The polymeric properties of DNA molecules, which are electrostatically bound to glass-supported cationic lipid membranes, are investigated. The electrostatic interaction is sufficiently strong to hold DNA flat onto the fluid lipid surface but allows DNA to diffuse freely in-plane. The molecules are fluorescently labeled, and fluorescence images are examined in terms of real-space monomer distributions of polymer chains. The chain extension of single DNA fragments of restriction enzyme digests shows power law scaling with number of base pairs in accordance with self-avoiding walks in two dimensions. Dynamic scaling is found for center-of-mass diffusion following Rouse dynamics, D ∼ 1/ N, and for rotational relaxation times, τ r ∝ N μ with μ = 2.6 ± 0.4. A crowded surface of monodisperse λ-DNA behaves like a two-dimensional semidilute solution with a measurable correlation length ξ being smaller than for dilute preparations. Polymer unbinding and the role of surface defects are discussed.
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Maier et al. (2000) studied this question.
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