Revisit complexation between DNA and polyethylenimine — Effect of length of free polycationic chains on gene transfection
Publication: Research - peer-review › Journal article – Annual report year: 2010
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Revisit complexation between DNA and polyethylenimine — Effect of length of free polycationic chains on gene transfection. / Yue, Yanan; Jin, Fan; Deng, Rui; Cai, Jinge; Dai, Zhuojun; Lin, Marie C.M.; Kung, Hsiang-Fu; Mattebjerg, Maria Ahlm; Andresen, Thomas Lars; Wu, Chi.
In: Journal of Controlled Release, Vol. 152, No. 1, 2011, p. 143-151.Publication: Research - peer-review › Journal article – Annual report year: 2010
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TY - JOUR
T1 - Revisit complexation between DNA and polyethylenimine — Effect of length of free polycationic chains on gene transfection
A1 - Yue,Yanan
A1 - Jin,Fan
A1 - Deng,Rui
A1 - Cai,Jinge
A1 - Dai,Zhuojun
A1 - Lin,Marie C.M.
A1 - Kung,Hsiang-Fu
A1 - Mattebjerg,Maria Ahlm
A1 - Andresen,Thomas Lars
A1 - Wu,Chi
AU - Yue,Yanan
AU - Jin,Fan
AU - Deng,Rui
AU - Cai,Jinge
AU - Dai,Zhuojun
AU - Lin,Marie C.M.
AU - Kung,Hsiang-Fu
AU - Mattebjerg,Maria Ahlm
AU - Andresen,Thomas Lars
AU - Wu,Chi
PB - Elsevier BV
PY - 2011
Y1 - 2011
N2 - Our revisit of the complexation between DNA and polyethylenimine (PEI) by using a combination of laser light scattering and gel electrophoresis confirms that nearly all the DNA chains are complexed with PEI to form polyplexes when the molar ratio of nitrogen from PEI to phosphate from DNA (N:P) reaches ~3, irrespective of the PEI chain length and solvent. Each solution mixture with N:P>3 contains two kinds of PEI chains: bound to DNA and free in the solution. It has been shown that it is those free PEI chains that play a vital role in promoting the gene transfection. The effects of the length of the bound and free chains on the gene transfection were respectively studied. Both short and long PEI chains are capable of condensing DNA completely at N:P~3 but long ones are ~102-fold more effective in the gene transfection, apparently due to their fast endocytosis and intracellular trafficking. The cellular uptake kinetics studied by flow cytometry reveals that long free chains increase the uptake rate constant of the DNA/PEI complexes. In the intracellular pathway, they are able to prevent the development of the later endolysosomes, and facilitate the subsequent release of the polyplexes from the endosomes. Our result shows that the “proton sponge” effect is not dominant because the shut-down of the proton pump only partially attenuates the transfection efficiency. A possible mechanism is speculated and presented.
AB - Our revisit of the complexation between DNA and polyethylenimine (PEI) by using a combination of laser light scattering and gel electrophoresis confirms that nearly all the DNA chains are complexed with PEI to form polyplexes when the molar ratio of nitrogen from PEI to phosphate from DNA (N:P) reaches ~3, irrespective of the PEI chain length and solvent. Each solution mixture with N:P>3 contains two kinds of PEI chains: bound to DNA and free in the solution. It has been shown that it is those free PEI chains that play a vital role in promoting the gene transfection. The effects of the length of the bound and free chains on the gene transfection were respectively studied. Both short and long PEI chains are capable of condensing DNA completely at N:P~3 but long ones are ~102-fold more effective in the gene transfection, apparently due to their fast endocytosis and intracellular trafficking. The cellular uptake kinetics studied by flow cytometry reveals that long free chains increase the uptake rate constant of the DNA/PEI complexes. In the intracellular pathway, they are able to prevent the development of the later endolysosomes, and facilitate the subsequent release of the polyplexes from the endosomes. Our result shows that the “proton sponge” effect is not dominant because the shut-down of the proton pump only partially attenuates the transfection efficiency. A possible mechanism is speculated and presented.
U2 - 10.1016/j.jconrel.2011.03.020
DO - 10.1016/j.jconrel.2011.03.020
JO - Journal of Controlled Release
JF - Journal of Controlled Release
SN - 0168-3659
IS - 1
VL - 152
SP - 143
EP - 151
ER -