Linear aliphatic dialkynes as alternative linkers for double-click stapling of p53-derived peptides

Chembiochem. 2014 Dec 15;15(18):2680-3. doi: 10.1002/cbic.201402374. Epub 2014 Oct 29.

Abstract

We investigated linear aliphatic dialkynes as a new structural class of i,i+7 linkers for the double-click stapling of p53-based peptides. The optimal combination of azido amino acids and dialkynyl linker length for MDM2 binding was determined. In a direct comparison between aliphatic and aromatic staple scaffolds, the aliphatic staples resulted in superior binding to MDM2 in vitro and superior p53-activating capability in cells when using a diazidopeptide derived from phage display. This work demonstrates that the nature of the staple scaffold is an important factor that can affect peptide bioactivity in cells.

Keywords: anticancer agents; click chemistry; macrocycles; peptides; stapling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkynes / chemistry*
  • Alkynes / pharmacology
  • Amino Acid Sequence
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / pharmacology
  • Azides / chemistry
  • Azides / pharmacology
  • Cell Line
  • Click Chemistry
  • Humans
  • Models, Molecular
  • Molecular Sequence Data
  • Peptides / chemistry*
  • Peptides / pharmacology
  • Proto-Oncogene Proteins c-mdm2 / antagonists & inhibitors
  • Proto-Oncogene Proteins c-mdm2 / metabolism
  • Tumor Suppressor Protein p53 / agonists
  • Tumor Suppressor Protein p53 / chemistry*
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Alkynes
  • Antineoplastic Agents
  • Azides
  • Peptides
  • Tumor Suppressor Protein p53
  • Proto-Oncogene Proteins c-mdm2