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Structural Insights into the Iodothyronine Deiodinase 2 Catalytic Core and Deiodinase Catalysis and Dimerization

Overview
Journal Biomolecules
Publisher MDPI
Date 2024 Nov 27
PMID 39595550
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Abstract

Iodothyronine deiodinases (Dio) are selenocysteine-containing membrane enzymes that activate and inactivate the thyroid hormones (TH) through reductive iodide eliminations. The three deiodinase isoforms are homodimers sharing highly conserved amino acid sequences, but they differ in their regioselectivities for the deiodination reaction and regulatory features. We have now solved a crystal structure of the mouse deiodinase 2 (Dio2) catalytic domain. It reveals a high overall similarity to the deiodinase 3 structure, supporting the proposed common mechanism, but also Dio2-specific features, likely mediating its unique properties. Activity studies with an artificially enforced Dio dimer further confirm that dimerization is required for activity and requires both the catalytic core and the enzyme's N-terminus. Cross-linking studies reveal the catalytic core's dimerization interface, providing insights into the architecture of the complete, active Dio homodimer.

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References
1.
Callebaut I, Curcio-Morelli C, Mornon J, Gereben B, Buettner C, Huang S . The iodothyronine selenodeiodinases are thioredoxin-fold family proteins containing a glycoside hydrolase clan GH-A-like structure. J Biol Chem. 2003; 278(38):36887-96. DOI: 10.1074/jbc.M305725200. View

2.
Koehrle J, Aufmkolk M, Rokos H, Hesch R, Cody V . Rat liver iodothyronine monodeiodinase. Evaluation of the iodothyronine ligand-binding site. J Biol Chem. 1986; 261(25):11613-22. View

3.
Marsili A, Zavacki A, Harney J, Larsen P . Physiological role and regulation of iodothyronine deiodinases: a 2011 update. J Endocrinol Invest. 2011; 34(5):395-407. PMC: 3687787. DOI: 10.1007/BF03347465. View

4.
Berry M, Maia A, Kieffer J, Harney J, Larsen P . Substitution of cysteine for selenocysteine in type I iodothyronine deiodinase reduces the catalytic efficiency of the protein but enhances its translation. Endocrinology. 1992; 131(4):1848-52. DOI: 10.1210/endo.131.4.1396330. View

5.
Adams P, Afonine P, Bunkoczi G, Chen V, Davis I, Echols N . PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr D Biol Crystallogr. 2010; 66(Pt 2):213-21. PMC: 2815670. DOI: 10.1107/S0907444909052925. View