A HA2-Fusion tag limits the endosomal release of its protein cargo despite causing endosomal lysis. Academic Article uri icon

abstract

  • BACKGROUND: Protein transduction domains (PTDs) can be fused to a protein to render it cell-permeable. The delivery efficiencies of PTDs are, however, often poor because PTD-protein conjugates cannot escape from endosomes. A potential solution to this problem consists in adding HA2 analogs to the PTD-protein construct as these peptides can cause endosomal lysis upon acidification of the endosomal lumen. To date, however, the utility of HA2-based PTDs has not been clearly established. METHODS: We investigate the biophysical and cellular properties of the glutamate-rich HA2 analog E5 fused to the model protein TAT-mCherry. RESULTS: E5-TAT-mCherry causes the release of fluorescent dextrans trapped with the protein inside endosomes. Yet, E5-TAT-mCherry itself is not released in the cytosol of cells, indicating that the protein remained trapped inside endosomes even after endosomal lysis takes place. Cytosolic delivery of the protein could be achieved, however, by insertion of a disulfide bond between E5 and its cargo. CONCLUSIONS: These results show that E5 causes the retention of its fused protein inside endosomes even after lysis takes place. GENERAL SIGNIFICANCE: These data establish that HA2 analogs might not be useful PTDs unless cleavable linkers are engineered between PTD and protein cargo.

published proceedings

  • Biochim Biophys Acta

altmetric score

  • 3

author list (cited authors)

  • Lee, Y., Johnson, G., Peltier, G. C., & Pellois, J.

citation count

  • 30

complete list of authors

  • Lee, Ya-Jung||Johnson, Gregory||Peltier, Grantham C||Pellois, Jean-Philippe

publication date

  • August 2011