Sandbox Reserved 820

This Sandbox is Reserved from 06/12/2018, through 30/06/2019 for use in the course "Structural Biology" taught by Bruno Kieffer at the University of Strasbourg, ESBS. This reservation includes Sandbox Reserved 1480 through Sandbox Reserved 1543.

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spinqualitylabelsall models Crystal Structure of Human Cardiac Calsequestrin, (PDB code 2vaf) Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Calsequestrin-2 (or CASQ2) is the soluble Ca2+ binding protein in the sarcoplasmic reticulum lumen of the cardiac muscle cells. CASQ2 could be either in a monomeric, homodimeric, or homooligomeric chain form depending on its bounds with Ca2+. Mutations of CASQ2 are involved in cardiac diseases such as Catecholaminergic Polymorphic Ventricular Tachycardia. Calsequestrin in the calcium cycle of myocyte contraction Biological role The contractions of cardiac myocytes are triggered by the increase of calcium concentration in the cytosol. This phenomenon is highly controlled at several levels. First the calcium is stocked in a cell compartment called the sarcoplasmic reticulum. Then the release of calcium in the cytosol is dependent of the myocytes membrane depolarization. Finally the release of calcium is extremely brief, as soon as the depolarization is over, the calcium is actively pumped in the sarcoplasmic reticulum. The calsequestrin 2 plays a major role here, because it regulates the release of the calcium in the cytosol while the membrane depolarization occurs and traps the calcium inside the lumen of the sarcoplasmic reticulum. It is also good to notice that a huge release of calcium in the cytosol would be lethal to the cell, since the calcium would precipitate with the free phosphate groups. Structure Monomere Structure Each monomer is divided in 3 thioredoxin domains (TRX): the N-term, the middle and the C-term domains. Each of these has a regular structure: a 5 strands beta sheet core surrounded by 4 alpha helices. Usually these domains are involved in redox phenomena, which lead to disulfide bounds creation. Here these domains are inactive but play an important role in the polymerization of CASQ2. Finally, the C-term Asp-rich end is intrisically disordered (therefore, the C-term end cannot be represented in 3D structures). Polymer Structure Within the sarcoplasmic reticulum (SR) lumen, CASQ2 polymerizes to form homodimers, homotetramers and homooligomers. There are two types of dimerization: the front-to-front form and the back-to-back form. The front-to-front form is stabilized by intermolecular interactions between the α2 helix of the domain I of each CASQ2. The intermolecular salt bridges are built between Glu 55 and Lys 49. This dimerization induces the formation of an electronegative pocket which involves the following amino acids: Glu 39, Glu 54, Glu 78, Glu 92, Asp 93 and Asp 101 for the first monomere and Glu 199, Asp 245, Asp 278, Glu 350 and Glu 348 for the second one. The back-to-back form is stabilized by intermolecular interactions between the α3 helix of the domain I, α4 helix of the domain II, and it has also been proved that the C-term domain is involved (together). The intermolecular salt bridges are built between Glu 215 and Lys 86, Glu 216 and Lys 24, Glu 169 and Lys 85. The dimerization is also favored by a hydrogen bond between Ala 82 and Asn 22. This dimerization creates a very electronegative pocket at the C-terminal region which enables the binding of Ca2+. Calcium Binding Each monomere of CASQ2 can bind between 18 to 50 Ca2+. The Ca2+ ions bind to two or more acidic amino acids like Glutamate or Aspartate. These amino acids are mainly oriented outside and in the C-terminal region. It had been shown that Ca2+ions mainly binds an Asp-rich region on the disordered C-terminal domain. When CASQ2 form homooligomers, Ca2+ can be bound in the electronegative pockets created by the front-to-front and back-to-back dimer interactions. CASQ2 can also bind other ions like Mg2+ or H+. The affinity for Mg2+ is lower than the affinity for Ca2+ however the concentration of Ca2+ decreases. When the pH is low, the calcium-binding capacity of CASQ2 decreases as H+ ions occupy the acidic sites and inhibit the polymerization. Interaction between CASQ2, Junctin and Triadin Binding sites CASQ2 can be anchored into the membrane of SR thanks to two integral proteins: the triadin and the junctin. Triadin and juctin can bind to CASQ2 on their KEKE motifs (amino acids 210-224 in the triadin chain). Both proteins bind CASQ2 on its Asp-rich region of the C-terminal region. Triadin and Junctin can also interact with Ryanodin Receptor. The binding site of CASQ2 to Ryanodin Receptor (RyR) is unknow. Consequences of CASQ2 binding CASQ2 and the regulation of Ca2+ release in the cytoplasm. When CASQ2 binds to triadin and junctin, it induces the inhibition of RyR and then the inhibition of calcium release in the cytoplasm. On the contrary, when CASQ2 unbinds triadin and junctin, it induces the activation of Ryr and an efflux of Ca2+ from the SR to the cytoplasm. CASQ2 is free when the concentration of Ca2+ is higher than 1 mM in the SR lumen. Posttranslational modifications of CASQ2 CASQ2 can be phosphorylated by three different kinases: casein kinase I (CK I), casein kinase II (CK II) and ε protein kinase C1 (εPKC1). CK II is located in the SR and is able to phosphorylate Ser 378, Ser 382 and Ser 386. These residues are on the C-terminal domain. The consensus sequence recognized by CK II is Ser/Thr-X-X-Asp/Glu. The phosphorylation is more likely if there are acidic residues after this consensus sequence. The phosphorylation and de-phosphorylation of CASQ2 may provide an off/on switch for CASQ2 to regulate Ca2+ capture. But there is not any proof yet. However it is known that phosphorylations on CASQ2 modify the interactions between CASQ2 and RyR but not between CASQ2 and Triadin and Junctin.

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