A new Lamarckian genetic algorithm for flexible ligand-receptor docking

J Comput Chem. 2010 Jul 15;31(9):1911-8. doi: 10.1002/jcc.21478.

Abstract

We present a Lamarckian genetic algorithm (LGA) variant for flexible ligand-receptor docking which allows to handle a large number of degrees of freedom. Our hybrid method combines a multi-deme LGA with a recently published gradient-based method for local optimization of molecular complexes. We compared the performance of our new hybrid method to two non gradient-based search heuristics on the Astex diverse set for flexible ligand-receptor docking. Our results show that the novel approach is clearly superior to other LGAs employing a stochastic optimization method. The new algorithm features a shorter run time and gives substantially better results, especially with increasing complexity of the ligands. Thus, it may be used to dock ligands with many rotatable bonds with high efficiency.

MeSH terms

  • Algorithms*
  • Computer Simulation
  • Ligands
  • Models, Genetic*
  • Protein Conformation
  • Proteins / chemistry*
  • Proteins / metabolism

Substances

  • Ligands
  • Proteins