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Biophys J, September 2000, p. 1447-1454, Vol. 79, No. 3
Department of Physiological Chemistry, University of Groningen, Faculty of Medical Sciences, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands
Cellular transfection can be accomplished by the use of
synthetic amphiphiles as gene carrier system. To understand the
mechanism and hence to improve the efficiency of transfection, insight
into the assembly and properties of the amphiphile/gene complex is crucial. Here, we have studied the interaction between a plasmid and
cationic amphiphiles, using a monolayer technique, and have examined
complex assembly by atomic force microscopy. The data reveal a
three-step mechanism for complex formation. In a first step, the
plasmids, interacting with the monolayer, display a strong tendency of
orientational ordering. Subsequently, individual plasmids enwrap
themselves with amphiphile molecules in a multilamellar fashion. The
size of the complex formed is determined by the supercoiled size of the
plasmid, and calculations reveal that the plasmid can be surrounded by
3 to 5 bilayers of the amphiphile. The eventual size of the
transfecting complex is finally governed by fusion events between
individually wrapped amphiphile/DNA complexes. In bulk phase, where
complex assembly is triggered by mixing amphiphilic vesicles and
plasmids, a similar wrapping process is observed. However, in this
case, imperfections in this process may give rise to a partial exposure
of plasmids, i.e., part of the plasmid is not covered with a layer of
amphiphile. We suggest that these exposed sites may act as nucleation
sites for massive lipoplex clustering, which in turn may affect
transfection efficiency.
Biophys J, September 2000, p. 1447-1454, Vol. 79, No. 3
© 2000 by the Biophysical Society 0006-3495/00/09/1447/08 $2.00
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