Va. Kabanov et al., INTERACTION OF POLYIONS WITH CELL-MIMETIC SPECIES - PHYSICOCHEMICAL AND BIOMEDICAL ASPECTS, Journal of controlled release, 39(2-3), 1996, pp. 173-189
The possibility of recognition and discrimination of relatively large
charged supermolecular objects (latex species) by an oppositely charge
d polyion is demonstrated using a suspension of carboxylated and prote
in-modified latex particles interacting with the high molecular mass l
inear polycations including those conjugated with the specific protein
(alpha-chymotrypsin). The polycations are strongly adsorbed on the la
tex surface. Nevertheless, they are able to migrate between the latex
species via occasional interparticle contacts. Finally, the interchang
ing polycations carrying the specific protein are fixed on those latex
particles which carry the complementary protein receptor (trypsin inh
ibitor from soybean). The presence of other proteins does not hinder s
uch interaction, The resulting effect is considered to mimic a physico
-chemical aspect of recognition of target cells by macromolecules comb
ined with relatively small molecular vector. Interaction of the target
cell membrane with a polycation was simulated using negatively charge
d liposomes. It was found that polycations adsorbed on the surface of
liquid liposomes can cause a significant charge asymmetry in the lipid
bilayer due to transmembrane migration of negatively charged lipids f
rom the inner to outer leaflet, At the same time the liposomal membran
e integrity can be retained and adsorbed polycations can be replaced f
rom the membrane by recomplexation with polyanion species. The establi
shed phenomena may be important for understanding the biological effec
ts of polycations. Negatively charged liquid liposomes were also used
to mimic interaction of cells with DNA-polycation and DNA-cationic sur
factant complexes used to enhance plasmid DNA translocation. It was fo
und that the complex of DNA with the polycation carrying hydrophobic s
ide groups interacted with the liposomes without dissociation and adso
rbed on the liposome surface as a whole.