Certain protein transducing agents convert translocated proteins into cell killers

Acta Biochim Pol. 2012;59(3):433-9. Epub 2012 Sep 3.

Abstract

The majority of proteins are unable to translocate into the cell interior. Hence for peptide- and protein-based therapeutics a direct intracytoplasmic delivery with the aid of transducing agents is an attractive approach. We wanted to deliver to the cell interior a putatively cytotoxic protein VPg. Protein transduction was achieved in vitro with three different commercial products. However, in our hands, delivery of various control proteins without known deleterious effects, as well as of protein VPg, always induced cell death. Finally, we used a novel transducing peptide Wr-T, which was not toxic to cultured cells, even in a quite large range of concentrations. Most importantly, control protein delivered to cells in culture did not display any toxicity while VPg protein exerted a strong cytotoxic effect. These data show that results obtained with cell-penetrating agents should be interpreted with caution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology
  • Cell Death
  • Cell Proliferation
  • Cell Survival
  • Culture Media, Serum-Free
  • Drug Delivery Systems / methods
  • Drug Delivery Systems / standards
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Green Fluorescent Proteins / metabolism
  • HeLa Cells
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Microscopy, Fluorescence
  • Molecular Sequence Data
  • Peptides / metabolism
  • Peptides / pharmacology*
  • Plasmids / genetics
  • Plasmids / metabolism
  • Protein Transport*
  • Time Factors
  • Transfection
  • Viral Proteins / genetics
  • Viral Proteins / pharmacology*

Substances

  • Antineoplastic Agents
  • Culture Media, Serum-Free
  • Peptides
  • Viral Proteins
  • enhanced green fluorescent protein
  • Green Fluorescent Proteins
  • L-Lactate Dehydrogenase