The issue of the nucleation and slow closure mechanisms of non superhelical
stress-induced denaturation bubbles in DNA is tackled using coarse-grained
MetaDynamics and Brownian simulations. A minimal mesoscopic model is used where
the double helix is made of two interacting bead-spring rotating strands with a
prescribed torsional modulus in the duplex state. We demonstrate that
timescales for the nucleation (resp. closure) of an approximately 10 base-pair
bubble, in agreement with experiments, are associated with the crossing of a
free-energy barrier of 22kBT (resp. 13kBT) at room
temperature T. MetaDynamics allows us to reconstruct accurately the
free-energy landscape, to show that the free-energy barriers come from the
difference in torsional energy between the bubble and duplex states, and thus
to highlight the limiting step, a collective twisting, that controls the
nucleation/closure mechanism, and to access opening time scales on the
millisecond range. Contrary to small breathing bubbles, these more than
4~base-pair bubbles are of biological relevance, for example when a preexisting
state of denaturation is required by specific DNA-binding proteins.Comment: 11 pages (5 pages and Appendix), 13 figures, published in Journal of
Chemical Physic