calcium uniporter is a Ca²⁺-activated Ca²⁺ channel that is essential for dynamic modulation of mitochondrial function in response to cellular Ca²⁺ signals. It is regulated by two paralogous EF-hand proteins- MICU1 and MICU2, but the mechanism is unknown. Here, we demonstrate that both MICU1 and MICU2 are stabilized by Ca²⁺. We reconstitute the MICU1- MICU2 heterodimer and demonstrate that it binds Ca²⁺ cooperatively with high affinity. We discover that both MICU1 and MICU2 exhibit affinity for the mitochondria-specific lipid cardiolipin. We determine the minimum Ca²⁺ concentration required for disinhibition of the uniporter in permeabilized cells and report a close match with the Ca²⁺-binding affinity of MICU1- MICU2. We conclude that cooperative, high-affinity interaction of the MICU1- MICU2 complex with Ca²⁺ serves as an on-off switch, leading to a tightly controlled channel, capable of responding directly to cytosolic Ca²⁺ signals. [ABSTRACT FROM AUTHOR]