Peptide-Au Clusters Induced Tumor Cells Apoptosis via Targeting Glutathione Peroxidase-1: The Molecular Dynamics Assisted Experimental Studies

Sci Rep. 2017 Mar 9;7(1):131. doi: 10.1038/s41598-017-00278-6.

Abstract

The original motivation of the article is to give a systematic investigation on the protocol of combining computer simulation and accurate synthesis of serial peptide protected gold clusters for potent tumor targeting therapy. Glutathione peroxidase-1 (GPx-1) is a crucial antioxidant selenoenzyme that regulates cellular redox level, thus becomes a potential target in cancer treatment. We firstly utilize molecular dynamic (MD) simulation to rationally design and screen serial peptide-Au cluster compounds with special peptide sequences and precise gold atoms, which can recognize and bind specific domain of GPx-1 with high affinity. The theoretical simulations were further verified by the following peptide-Au clusters synthesis and GPx-1 activity suppression studies in buffer and cells, respectively. Further cytological experiments corroborated that peptide-Au clusters are promising nanoparticles inducing tumor cells apoptosis by suppressing GPx-1 activity and increasing higher cellular reactive oxygen species level to initiate tumor cell apoptosis through intrinsic mitochondrial pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / metabolism*
  • Adenocarcinoma / therapy
  • Amino Acid Sequence
  • Apoptosis*
  • Cell Line, Tumor
  • Glutathione Peroxidase / metabolism*
  • Glutathione Peroxidase GPX1
  • Humans
  • Molecular Dynamics Simulation
  • Nanoparticles / administration & dosage
  • Nanoparticles / chemistry*
  • Peptides / chemistry
  • Peptides / pharmacokinetics
  • Reactive Oxygen Species / metabolism

Substances

  • Peptides
  • Reactive Oxygen Species
  • Glutathione Peroxidase
  • Glutathione Peroxidase GPX1
  • GPX1 protein, human