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Defensin^[1]

Defensin

Texte

Structure

Defensin

Each monomer is divided in : , and the domains. Each of these has a regular structure: a surrounded by .^[2] 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.^[3] Finally, the C-term Asp-rich end is intrisically disordered (therefore, the C-term end cannot be represented in 3D structures). ^[4]

Polymer Structure

Within the sarcoplasmic reticulum (SR) lumen, CASQ2 polymerizes to form , homotetramers and . There are two forms of dimerization: the and the .^[5] The front-to-front one is stabilized by intermolecular interactions between the of each CASQ2.^[5] The intermolecular salt bridges are built between .^[5] 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 348 and Glu 350 for the second one.^[5]

The back-to-back form is stabilized by intermolecular interactions between the , ^[5], and it has also been proved that the is involved^[6] (). The intermolecular salt bridges are built between Glu 215 and Lys 86, Glu 216 and Lys 24, Glu 169 and Lys 85.^[5] 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⁺.^[5]

Calcium Binding

Each monomere of CASQ2 can bind between . The Ca²⁺ ions bind to two or more acidic amino acids like or . These amino acids are mainly oriented outside and in the C-terminal region. It had been shown that Ca²⁺ions mainly bind 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 and dimer interactions.^[7]

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.^[8]

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.^[9] Triadin and juctin can bind to CASQ2 on their KEKE motifs (amino acids 210-224 in the triadin chain).^[9] Both proteins bind CASQ2 on its Asp-rich region of the C-terminal region.^[9] Triadin and Junctin can also interact with Ryanodin Receptor.^[9] The binding site of CASQ2 to Ryanodin Receptor (RyR) is unknown.^[9]

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.^[8] CASQ2 is free when the concentration of Ca²⁺ is higher than 1 mM in the SR lumen.^[9]

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).^[8] 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.^[8] The consensus sequence recognized by CK II is Ser/Thr-X-X-Asp/Glu.^[8] The phosphorylation is more likely if there are acidic residues after this consensus sequence.^[8]

The phosphorylation and dephosphorylation of CASQ2 may provide an off/on switch for CASQ2 to regulate Ca²⁺ capture. But there is not any proof yet.^[8] However it is known that phosphorylations on CASQ2 modify the interactions between CASQ2 and RyR but not between CASQ2 and Triadin and Junctin.^[8]