TY - JOUR
T1 - Sheltering DNA in self-organizing, protein-only nano-shells as artificial viruses for gene delivery
AU - Unzueta, Ugutz
AU - Saccardo, Paolo
AU - Domingo-Espín, Joan
AU - Cedano, Juan
AU - Conchillo-Solé, Oscar
AU - García-Fruitós, Elena
AU - Céspedes, María Virtudes
AU - Corchero, José Luis
AU - Daura, Xavier
AU - Mangues, Ramón
AU - Ferrer-Miralles, Neus
AU - Villaverde, Antonio
AU - Vázquez, Esther
PY - 2014/1/1
Y1 - 2014/1/1
N2 - By recruiting functional domains supporting DNA condensation, cell binding, internalization, endosomal escape and nuclear transport, modular single-chain polypeptides can be tailored to associate with cargo DNA for cell-targeted gene therapy. Recently, an emerging architectonic principle at the nanoscale has permitted tagging protein monomers for self-organization as protein-only nanoparticles. We have studied here the accommodation of plasmid DNA into protein nanoparticles assembled with the synergistic assistance of end terminal poly-arginines (R9) and poly-histidines (H6). Data indicate a virus-like organization of the complexes, in which a DNA core is surrounded by a solvent-exposed protein layer. This finding validates end-terminal cationic peptides as pleiotropic tags in protein building blocks for the mimicry of viral architecture in artificial viruses, representing a promising alternative to the conventional use of viruses and virus-like particles for nanomedicine and gene therapy. © 2014 Elsevier Inc.
AB - By recruiting functional domains supporting DNA condensation, cell binding, internalization, endosomal escape and nuclear transport, modular single-chain polypeptides can be tailored to associate with cargo DNA for cell-targeted gene therapy. Recently, an emerging architectonic principle at the nanoscale has permitted tagging protein monomers for self-organization as protein-only nanoparticles. We have studied here the accommodation of plasmid DNA into protein nanoparticles assembled with the synergistic assistance of end terminal poly-arginines (R9) and poly-histidines (H6). Data indicate a virus-like organization of the complexes, in which a DNA core is surrounded by a solvent-exposed protein layer. This finding validates end-terminal cationic peptides as pleiotropic tags in protein building blocks for the mimicry of viral architecture in artificial viruses, representing a promising alternative to the conventional use of viruses and virus-like particles for nanomedicine and gene therapy. © 2014 Elsevier Inc.
KW - Artificial viruses
KW - Gene therapy
KW - Nanoparticles
KW - Protein building blocks
KW - Self-assembling
U2 - 10.1016/j.nano.2013.11.006
DO - 10.1016/j.nano.2013.11.006
M3 - Article
SN - 1549-9634
VL - 10
SP - 535
EP - 541
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
ER -