Human aldehyde oxidase (hAOX1): structure determination of the Moco-free form of the natural variant G1269R and biophysical studies of single nucleotide polymorphisms
| Autor: | Martin Wolff, Cristiano Mota, Mariam Esmaeeli, Silke Leimkühler, Maria João Romão, Catarina Coelho, Alessandro Foti, Teresa Santos-Silva |
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| Přispěvatelé: | DQ - Departamento de Química, UCIBIO - Applied Molecular Biosciences Unit |
| Rok vydání: | 2019 |
| Předmět: |
0301 basic medicine
Models Molecular molybdenum cofactor Population Coenzymes Crystallography X-Ray Polymorphism Single Nucleotide General Biochemistry Genetics and Molecular Biology 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Oxidoreductase single nucleotide polymorphism Metalloproteins Humans education Xanthine oxidase Aldehyde oxidase Research Articles chemistry.chemical_classification education.field_of_study biology Biochemistry Genetics and Molecular Biology(all) Pteridines Active site Cytochrome P450 human aldehyde oxidase Aldehyde Oxidase 030104 developmental biology Biochemistry Xanthine dehydrogenase chemistry 030220 oncology & carcinogenesis biology.protein Molybdenum cofactor Molybdenum Cofactors xanthine oxidase Research Article |
| Zdroj: | FEBS Open Bio 'FEBS Open Bio ', vol: 9, pages: 925-934 (2019) |
| ISSN: | 2211-5463 |
| Popis: | This work was supported by the Applied Molecular Biosciences Unit-UCIBIO which is financed by national funds from FCT/MCTES (UID/Multi/04378/2019), Project PTDC/BBB-BEP/1185/2014 and Grant SFRH/BPD/ 84581/2012 (CC). SL thanks the Deutsche Forschungsge-meinschaft (DFG) for the support with Grant LE1171/8-3. The ESRF staff are also acknowledged, in particular ID30B beamline staff (ESRF, Grenoble). Human aldehyde oxidase (hAOX1) is a molybdenum enzyme with high toxicological importance, but its physiological role is still unknown. hAOX1 metabolizes different classes of xenobiotics and is one of the main drug-metabolizing enzymes in the liver, along with cytochrome P450. hAOX1 oxidizes and inactivates a large number of drug molecules and has been responsible for the failure of several phase I clinical trials. The interindividual variability of drug-metabolizing enzymes caused by single nucleotide polymorphisms (SNPs) is highly relevant in pharmaceutical treatments. In this study, we present the crystal structure of the inactive variant G1269R, revealing the first structure of a molybdenum cofactor (Moco)-free form of hAOX1. These data allowed to model, for the first time, the flexible Gate 1 that controls access to the active site. Furthermore, we inspected the thermostability of wild-type hAOX1 and hAOX1 with various SNPs (L438V, R1231H, G1269R or S1271L) by CD spectroscopy and ThermoFAD, revealing that amino acid exchanges close to the Moco site can impact protein stability up to 10 °C. These results correlated with biochemical and structural data and enhance our understanding of hAOX1 and the effect of SNPs in the gene encoding this enzyme in the human population. Enzymes: Aldehyde oxidase (EC1.2.3.1); xanthine dehydrogenase (EC1.17.1.4); xanthine oxidase (EC1.1.3.2). Databases: Structural data are available in the Protein Data Bank under the accession number 6Q6Q. publishersversion published |
| Databáze: | OpenAIRE |
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