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This Sandbox is Reserved from Jan 13 through September 1, 2020 for use in the course CH462 Biochemistry II taught by R. Jeremy Johnson at the Butler University, Indianapolis, USA. This reservation includes Sandbox Reserved 1598 through Sandbox Reserved 1627.

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Mitochondrial Calcium Uniporter (MCU) (Heumann Test Page)

1 Overview
2 Structure
3 Medical Relevance
4 Regulation and Inhibition

Overview

Article One ^[1] Article Two ^[2] Article Three ^[3] ^[3] Article Four ^[4] Article Five ^[5] ^[5]

The mitochondrial calcium uniporter (MCU) complex is the main source of entry for calcium ions into the mitochondrial matrix from the intermembrane space. MCU channels exist in most eukaryotic life, but activity is regulated differently in each clade.^[2] The precise identity of the MCU wasn't discovered until 2011 and was discovered using a combination of NMR spectroscopy, cryo-electron microscopy, and x-ray crystallography.^[3] Identification of the structure was difficult because it has no apparent sequence similarity to other ion channels.^[2] However, like other ion channels, it is incredibly selective and efficient. The MCU has the ability to only allow calcium ions into the mitochondrial matrix at a rate of 5,000,000 ions per second even though potassium ions are over 100,000 times more abundant in the intermembrane space.^[2]

Under resting conditions, the calcium concentration in the mitochondria is about the same as in the cytoplasm, but when stimulated, it can increase calcium concentration 10-20-fold.^[4] Mitochondria-associated ER membranes (MAMs) exist between mitochondria and the endoplasmic reticulum, the two largest cellular stores of calcium, to allow for efficient transport of calcium ions.^[1] The transfer of electrons through respiratory complexes I-IV produces the energy to pump hydrogen ions into the intermembrane space and create the proton electrochemical gradient potential.^[4] This negative electrochemical potential is the driving force that moves positively charged calcium ions into the mitochondrial matrix.^[4]

Regulation of the uptake and efflux of calcium is important to increase calcium levels enough to activate certain enzymes, but also avoid calcium overload and apoptosis.^[1] Mitochondrial calcium increases ATP production by activating pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and isocitrate dehydrogenase in the Krebs cycle.^[1] Therefore, deficiency of MCU leads to decrease of enzyme activity and of oxidative phosphorylation.

Structure

Mitochondrial Calcium Uniporter Complex

Mitochondrial Calcium Uniporter Structure

Selectivity Filter

Movement of Calcium

Mutations

Medical Relevance

Apoptosis and Cancer

Neurodegenerative Disorders

Diabetes

Regulation and Inhibition

The most well-known and commonly used inhibitor of calcium uptake into the mitochondria is ruthenium red (RuRed). RuRed effectively inhibits calcium uptake without affecting mitochondrial respiration or calcium efflux. Additionally, it has been shown to mitigate tissue damage due to IRI and slow cancer cell migration. The issue with RuRed is that its purification has always been a challenging matter.^[3] Interestingly enough, this led to even more developments in the search for an inhibitor. Many scientists had observed that impure RuRed actually had greater inhibition than pure RuRed. One of the common minor impurities of RuRed, Ru360, was found to be the active component of the RuRed mixtures, meaning it responsible for calcium inhibition. Ru360 is now commercially available and has been widely used for the study of calcium-dependent cellular processes and as a therapeutic agent. Very little is known about its mechanism of inhibtion, but studies show that it interacts with the DXXE motif of the loop connecting the TM1 and TM2 helices.^[3]

Ru360 was a very successful inhibitor, but it showed low cell permeability. So, a new inhibitor called Ru265 was developed which could be easily synthesized and didn't need chromatographic purification. Ru265 had all of the benefits of Ru360, with with twice the cell permeability. Additionally, the same mutations didn't seem to affect it. Mutations of D261 and S259 in human MCU reduced inhibitory effect of Ru360, but not Ru265. Additionally, there were other mutations that affected Ru265, but not Ru360.^[3] This shows how much more research is needed before a mechanism is understood for any inhibitor of the MCU.

