Investigation of the elasticity of a cisplatin-DNA adduct via single-molecule measurements and bimodal modeling

Nam-Kyung Lee, Jin-Sung Park, Albert Johner, Sergei Obukhov, Ju-Yong Hyon, Kyoung J. Lee, and Seok-Cheol Hong
Phys. Rev. E 79, 041921 – Published 22 April 2009

Abstract

Cisplatin has been known as an anticancer drug for a long time. It is therapeutically active upon binding to DNA. A double-bound cisplatin bends DNA into a localized kink. We model the elastic properties of cisplatin-DNA adducts at moderate tension (<6pN). It is shown that from the mechanical point of view the action of cisplatin can be revealed by reduced persistence length. We derived two expressions for the persistence length, which apply in the linear-response and the strong-force regimes, respectively. Experimental data for DNA adducts stretched by magnetic tweezers are consistently fitted by these expressions. This allows us to estimate the degree of platination at various salt concentrations.

    • Received 15 January 2009

    DOI:https://doi.org/10.1103/PhysRevE.79.041921

    ©2009 American Physical Society

    Authors & Affiliations

    Nam-Kyung Lee1,2,*, Jin-Sung Park3, Albert Johner2, Sergei Obukhov2,4, Ju-Yong Hyon5, Kyoung J. Lee3, and Seok-Cheol Hong3,†

    • 1Department of Physics, Institute of Fundamental Physics, Sejong University, Seoul 143-743, Korea
    • 2Institut Charles Sadron, 670 83 Strasbourg Cedex, France
    • 3Department of Physics, Korea University, Seoul 136-713, Korea
    • 4Department of Physics, University of Florida, Gainesville, Florida 32611, USA
    • 5Bio-microsystems Technology Program, Korea University, Seoul 136-713, Korea

    • *lee@sejong.ac.kr
    • hongsc@korea.ac.kr

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    Issue

    Vol. 79, Iss. 4 — April 2009

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