We describe here a unique transfer system based on a truncated form of the human linker histone H1F4 for the delivery of nucleic acids to a variety of cells. The efficiency of truncated histone H1.4F was assessed using both primary mammalian and immortalised insect and mammalian cell lines. Our results indicated that recombinant histone H1.4F was able to deliver DNA, dsRNA and siRNA in all cells tested. Quantitative analysis based on reporter gene expression or silencing of target genes revealed that the transfection efficiency of histone H1.4F was comparable to, or better than, liposome-based systems. Notably, the efficiency of histone H1.4F was associated with very low toxicity for transfected cells. The human H1.4F recombinant protein is...
Our understanding of the link between gene function and disease is constantly strengthening however ...
Gene expression studies and gene therapy require efficient gene delivery into cells. Different techn...
We report a novel system for efficient and specific targeted delivery of large nucleic acids to and ...
Currently a protein/peptide-mediated gene delivery has been considered a promising approach in non-v...
Nonviral gene delivery is hampered by difficulties associated with transporting negatively charged D...
Gene delivery into the nucleus of eukaryotic cells is inefficient, largely because of the significan...
The effective delivery of exogenous genes into eukaryotic cells is important for fundamental and bio...
Synthetic vectors based on reducible polycations consisting of histidine and polylysine residues (HI...
Nanoparticles made of plasmid DNA (pDNA) and cationic polymers are promising strategies for non-vira...
International audienceNucleic acid transfer in mammalian cels is drastically improved with devices w...
Histidine containing reducible polycations based on CH(6)K(3)H(6)C monomers (His6 RPCs), are highly ...
Developing an efficient and safe system for gene delivery is considered the bottleneck of gene thera...
Gene therapy has the potential to treat a wide variety of inherited and acquired genetic diseases th...
Nonviral gene delivery has seen limited clinical application due in part to the inefficiency with wh...
Human Artificial Chromosomes (HACs) have been confirmed as viable gene expression vectors and a pote...
Our understanding of the link between gene function and disease is constantly strengthening however ...
Gene expression studies and gene therapy require efficient gene delivery into cells. Different techn...
We report a novel system for efficient and specific targeted delivery of large nucleic acids to and ...
Currently a protein/peptide-mediated gene delivery has been considered a promising approach in non-v...
Nonviral gene delivery is hampered by difficulties associated with transporting negatively charged D...
Gene delivery into the nucleus of eukaryotic cells is inefficient, largely because of the significan...
The effective delivery of exogenous genes into eukaryotic cells is important for fundamental and bio...
Synthetic vectors based on reducible polycations consisting of histidine and polylysine residues (HI...
Nanoparticles made of plasmid DNA (pDNA) and cationic polymers are promising strategies for non-vira...
International audienceNucleic acid transfer in mammalian cels is drastically improved with devices w...
Histidine containing reducible polycations based on CH(6)K(3)H(6)C monomers (His6 RPCs), are highly ...
Developing an efficient and safe system for gene delivery is considered the bottleneck of gene thera...
Gene therapy has the potential to treat a wide variety of inherited and acquired genetic diseases th...
Nonviral gene delivery has seen limited clinical application due in part to the inefficiency with wh...
Human Artificial Chromosomes (HACs) have been confirmed as viable gene expression vectors and a pote...
Our understanding of the link between gene function and disease is constantly strengthening however ...
Gene expression studies and gene therapy require efficient gene delivery into cells. Different techn...
We report a novel system for efficient and specific targeted delivery of large nucleic acids to and ...