Author
Listed:
- Brian C. Evans
(Vanderbilt University)
- R. Brock Fletcher
(Vanderbilt University)
- Kameron V. Kilchrist
(Vanderbilt University)
- Eric A. Dailing
(Vanderbilt University)
- Alvin J. Mukalel
(University of Pennsylvania)
- Juan M. Colazo
(Vanderbilt University
Vanderbilt University
Vanderbilt University School of Medicine)
- Matthew Oliver
(Duke University School of Medicine)
- Joyce Cheung-Flynn
(Vanderbilt University Medical Center, D-5237 Medical Center North)
- Colleen M. Brophy
(Vanderbilt University Medical Center, D-5237 Medical Center North
Veterans Affairs Medical Center, VA Tennessee Valley Healthcare System)
- John W. Tierney
(Vanderbilt University)
- Jeffrey S. Isenberg
(University of Pittsburgh)
- Kurt D. Hankenson
(University of Michigan Medical School)
- Kedar Ghimire
(University of Pittsburgh School of Medicine)
- Cynthia Lander
(Moerae Matrix Inc.)
- Charles A. Gersbach
(Duke University
Duke University
Duke University)
- Craig L. Duvall
(Vanderbilt University)
Abstract
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.
Suggested Citation
Brian C. Evans & R. Brock Fletcher & Kameron V. Kilchrist & Eric A. Dailing & Alvin J. Mukalel & Juan M. Colazo & Matthew Oliver & Joyce Cheung-Flynn & Colleen M. Brophy & John W. Tierney & Jeffrey S., 2019.
"An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles,"
Nature Communications, Nature, vol. 10(1), pages 1-19, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-12906-y
DOI: 10.1038/s41467-019-12906-y
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