Nonviral gene delivery is hampered by difficulties associated with transporting negatively charged DNA through the cell membrane and, more importantly, the nuclear envelope of target cells. Here we show for the first time that chromatin reconstituted with histone H2B proteins optimized for nuclear targeting can be used as an efficient means to deliver DNA to the nucleus of intact living mammalian cells, resulting in high levels of transgene expression that were ∼6-fold more than those achieved by commercial liposomal preparations. The high efficiency is due in part to DNA condensation and protection against degradation in the reconstituted chromatin, as well as its ability to interact with high affinity with the importin proteins of the cel...
Gene therapy, the expression in cells of genetic material that has therapeutic activity, holds great...
Gene therapy utilizes genetic material in order to cure patients either by DNA vaccines or by replac...
Inefficient nuclear delivery restricts transgene expression using polyelectrolyte DNA vectors. To in...
Gene delivery into the nucleus of eukaryotic cells is inefficient, largely because of the significan...
We describe here a unique transfer system based on a truncated form of the human linker histone H1F4...
Currently a protein/peptide-mediated gene delivery has been considered a promising approach in non-v...
We report a novel system for efficient and specific targeted delivery of large nucleic acids to and ...
Delivery of transgenic DNA into mammalian cells is critical to realizing the potential of synthetic ...
Gene therapy has the potential to treat a wide variety of inherited and acquired genetic diseases th...
Sullivan, MillicentNucleic acid delivery has garnered significant attention as an innovative therape...
For successful gene delivery, plasmid DNA must be able to access the nucleus in order to be transcri...
To improve the nuclear-targeted delivery of non-viral vectors, extensive effort has been carried out...
Nonviral gene delivery has seen limited clinical application due in part to the inefficiency with wh...
Import of exogenous plasmid DNA (pDNA) into mammalian cell nuclei represents a key intracellular obs...
An interest in nuclear proteins as possible gene vectors arose as early as 1988. Nuclear proteins po...
Gene therapy, the expression in cells of genetic material that has therapeutic activity, holds great...
Gene therapy utilizes genetic material in order to cure patients either by DNA vaccines or by replac...
Inefficient nuclear delivery restricts transgene expression using polyelectrolyte DNA vectors. To in...
Gene delivery into the nucleus of eukaryotic cells is inefficient, largely because of the significan...
We describe here a unique transfer system based on a truncated form of the human linker histone H1F4...
Currently a protein/peptide-mediated gene delivery has been considered a promising approach in non-v...
We report a novel system for efficient and specific targeted delivery of large nucleic acids to and ...
Delivery of transgenic DNA into mammalian cells is critical to realizing the potential of synthetic ...
Gene therapy has the potential to treat a wide variety of inherited and acquired genetic diseases th...
Sullivan, MillicentNucleic acid delivery has garnered significant attention as an innovative therape...
For successful gene delivery, plasmid DNA must be able to access the nucleus in order to be transcri...
To improve the nuclear-targeted delivery of non-viral vectors, extensive effort has been carried out...
Nonviral gene delivery has seen limited clinical application due in part to the inefficiency with wh...
Import of exogenous plasmid DNA (pDNA) into mammalian cell nuclei represents a key intracellular obs...
An interest in nuclear proteins as possible gene vectors arose as early as 1988. Nuclear proteins po...
Gene therapy, the expression in cells of genetic material that has therapeutic activity, holds great...
Gene therapy utilizes genetic material in order to cure patients either by DNA vaccines or by replac...
Inefficient nuclear delivery restricts transgene expression using polyelectrolyte DNA vectors. To in...