Dependence of DNA persistence length on ionic strength of solutions with monovalent and divalent salts: a joint theory-experiment study
arXiv:1504.02666 · doi:10.1016/j.bpj.2015.11.2175
Abstract
Using high-throughput Tethered Particle Motion single molecule experiments, the double-stranded DNA persistence length, , is measured in solutions with Na and Mg ions of various ionic strengths, . Several theoretical equations for are fitted to the experimental data, but no decisive theory is found which fits all the values for the two ion valencies. Properly extracted from the particle trajectory using simulations, varies from 30~nm to 55~nm, and is compared to previous experimental results. For the Na only case, is an increasing concave function of , well fitted by Manning's electrostatic stretching approach, but not by classical Odjik-Skolnick-Fixman theories with or without counter-ion condensation. With added Mg ions, shows a marked decrease at low , interpreted as an ion-ion correlation effect, with an almost linear law in , fitted by a proposed variational approach.
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