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An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles.

Publication ,  Journal Article
Evans, BC; Fletcher, RB; Kilchrist, KV; Dailing, EA; Mukalel, AJ; Colazo, JM; Oliver, M; Cheung-Flynn, J; Brophy, CM; Tierney, JW; Isenberg, JS ...
Published in: Nature communications
November 2019

Peptides and biologics provide unique opportunities to modulate intracellular targets not druggable by conventional small molecules. Most peptides and biologics are fused with cationic uptake moieties or formulated into nanoparticles to facilitate delivery, but these systems typically lack potency due to low uptake and/or entrapment and degradation in endolysosomal compartments. Because most delivery reagents comprise cationic lipids or polymers, there is a lack of reagents specifically optimized to deliver cationic cargo. Herein, we demonstrate the utility of the cytocompatible polymer poly(propylacrylic acid) (PPAA) to potentiate intracellular delivery of cationic biomacromolecules and nano-formulations. This approach demonstrates superior efficacy over all marketed peptide delivery reagents and enhances delivery of nucleic acids and gene editing ribonucleoproteins (RNPs) formulated with both commercially-available and our own custom-synthesized cationic polymer delivery reagents. These results demonstrate the broad potential of PPAA to serve as a platform reagent for the intracellular delivery of cationic cargo.

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Published In

Nature communications

DOI

EISSN

2041-1723

ISSN

2041-1723

Publication Date

November 2019

Volume

10

Issue

1

Start / End Page

5012

Related Subject Headings

  • Reproducibility of Results
  • Rats
  • RAW 264.7 Cells
  • Polymers
  • Peptides
  • Nanoparticles
  • NIH 3T3 Cells
  • Mice
  • Macromolecular Substances
  • MCF-7 Cells
 

Citation

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Evans, B. C., Fletcher, R. B., Kilchrist, K. V., Dailing, E. A., Mukalel, A. J., Colazo, J. M., … Duvall, C. L. (2019). An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles. Nature Communications, 10(1), 5012. https://doi.org/10.1038/s41467-019-12906-y
Evans, Brian C., R Brock Fletcher, Kameron V. Kilchrist, Eric A. Dailing, Alvin J. Mukalel, Juan M. Colazo, Matthew Oliver, et al. “An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles.Nature Communications 10, no. 1 (November 2019): 5012. https://doi.org/10.1038/s41467-019-12906-y.
Evans BC, Fletcher RB, Kilchrist KV, Dailing EA, Mukalel AJ, Colazo JM, et al. An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles. Nature communications. 2019 Nov;10(1):5012.
Evans, Brian C., et al. “An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles.Nature Communications, vol. 10, no. 1, Nov. 2019, p. 5012. Epmc, doi:10.1038/s41467-019-12906-y.
Evans BC, Fletcher RB, Kilchrist KV, Dailing EA, Mukalel AJ, Colazo JM, Oliver M, Cheung-Flynn J, Brophy CM, Tierney JW, Isenberg JS, Hankenson KD, Ghimire K, Lander C, Gersbach CA, Duvall CL. An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles. Nature communications. 2019 Nov;10(1):5012.

Published In

Nature communications

DOI

EISSN

2041-1723

ISSN

2041-1723

Publication Date

November 2019

Volume

10

Issue

1

Start / End Page

5012

Related Subject Headings

  • Reproducibility of Results
  • Rats
  • RAW 264.7 Cells
  • Polymers
  • Peptides
  • Nanoparticles
  • NIH 3T3 Cells
  • Mice
  • Macromolecular Substances
  • MCF-7 Cells