Synthesis of Short Peptides with Perfluoroalkyl Side Chains and Evaluation of Their Cellular Uptake Efficiency

Chembiochem. 2023 Nov 2;24(21):e202300374. doi: 10.1002/cbic.202300374. Epub 2023 Jul 26.

Abstract

With an increasing demand for macromolecular biotherapeutics, the issue of their poor cell-penetrating abilities requires viable and relevant solutions. Herein, we report tripeptides bearing an amino acid with a perfluoroalkyl (RF ) group adjacent to the α-carbon. RF -containing tripeptides were synthesized and evaluated for their ability to transport a conjugated hydrophilic dye (Alexa Fluor 647) into the cells. RF -containing tripeptides with the fluorophore showed high cellular uptake efficiency and none of them were cytotoxic. Interestingly, we demonstrated that the absolute configuration of perfluoroalkylated amino acids (RF -AAs) affects not only nanoparticle formation but also the cell permeability of the tripeptides. These novel RF -containing tripeptides are potentially useful as short and noncationic cell-penetrating peptides (CPPs).

Keywords: cell-penetrating peptide; drug delivery system; fluorinated amino acids; nanoparticles; perfluoroalkyl.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / metabolism
  • Antineoplastic Agents*
  • Biological Transport
  • Cell-Penetrating Peptides* / chemistry
  • Fluorocarbons*

Substances

  • Cell-Penetrating Peptides
  • Antineoplastic Agents
  • Amino Acids
  • Fluorocarbons