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References

↑ ^1.0 ^1.1 ^1.2 ^1.3 Wang CH, Wei YH. Role of mitochondrial dysfunction and dysregulation of Ca(2+) homeostasis in the pathophysiology of insulin resistance and type 2 diabetes. J Biomed Sci. 2017 Sep 7;24(1):70. doi: 10.1186/s12929-017-0375-3. PMID:28882140 doi:http://dx.doi.org/10.1186/s12929-017-0375-3
↑ ^2.0 ^2.1 ^2.2 ^2.3 Baradaran R, Wang C, Siliciano AF, Long SB. Cryo-EM structures of fungal and metazoan mitochondrial calcium uniporters. Nature. 2018 Jul 11. pii: 10.1038/s41586-018-0331-8. doi:, 10.1038/s41586-018-0331-8. PMID:29995857 doi:http://dx.doi.org/10.1038/s41586-018-0331-8
↑ ^3.0 ^3.1 ^3.2 ^3.3 ^3.4 ^3.5 Woods JJ, Wilson JJ. Inhibitors of the mitochondrial calcium uniporter for the treatment of disease. Curr Opin Chem Biol. 2019 Dec 20;55:9-18. doi: 10.1016/j.cbpa.2019.11.006. PMID:31869674 doi:http://dx.doi.org/10.1016/j.cbpa.2019.11.006
↑ ^4.0 ^4.1 ^4.2 ^4.3 Giorgi C, Marchi S, Pinton P. The machineries, regulation and cellular functions of mitochondrial calcium. Nat Rev Mol Cell Biol. 2018 Nov;19(11):713-730. doi: 10.1038/s41580-018-0052-8. PMID:30143745 doi:http://dx.doi.org/10.1038/s41580-018-0052-8
↑ ^5.0 ^5.1 Fan C, Fan M, Orlando BJ, Fastman NM, Zhang J, Xu Y, Chambers MG, Xu X, Perry K, Liao M, Feng L. X-ray and cryo-EM structures of the mitochondrial calcium uniporter. Nature. 2018 Jul 11. pii: 10.1038/s41586-018-0330-9. doi:, 10.1038/s41586-018-0330-9. PMID:29995856 doi:http://dx.doi.org/10.1038/s41586-018-0330-9

Retrieved from "http://52.214.119.220/wiki/index.php/Sandbox_Reserved_1601"

@@ Line 5: / Line 5: @@
 == Overview ==
-Article One <ref name="Wang">PMID:28882140</ref> <ref name="Wang"/>
+Article One <ref name="Wang"/>
-Article Two <ref name="Baradaran">PMID:29995857</ref> <ref name="Baradaran"/>
+Article Two <ref name="Baradaran"/>
 Article Three <ref name="Woods">PMID:31869674</ref> <ref name="Woods"/>
-Article Four <ref name="Giorgi">PMID:30143745</ref> <ref name="Giorgi"/>
+Article Four <ref name="Giorgi"/>
 Article Five <ref name="Fan">PMID:29995856</ref> <ref name="Fan"/>
-Mitochondrial calcium uniporter (MCU) channels exist in most eukaryotic life, but activity is regulated differently in each clade.<ref name="Baradaran">PMID:29995857</ref> The precise identity of the MCU wasn't discovered until 2011 and was discovered using a combination of NMR spectroscopy, cryo-electron microscopy, and x-ray crystallography.<ref name="Woods">PMID:31869674</ref> Identification of the structure was difficult because it has no apparent sequence similarity to other ion channels.<ref name="Baradaran"/> However, like other ion channels, it is incredibly selective and efficient.  The MCU has the ability to only allow Ca^2+ ions
+The mitochondrial calcium uniporter (MCU) complex is the main source of entry for calcium ions into the mitochondrial matrix from the intermembrane space.  MCU channels exist in most eukaryotic life, but activity is regulated differently in each clade.<ref name="Baradaran">PMID:29995857</ref> The precise identity of the MCU wasn't discovered until 2011 and was discovered using a combination of NMR spectroscopy, cryo-electron microscopy, and x-ray crystallography.<ref name="Woods">PMID:31869674</ref> Identification of the structure was difficult because it has no apparent sequence similarity to other ion channels.<ref name="Baradaran"/> However, like other ion channels, it is incredibly selective and efficient.  The MCU has the ability to only allow calcium ions into the mitochondrial matrix at a rate of 5,000,000 ions per second even though potassium ions are over 100,000 times more abundant in the intermembrane space.<ref name="Baradaran"/>
+Under resting conditions, the calcium concentration in the mitochondria is about the same as in the cytoplasm, but when stimulated, it can increase calcium concentration 10-20-fold.<ref name="Giorgi">PMID:30143745</ref>  Mitochondria-associated ER membranes (MAMs) exist between mitochondria and the endoplasmic reticulum, the two largest cellular stores of calcium, to allow for efficient transport of calcium ions.<ref name="Wang">PMID:28882140</ref>  The transfer of electrons through respiratory complexes I-IV produces the energy to pump hydrogen ions into the intermembrane space and create the proton electrochemical gradient potential.<ref name="Giorgi"/> This negative electrochemical potential is the driving force that moves positively charged calcium ions into the mitochondrial matrix.<ref name="Giorgi"/>
+Regulation of the uptake and efflux of calcium is important to increase calcium levels enough to activate certain enzymes, but also avoid calcium overload and apoptosis.<ref name="Wang"/> Mitochondrial calcium increases ATP production by activating pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, and isocitrate dehydrogenase in the Krebs cycle.<ref name="Wang"/>  Therefore, deficiency of MCU leads to decrease of enzyme activity and of oxidative phosphorylation.
 ==Structure==