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- W2895519614 abstract "Even though the persistence length ${L}_{P}$ of double-stranded DNA plays a pivotal role in cell biology and nanotechnologies, its dependence on ionic strength $I$ lacks a consensual description. Using a high-throughput single-molecule technique and statistical physics modeling, we measure ${L}_{P}$ in the presence of monovalent (${mathrm{Li}}^{+}$, ${mathrm{Na}}^{+}$, ${mathrm{K}}^{+}$) and divalent (${mathrm{Mg}}^{2+}$, ${mathrm{Ca}}^{2+}$) metallic and alkyl ammonium ions, over a large range $0.5text{ }text{ }mathrm{mM}ensuremath{le}Iensuremath{le}5text{ }text{ }mathrm{M}$. We show that linear Debye-Huckel-type theories do not describe even part of these data. By contrast, the Netz-Orland and Trizac-Shen formulas, two approximate theories including nonlinear electrostatic effects and the finite DNA radius, fit our data with divalent and monovalent ions, respectively, over the whole $I$ range. Furthermore, the metallic ion type does not influence ${L}_{P}(I)$, in contrast to alkyl ammonium monovalent ions at high $I$." @default.
- W2895519614 created "2018-10-12" @default.
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- W2895519614 date "2019-01-18" @default.
- W2895519614 modified "2023-10-18" @default.
- W2895519614 title "Dependence of DNA Persistence Length on Ionic Strength and Ion Type" @default.
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- W2895519614 doi "https://doi.org/10.1103/physrevlett.122.028102" @default.
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