Proteoid biodynamers for safe mRNA transfection via pH-responsive nanorods enabling endosomal escape.
Biopolymer
Gene delivery
Nanorod
Polymeric vector
Stimuli-responsive
Structure analysis
mRNA delivery
Journal
Journal of controlled release : official journal of the Controlled Release Society
ISSN: 1873-4995
Titre abrégé: J Control Release
Pays: Netherlands
ID NLM: 8607908
Informations de publication
Date de publication:
01 2023
01 2023
Historique:
received:
11
07
2022
revised:
05
12
2022
accepted:
08
12
2022
pubmed:
16
12
2022
medline:
3
2
2023
entrez:
15
12
2022
Statut:
ppublish
Résumé
The recent success of mRNA vaccines using lipid-based vectors highlights the importance of strategies for nucleotide delivery under the pandemic situation. Although current mRNA delivery is focused on lipid-based vectors, still they need to be optimized for increasing stability, targeting, and efficiency, and for reducing toxicity. In this regard, other vector systems featuring smart strategies such as pH-responsive degradability and endosomal escape ability hold the potential to overcome the current limitations. Here, we report pH-responsive polymeric nanorods made of amino acid-derivatives connected by dynamic covalent bonds called proteoid-biodynamers, as mRNA vectors. They show excellent biocompatibility due to the biodegradation, and outstanding transfection. The biodynamers of Lys, His, and Arg or monomer mixtures thereof were shown to form nanocomplexes with mRNA. They outperformed conventional transfection agents three times regarding transfection efficacy in three human cell lines, with 82-98% transfection in living cells. Also, we confirmed that the biodynamers disrupted the endosomes up to 10-fold more in number than the conventional vectors. We discuss here their outstanding performance with a thorough analysis of their nanorod structure changes in endosomal microenvironments.
Identifiants
pubmed: 36521693
pii: S0168-3659(22)00833-1
doi: 10.1016/j.jconrel.2022.12.018
pii:
doi:
Substances chimiques
RNA, Messenger
0
Lipids
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
915-929Informations de copyright
Copyright © 2022 Elsevier B.V. All rights reserved.