The stability of G6PD is affected by mutations with different clinical phenotypes

• Published in: International journal of molecular sciences Vol. 15; no. 11; pp. 21179 - 21201
• Main Authors: Gómez-Manzo, Saúl, Terrón-Hernández, Jessica, De la Mora-De la Mora, Ignacio, González-Valdez, Abigail, Marcial-Quino, Jaime, García-Torres, Itzhel, Vanoye-Carlo, America, López-Velázquez, Gabriel, Hernández-Alcántara, Gloria, Oria-Hernández, Jesús, Reyes-Vivas, Horacio, Enríquez-Flores, Sergio
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 17.11.2014; MDPI
• Subjects: Enzyme Stability; Enzymes; G6PD-deficient E. coli; Genotype & phenotype; glucose-6-phosphate dehydrogenase (G6PD) deficiency; Glucosephosphate Dehydrogenase - chemistry; Glucosephosphate Dehydrogenase - genetics; Glucosephosphate Dehydrogenase - metabolism; Glucosephosphate Dehydrogenase Deficiency - enzymology; Glucosephosphate Dehydrogenase Deficiency - genetics; Humans; Models, Molecular; Mutation; Phenotype; Protein Conformation; Protein expression; protein stability; recombinant G6PD enzymes; Recombinant Proteins - chemistry; Recombinant Proteins - genetics; Recombinant Proteins - metabolism; structural characterization; structural NADP; Temperature; thermostability; variants
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms151121179

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzyme deficiency worldwide, causing a wide spectrum of conditions with severity classified from the mildest (Class IV) to the most severe (Class I). To correlate mutation sites in the G6PD with the resulting phenotypes, we studied four naturally occurring G6PD variants: Yucatan, Nashville, Valladolid and Mexico City. For this purpose, we developed a successful over-expression method that constitutes an easier and more precise method for obtaining and characterizing these enzymes. The k(cat) (catalytic constant) of all the studied variants was lower than in the wild-type. The structural rigidity might be the cause and the most evident consequence of the mutations is their impact on protein stability and folding, as can be observed from the protein yield, the T50 (temperature where 50% of its original activity is retained) values, and differences on hydrophobic regions. The mutations corresponding to more severe phenotypes are related to the structural NADP+ region. This was clearly observed for the Classes III and II variants, which became more thermostable with increasing NADP+, whereas the Class I variants remained thermolabile. The mutations produce repulsive electric charges that, in the case of the Yucatan variant, promote increased disorder of the C-terminus and consequently affect the binding of NADP+, leading to enzyme instability.