The control of the DNA condensation process is essential for compaction of DNA in chromatin, as well as for biological applications such as nonviral gene therapy. This review endeavours to reflect the progress of investigations on DNA condensation effects of nanostructure-based condensing agents (such as nanoparticles, nanotubes, cationic polymer and peptide agents) observed by using atomic force microscopy (AFM) and other techniques. The environmental effects on structural characteristics of nanostructure-induced DNA condensates are also discussed.
Nonviral vectors are highly desirable
for the development of efficient
gene delivery systems. In this study, we report the monomolecular
condensation of plasmid DNA and efficient cell transfection by imidazolium
gemini surfactants ([C12-4-C12im]Br2), which could be a potential nonviral vector for efficient gene
therapy. Homogeneous DNA/[C12-4-C12im]Br2 nanoparticles are formed with a diameter of approximately
100 nm and investigated by using atomic force microscopy. DNA condensates
evolve from supercoiled DNA molecules, to individual toroids, to close-packed
particles, and eventually to multimolecular aggregates with the increase
of [C12-4-C12im]Br2 concentrations.
Highly efficient gene transfection in vitro is demonstrated in human
embryonic kidney 293 (HEK293) and HeLa cells, which could be attributed
to the effective DNA condensation into uniform nanoparticles induced
by [C12-4-C12im]Br2. In addition,
the low cytotoxicity of [C12-4-C12im]Br2 at transfection concentration region verified by cell viability
assay (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl tetrazolium bromide,
MTT assay) also supports [C12-4-C12im]Br2 as an effective gene vector. The high gene transfection efficiency
by [C12-4-C12im]Br2 as well as its
low cytotoxicity could shed light on the rational molecular design
of nonviral vectors for gene delivery systems.
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