High-resolution crystal structures leverage protein binding affinity predictions

Proteins. 2016 Jan;84(1):9-20. doi: 10.1002/prot.24946. Epub 2015 Nov 23.


Predicting protein binding affinities from structural data has remained elusive, a difficulty owing to the variety of protein binding modes. Using the structure-affinity-benchmark (SAB, 144 cases with bound/unbound crystal structures and experimental affinity measurements), prediction has been undertaken either by fitting a model using a handfull of predefined variables, or by training a complex model from a large pool of parameters (typically hundreds). The former route unnecessarily restricts the model space, while the latter is prone to overfitting. We design models in a third tier, using 12 variables describing enthalpic and entropic variations upon binding, and a model selection procedure identifying the best sparse model built from a subset of these variables. Using these models, we report three main results. First, we present models yielding a marked improvement of affinity predictions. For the whole dataset, we present a model predicting Kd within 1 and 2 orders of magnitude for 48% and 79% of cases, respectively. These statistics jump to 62% and 89% respectively, for the subset of the SAB consisting of high resolution structures. Second, we show that these performances owe to a new parameter encoding interface morphology and packing properties of interface atoms. Third, we argue that interface flexibility and prediction hardness do not correlate, and that for flexible cases, a performance matching that of the whole SAB can be achieved. Overall, our work suggests that the affinity prediction problem could be partly solved using databases of high resolution complexes whose affinity is known.

Keywords: atomic packing; binding affinity prediction; high resolution crystallography; linear regression; protein flexibility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Crystallography, X-Ray
  • Databases, Protein
  • Humans
  • Models, Biological
  • Models, Molecular
  • Protein Binding
  • Protein Conformation
  • Proteins / chemistry*
  • Proteins / metabolism*
  • Thermodynamics


  • Proteins