Mitochondrial calcium uniporter
Identifiers
SymbolMCU
PfamPF04678
InterProIPR018782
TCDB1.A.77
OPM superfamily486
OPM protein6dnf
Membranome216
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary
Mitochondrial calcium uniporter
Identifiers
SymbolMCU
Alt. symbolsC10orf42, CCDC109A, FLJ46135
NCBI gene90550
HGNC23526
OMIM614197
PDBQ8NE86
RefSeqNM_138357
UniProtQ8NE86
Other data
LocusChr. 10 222
Search for
StructuresSwiss-model
DomainsInterPro

The mitochondrial calcium uniporter (MCU) is a transmembrane protein that allows the passage of calcium ions from a cell's cytosol into mitochondria. Its activity is regulated by MICU1 and MICU2, which together with the MCU make up the mitochondrial calcium uniporter complex.[1]

The MCU is one of the primary sources of mitochondria uptake of calcium, and flow is dependent on membrane potential of the inner mitochondrial membrane and the concentration of calcium in the cytosol relative to the concentration in the mitochondria. Balancing calcium concentration is necessary to increase the cell's energy supply and regulate cell death. Calcium is balanced through the MCU in conjunction with the sodium-calcium exchanger.

The MCU has a very low affinity for calcium, so the cytosolic calcium concentration needs to be approximately 5-10 uM for significant transport of calcium into the mitochondria. Mitochondria are closely associated with the endoplasmic reticulum (ER), at contact sites, which contains stores of cellular calcium ions for calcium signaling. The presence of 1,4,5-triphosphate (IP3) triggers the release of calcium from these intracellular stores, which creates microdomains of high calcium concentration between the ER and the mitochondria, creating the conditions for the MCU to take up calcium.[2]

Ruthenium red and Ru360 are typical reagents used to experimentally block the MCU to study its properties and role in mitochondrial signaling.[3][4]

MICU1 and MICU2

MICU1

The mitochondrial calcium uptake 1 (MICU1) is a single pass membrane protein, it contains 2 binding domains. This protein was first discovered before the MCU by only a few months. MICU1 was used as a bait to figure out what the core of the mitochondrial calcium uniporter was.[2] Once both MICU1 and MCU were discovered scientists made some intriguing discoveries in regards to the two proteins. Both MICU1 and MCU share similar RNA sequences, same pattern of expression, and they both interact with one another in the intermitochondrial membrane. It was first found through the use of siRNA screening of the membrane. The functions of MICU1 are still being studied; however, there are some important functions MICU1 plays in the intermitochondrial membrane. MICU1 helps to stabilize the entire mitochondrial calcium uniporter complex, it also limits the amount of calcium that enters the cell during low concentrations of calcium. However, along with limiting the entry of calcium into the mitochondrial matrix, it functions alongside MCU to keep the accumulated calcium inside the matrix of the mitochondria,[2] and promotes ion specificity by preventing aberrant loading of transition metals into the mitochondria. [5][6][7]

MICU2

Mitochondrial calcium uptake 2 (MICU2) is another intermitochondrial membrane protein. It works alongside MICU1 and contains roughly 25% of the same DNA sequence.[2] MICU2 works with MICU1 and MCU to reduce the amount of calcium coming into the matrix. It is shown that when both MICU1 and MICU2 are sequestered there is reduced calcium; however, whenever MICU1 is sequestered and MICU2 is activated, normal calcium flow. It is also shown that all three, MCU, MICU1, and MICU2 are part of a single complex, the mitochondrial calcium uniporter complex resumes.[2] Research using a CRISPR/Cas9 technique has found that MICU1 and MICU2 play other roles as well. They are essential for cell growth, cell invasion, and cell replication.

References

  1. ^ "MCU - Calcium uniporter protein, mitochondrial precursor - Homo sapiens (Human)". UniProt.org. UniProt Consortium. Retrieved 2016-02-24.
  2. ^ a b c d e Marchi S, Pinton P (March 2014). "The mitochondrial calcium uniporter complex: molecular components, structure and physiopathological implications". The Journal of Physiology. 592 (5): 829–839. doi:10.1113/jphysiol.2013.268235. PMC 3948548. PMID 24366263.
  3. ^ Broekemeier KM, Krebsbach RJ, Pfeiffer DR (October 1994). "Inhibition of the mitochondrial Ca2+ uniporter by pure and impure ruthenium red". Molecular and Cellular Biochemistry. 139 (1): 33–40. doi:10.1007/bf00944201. PMID 7531818. S2CID 516473.
  4. ^ Matlib MA, Zhou Z, Knight S, Ahmed S, Choi KM, Krause-Bauer J, et al. (April 1998). "Oxygen-bridged dinuclear ruthenium amine complex specifically inhibits Ca2+ uptake into mitochondria in vitro and in situ in single cardiac myocytes". The Journal of Biological Chemistry. 273 (17): 10223–10231. doi:10.1074/jbc.273.17.10223. PMID 9553073.
  5. ^ Kamer KJ, Sancak Y, Fomina Y, Meisel JD, Chaudhuri D, Grabarek Z, Mootha VK (August 2018). "MICU1 imparts the mitochondrial uniporter with the ability to discriminate between Ca2+ and Mn2+". Proceedings of the National Academy of Sciences of the United States of America. 115 (34): E7960–E7969. doi:10.1073/pnas.1807811115. PMC 6112746. PMID 30082385.
  6. ^ Wettmarshausen J, Goh V, Huang KT, Arduino DM, Tripathi U, Leimpek A, et al. (November 2018). "MICU1 Confers Protection from MCU-Dependent Manganese Toxicity" (PDF). Cell Reports. 25 (6): 1425–1435.e7. doi:10.1016/j.celrep.2018.10.037. PMID 30403999. S2CID 53209158.
  7. ^ Monteith AJ, Miller JM, Beavers WN, Maloney KN, Seifert EL, Hajnoczky G, Skaar EP (December 2021). "Mitochondrial calcium uniporter affects neutrophil bactericidal activity during Staphylococcus aureus infection". Infection and Immunity. 90 (2): IAI0055121. doi:10.1128/IAI.00551-21. PMC 8853686. PMID 34871043.
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