Modulation of interaction of mutant TP53 and wild type BRCA1 by alkaloids: a computational approach towards targeting protein-protein interaction as a futuristic therapeutic intervention strategy for breast cancer impediment

J Biomol Struct Dyn. 2018 Oct;36(13):3376-3387. doi: 10.1080/07391102.2017.1388286. Epub 2017 Oct 23.

Abstract

Protein-protein interactions (PPI) are a new emerging class of novel therapeutic targets. In order to probe these interactions, computational tools provide a convenient and quick method towards the development of therapeutics. Keeping this in view the present study was initiated to analyse interaction of tumour suppressor protein p53 (TP53) and breast cancer associated protein (BRCA1) as promising target against breast cancer. Using computational approaches such as protein-protein docking, hot spot analyses, molecular docking and molecular dynamics simulation (MDS), stepwise analyses of the interactions of the wild type and mutant TP53 with that of wild type BRCA1 and their modulation by alkaloids were done. Protein-protein docking method was used to generate both wild type and mutant complexes of TP53-BRCA1. Subsequently, the complexes were docked using sixteen different alkaloids, fulfilling ADMET and Lipinski's rule of five criteria, and were compared with that of a well-known inhibitor of PPI, namely nutlin. The alkaloid dicentrine was found to be the best docked alkaloid among all the docked alklaloids as well as that of nutlin. Furthermore, MDS analyses of both wild type and mutant complexes with the best docked alkaloid i.e. dicentrine, revealed higher stability of mutant complex than that of the wild one, in terms of average RMSD, RMSF and binding free energy, corroborating the results of docking. Results suggested more pronounced interaction of BRCA1 with mutant TP53 leading to increased expression of mutated TP53 thus showing a dominant negative gain of function and hampering wild type TP53 function leading to tumour progression.

Keywords: TP53-BRCA1; alkaloids; breast cancer; molecular dynamics simulation; protein–protein interaction.

MeSH terms

  • Aporphines / chemistry*
  • BRCA1 Protein / chemistry*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology*
  • Female
  • Humans
  • Hydrogen Bonding
  • Imidazoles / chemistry*
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Piperazines / chemistry*
  • Protein Interaction Maps
  • Protein Structure, Secondary
  • Tumor Suppressor Protein p53 / chemistry*

Substances

  • Aporphines
  • BRCA1 Protein
  • BRCA1 protein, human
  • Imidazoles
  • Piperazines
  • TP53 protein, human
  • Tumor Suppressor Protein p53
  • nutlin 1
  • dicentrine