Structural and interaction analysis of monomeric 14-3-3ζ phosphorylated at Ser58 by NMR spectroscopy

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Publikace nespadá pod Ústav výpočetní techniky, ale pod Přírodovědeckou fakultu. Oficiální stránka publikace je na webu muni.cz.
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KOZELEKOVÁ Aneta CRHA Radek VAŘEČKA Vojtěch BROM Tomáš VOLKO Viliam KUTÝ Ondřej HRITZ Jozef

Rok publikování 2026
Druh Recenzovaný odborný článek
Časopis / Zdroj International Journal of Biological Macromolecules
Fakulta / Pracoviště MU

Přírodovědecká fakulta

Citace
www https://www.sciencedirect.com/science/article/pii/S0141813026033234?via%3Dihub
Doi https://doi.org/10.1016/j.ijbiomac.2026.153383
Klíčová slova 14-3-3 zeta monomer; C-terminus mobility; N-terminus destabilization; NMR assignment; Phosphorylation; Secondary interaction site; Tau
Přiložené soubory
Popis 14-3-3 proteins are important dimeric regulatory proteins in the human body that bind phosphorylated partners and regulate their activity. Phosphorylation of 14-3-3 proteins at S58 (pS58) at the dimeric interface was shown to trigger their monomerization and change their thermal stability, hydrophobicity, binding affinity and stoichiometry. However, the direct effect of phosphorylation and monomerization on 14-3-3 structure remains poorly understood. Here, we employed solution nuclear magnetic resonance (NMR) spectroscopy to elucidate the structural features of monomeric 14-3-3? pS58 protein and its interaction with (phospho)Tau protein variants with single-residue resolution. First, based on the NMR assignment and calculated secondary structure propensities, we revealed that the phosphorylation and monomerization decrease helical propensity of the ?C and ?D helices. Second, using NMR titration experiments, we identified two secondary interaction sites (SISs) on 14-3-3? protein outside of the binding groove – one located at the end of ?C helix and another in the loop connecting the ?H and ?I helices. Third, paramagnetic relaxation enhancement experiments showed which 14-3-3? regions are approached by its flexible C-terminus. Importantly, these regions overlap with the SISs but not the binding groove, providing an alternative explanation for the autoinhibitory function of the C-terminus. Taken together, we report novel insight into the structure and interactions of monomeric 14-3-3, connected with S58 phosphorylation.
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