Cargando…

Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery

[Image: see text] Development of safe and effective delivery vectors is a critical challenge for the application of RNA interference (RNAi)-based biotechnologies. In this study we show the rational design of a series of novel dendritic peptide bolaamphiphile vectors that demonstrate high efficiency...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeng, Hanxiang, Johnson, Mark E., Oldenhuis, Nathan J., Tiambeng, Timothy N., Guan, Zhibin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582325/
https://www.ncbi.nlm.nih.gov/pubmed/26436138
http://dx.doi.org/10.1021/acscentsci.5b00233
_version_ 1782391685861343232
author Zeng, Hanxiang
Johnson, Mark E.
Oldenhuis, Nathan J.
Tiambeng, Timothy N.
Guan, Zhibin
author_facet Zeng, Hanxiang
Johnson, Mark E.
Oldenhuis, Nathan J.
Tiambeng, Timothy N.
Guan, Zhibin
author_sort Zeng, Hanxiang
collection PubMed
description [Image: see text] Development of safe and effective delivery vectors is a critical challenge for the application of RNA interference (RNAi)-based biotechnologies. In this study we show the rational design of a series of novel dendritic peptide bolaamphiphile vectors that demonstrate high efficiency for the delivery of small interfering RNA (siRNA) while exhibiting low cytotoxicity and hemolytic activity. Systematic investigation into structure–property relationships revealed an important correlation between molecular design, self-assembled nanostructure, and biological activity. The unique bolaamphiphile architecture proved a key factor for improved complex stability and transfection efficiency. The optimal vector contains a fluorocarbon core and exhibited enhanced delivery efficiency to a variety of cell lines and improved serum resistance when compared to hydrocarbon analogues and lipofectamine RNAiMAX. In addition to introducing a promising new vector system for siRNA delivery, the structure–property relationships and “fluorocarbon effect” revealed herein offer critical insight for further development of novel materials for nucleic acid delivery and other biomaterial applications.
format Online
Article
Text
id pubmed-4582325
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-45823252015-10-01 Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery Zeng, Hanxiang Johnson, Mark E. Oldenhuis, Nathan J. Tiambeng, Timothy N. Guan, Zhibin ACS Cent Sci [Image: see text] Development of safe and effective delivery vectors is a critical challenge for the application of RNA interference (RNAi)-based biotechnologies. In this study we show the rational design of a series of novel dendritic peptide bolaamphiphile vectors that demonstrate high efficiency for the delivery of small interfering RNA (siRNA) while exhibiting low cytotoxicity and hemolytic activity. Systematic investigation into structure–property relationships revealed an important correlation between molecular design, self-assembled nanostructure, and biological activity. The unique bolaamphiphile architecture proved a key factor for improved complex stability and transfection efficiency. The optimal vector contains a fluorocarbon core and exhibited enhanced delivery efficiency to a variety of cell lines and improved serum resistance when compared to hydrocarbon analogues and lipofectamine RNAiMAX. In addition to introducing a promising new vector system for siRNA delivery, the structure–property relationships and “fluorocarbon effect” revealed herein offer critical insight for further development of novel materials for nucleic acid delivery and other biomaterial applications. American Chemical Society 2015-08-14 2015-09-23 /pmc/articles/PMC4582325/ /pubmed/26436138 http://dx.doi.org/10.1021/acscentsci.5b00233 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Zeng, Hanxiang
Johnson, Mark E.
Oldenhuis, Nathan J.
Tiambeng, Timothy N.
Guan, Zhibin
Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery
title Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery
title_full Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery
title_fullStr Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery
title_full_unstemmed Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery
title_short Structure-Based Design of Dendritic Peptide Bolaamphiphiles for siRNA Delivery
title_sort structure-based design of dendritic peptide bolaamphiphiles for sirna delivery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582325/
https://www.ncbi.nlm.nih.gov/pubmed/26436138
http://dx.doi.org/10.1021/acscentsci.5b00233
work_keys_str_mv AT zenghanxiang structurebaseddesignofdendriticpeptidebolaamphiphilesforsirnadelivery
AT johnsonmarke structurebaseddesignofdendriticpeptidebolaamphiphilesforsirnadelivery
AT oldenhuisnathanj structurebaseddesignofdendriticpeptidebolaamphiphilesforsirnadelivery
AT tiambengtimothyn structurebaseddesignofdendriticpeptidebolaamphiphilesforsirnadelivery
AT guanzhibin structurebaseddesignofdendriticpeptidebolaamphiphilesforsirnadelivery