This study for the first time demonstrates phenomenon of recognition of DNA
tertiary structure by the synthetic polycationic molecules. Effects of DNA
topology were evaluated using supercoiled and linearized forms of plasmid
DNA (scDNA and lDNA). Recognition is achieved by using relatively simple ch
emical structures interacting with the DNA. Two polycations modified with w
ater-soluble poly(ethylene glycol) (PEG) chains, PEG- block-poly(N-methyl-4
-vinylpyridinium sulfate) (PEC-b-PVP) and PEG -graft-polyethyleneimine (PEG
-g-PEI) were used. When added to the mixtures of lDNA and scDNA, PEO-b-PVP
selectively bound to scDNA, while lDNA remained free. In contrast, PEO-g-PE
I interacted with both forms of the DNA present in the mixture. Distinct be
havior of two copolymers was attributed to the differences in their structu
re, particularly, charge density of the polycation blocks. Relatively small
variation in the polycation ionization state can result in drastic changes
in its behavior upon interaction with DNA. Particularly, the change of pH
from 7.0 to 5.0, increasing the charge density of PEI block in PEO-g-PEI, w
as also accompanied by the appearance of recognition phenomena. These findi
ngs uncover possibilities for the control of the processes of DNA incorpora
tion in the complexes with cationic species by altering the DNA topology, w
hich may have practical significance in using these complexes for gene deli
very.