| Literature DB >> 32659039 |
Hao Sun1, Wei Cao1, Nanzhi Zang1, Tristan D Clemons1,2, Georg M Scheutz3, Ziying Hu1, Matthew P Thompson1, Yifei Liang1, Maria Vratsanos1, Xuhao Zhou1, Wonmin Choi1, Brent S Sumerlin3, Samuel I Stupp1,2,4, Nathan C Gianneschi1,5,2.
Abstract
Herein, we report the photoinitiated polymerization-induced self-assembly (photo-PISA) of spherical micelles consisting of proapoptotic peptide-polymer amphiphiles. The one-pot synthetic approach yielded micellar nanoparticles at high concentrations and at scale (150 mg mL-1 ) with tunable peptide loadings up to 48 wt. %. The size of the micellar nanoparticles was tuned by varying the lengths of hydrophobic and hydrophilic building blocks. Critically, the peptide-functionalized nanoparticles imbued the proapoptotic "KLA" peptides (amino acid sequence: KLAKLAKKLAKLAK) with two key properties otherwise not inherent to the sequence: 1) proteolytic resistance compared to the oligopeptide alone; 2) significantly enhanced cell uptake by multivalent display of KLA peptide brushes. The result was demonstrated improved apoptosis efficiency in HeLa cells. These results highlight the potential of photo-PISA in the large-scale synthesis of functional, proteolytically resistant peptide-polymer conjugates for intracellular delivery.Entities:
Keywords: nanoparticles; peptide delivery; peptide-polymer conjugates; polymerization; scaled synthesis
Year: 2020 PMID: 32659039 PMCID: PMC7722202 DOI: 10.1002/anie.202006385
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336