Improvement in predicting drug sensitivity changes associated with protein mutations using a molecular dynamics based alchemical mutation method

Sci Rep. 2020 Feb 7;10(1):2161. doi: 10.1038/s41598-020-58877-9.

Abstract

While molecular-targeted drugs have demonstrated strong therapeutic efficacy against diverse diseases such as cancer and infection, the appearance of drug resistance associated with genetic variations in individual patients or pathogens has severely limited their clinical efficacy. Therefore, precision medicine approaches based on the personal genomic background provide promising strategies to enhance the effectiveness of molecular-targeted therapies. However, identifying drug resistance mutations in individuals by combining DNA sequencing and in vitro analyses is generally time consuming and costly. In contrast, in silico computation of protein-drug binding free energies allows for the rapid prediction of drug sensitivity changes associated with specific genetic mutations. Although conventional alchemical free energy computation methods have been used to quantify mutation-induced drug sensitivity changes in some protein targets, these methods are often adversely affected by free energy convergence. In this paper, we demonstrate significant improvements in prediction performance and free energy convergence by employing an alchemical mutation protocol, MutationFEP, which directly estimates binding free energy differences associated with protein mutations in three types of a protein and drug system. The superior performance of MutationFEP appears to be attributable to its more-moderate perturbation scheme. Therefore, this study provides a deeper level of insight into computer-assisted precision medicine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Reductase / antagonists & inhibitors
  • Aldehyde Reductase / chemistry
  • Aldehyde Reductase / genetics
  • Anaplastic Lymphoma Kinase / antagonists & inhibitors
  • Anaplastic Lymphoma Kinase / chemistry
  • Anaplastic Lymphoma Kinase / genetics
  • Drug Resistance*
  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology
  • Humans
  • Molecular Docking Simulation / methods*
  • Molecular Docking Simulation / standards
  • Mutation*
  • Neuraminidase / antagonists & inhibitors
  • Neuraminidase / chemistry
  • Neuraminidase / genetics
  • Sensitivity and Specificity

Substances

  • Enzyme Inhibitors
  • AKR1B1 protein, human
  • Aldehyde Reductase
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Neuraminidase