We report fluorescence microscopy studies of the electrophoresis of individ
ual DNA molecules electrostatically adsorbed to a cationic supported lipid
bilayer. Obstacles to uniform electrophoretic flow cause the 2-D chains to
adopt hooked conformations similar to those previously observed in 3-D elec
trophoresis experiments. Analysis of the stretch-contraction dynamics allow
s for an estimate of the obstacle density in the bilayer. Increasing the el
ectric field causes the DNA molecules to become more highly stretched and i
ncreases the electrophoretic mobility substantially. A comparison of the Ro
use relaxation time of the polymers and the average time between chain-obst
acle collisions reveals that a single-obstacle model is insufficient to des
cribe the observed dynamics but the obstacles are not dense enough to use a
reptative model. Analysis of the unhooking dynamics reveals an 80% increas
e in hydrodynamic drag as compared to free chains. Finally, we observe anom
alous diffusion of the DNA chains, with a large increase in the diffusion c
oefficient after the repeated application of high electric fields. Implicat
ions of the flow obstacles in the engineering of separation applications ar
e discussed.