Abstract
BackgroundPredicting the effect of single point variations on protein stability constitutes a crucial step toward understanding the relationship between protein structure and function. To this end, several methods have been developed to predict changes in the Gibbs free energy of unfolding (∆∆G) between wild type and variant proteins, using sequence and structure information. Most of the available methods however do not exhibit the anti-symmetric prediction property, which guarantees that the predicted ∆∆G value for a variation is the exact opposite of that predicted for the reverse variation, i.e., ∆∆G(A → B) = −∆∆G(B → A), where A and B are amino acids.ResultsHere we introduce simple anti-symmetric features, based on evolutionary information, which are combined to define an untrained method, DDGun (DDG untrained). DDGun is a simple approach based on evolutionary information that predicts the ∆∆G for single and multiple variations from sequence and structure information (DDGun3D). Our method achieves remarkable performance without any training on the experimental datasets, reaching Pearson correlation coefficients between predicted and measured ∆∆G values of ~ 0.5 and ~ 0.4 for single and multiple site variations, respectively. Surprisingly, DDGun performances are comparable with those of state of the art methods. DDGun also naturally predicts multiple site variations, thereby defining a benchmark method for both single site and multiple site predictors. DDGun is anti-symmetric by construction predicting the value of the ∆∆G of a reciprocal variation as almost equal (depending on the sequence profile) to -∆∆G of the direct variation. This is a valuable property that is missing in the majority of the methods.ConclusionsEvolutionary information alone combined in an untrained method can achieve remarkably high performances in the prediction of ∆∆G upon protein mutation. Non-trained approaches like DDGun represent a valid benchmark both for scoring the predictive power of the individual features and for assessing the learning capability of supervised methods.
Highlights
Predicting the effect of single point variations on protein stability constitutes a crucial step toward understanding the relationship between protein structure and function
The three following scores are based purely on sequence data: 1. the difference between the wild type and mutant residue in the Blosum62 substitution matrix; 2. the difference in the interaction energy between the wild-type and substituted residue with their sequence neighbours within a 2-residue window; 3. the difference in the hydrophobicity between wild type and mutant residues according to the Kyte-Doolittle scale
We need predictors that can be as good as predicting protein stability changes upon variations and at the same time obtaining opposite values for the reciprocal sequence changes that bring the mutated proteins back to their respective wild types
Summary
Predicting the effect of single point variations on protein stability constitutes a crucial step toward understanding the relationship between protein structure and function. To this end, several methods have been developed to predict changes in the Gibbs free energy of unfolding (ΔΔG) between wild type and variant proteins, using sequence and structure information. Structure-based methods take advantage of the features representing the structural environment of the substituted residue. The combination of such features with physical and statistical potentials, improves the performance of the predictors [2]. In general, sequencebased predictors are less accurate than structure-based ones, some sequence-based methods, especially those exploiting evolutionary information, show comparable performances to structure-based tools [20]
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