Sm. Melnikov et al., DISCRETE COIL-GLOBULE TRANSITION OF LARGE DNA INDUCED BY CATIONIC SURFACTANT, Journal of the American Chemical Society, 117(9), 1995, pp. 2401-2408
It becomes clear that large DNA molecules exhibit discrete conformatio
nal change between the coil and globule states with the addition of a
very small amount (with the order of 10(-5) M) of cationic surfactant,
cetyltrimethylammonium bromide (CTAB). We use fluorescence microscopy
as a tool of single molecular observation of double-stranded T4DNA in
an aqueous environment. When the concentration of CTAB is less than 9
.4 x 10(-6) M, all DNA molecules exhibit the extended coil state. Wher
eas, when the CTAB concentration is higher than 2.0 x 10(-5) M, only c
ompacted DNA molecules in the globular state are observed. In the regi
on between these two critical concentrations, the coil and globule sta
tes coexist in the solution. A small but apparent increase of the size
of the DNA globule is noticed at the CTAB concentration higher than 1
0(-3) M, due to the penetration of CTAB molecules into the DNA globule
. To study the dynamical aspect of coil-globule transition, the proces
s of the structural change from the coil into the globule state is obs
erved under the spatial gradient of the CTAB concentration. The format
ion of aggregates from two or more globules is noticed at high concent
rations of surfactant above 1.6 x 10(-4) M. Below this concentration,
the globules do not coalesce into an aggregate even if they collide wi
th each other. The translational diffusion constant D of DNA molecules
is measured from the time series of video frames of the fluorescence
image. The hydrodynamic gyration radius xi(H) is evaluated from the D
and the viscosity of the bulk aqueous solutions. The increase of the g
lobule size at the higher CTAB concentrations above 10(-3) M is confir
med by the increase of xi(H) values.