Counterintuitive structural and functional effects due to naturally occurring mutations targeting the active site of the disease‐associated NQO1 enzyme. (25th November 2022)

• Record Type: Journal Article
• Authors: Pacheco‐García, Juan Luis; Anoz‐Carbonell, Ernesto; Loginov, Dmitry S.; Kavan, Daniel; Salido, Eduardo; Man, Petr; Medina, Milagros; Pey, Angel L.
• Is Part Of: FEBS journal. Volume 290:Number 7(2023)
• Page Start: 1855
• Page End: 1873
• Publication Date: 2022-11-25
• Subjects: catalytic mechanism -- genotype–phenotype correlations -- protein structure–function -- structural stability; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Pathology, Molecular -- Periodicals; 572
• DOI: 10.1111/febs.16677
• Languages: English
• ISSNs: 1742-464X

Abstract

Abstract : Our knowledge on the genetic diversity of the human genome is exponentially growing. However, our capacity to establish genotype–phenotype correlations on a large scale requires a combination of detailed experimental and computational work. This is a remarkable task in human proteins which are typically multifunctional and structurally complex. In addition, mutations often prevent the determination of mutant high‐resolution structures by X‐ray crystallography. We have characterized here the effects of five mutations in the active site of the disease‐associated NQO1 protein, which are found either in cancer cell lines or in massive exome sequencing analysis in human population. Using a combination of H/D exchange, rapid‐flow enzyme kinetics, binding energetics and conformational stability, we show that mutations in both sets may cause counterintuitive functional effects that are explained well by their effects on local stability regarding different functional features. Importantly, mutations predicted to be highly deleterious (even those affecting the same protein residue) may cause mild to catastrophic effects on protein function. These functional effects are not well explained by current predictive bioinformatic tools and evolutionary models that account for site conservation and physicochemical changes upon mutation. Our study also reinforces the notion that naturally occurring mutations not identified as disease‐associated can be highly deleterious. Our approach, combining protein biophysics and structural biology tools, is readily accessible to broadly increase our understanding of genotype–phenotype correlations and to improve predictive computational tools aimed at distinguishing disease‐prone against neutral missense variants in the human genome. Abstract : Genetic diversity in the human genome has unknown effects on protein function and disease propensity. Mutations in active sites are expected to have large effects on enzyme function. We characterized here five naturally occurring mutations targeting the active site of the cancer‐associated NQO1 enzyme. Mutational effects are rationalized only when these are structurally analysed in different catalytically relevant states. We propose new concepts to improve large‐scale predictors of genotype–phenotype relationships.