Elasticity of Cisplatin-Bound DNA Reveals the Degree of Cisplatin Binding

Nam-Kyung Lee, Jin-Sung Park, Albert Johner, Sergei Obukhov, Ju-Yong Hyon, Kyoung J. Lee, and Seok-Cheol Hong
Phys. Rev. Lett. 101, 248101 – Published 9 December 2008

Abstract

Cisplatin was incidentally discovered to suppress cell division and became one of the most successful antitumor drugs. It is therapeutically active upon binding to DNA and locally kinking it. We demonstrate that after a bimodal modeling, the degree of platination of a single DNA molecule can be consistently and reliably estimated from elasticity measurements performed with magnetic tweezers. We predicted and measured for the first time two separate persistence lengths of kinked DNA at high and low tensions. We also directly observed that the degree of platination of DNA strongly depends on the concentration of sodium chloride as required for cisplatin’s intracellular activity. Our study shows that micromanipulation techniques accurately reveal the degree of chemical modification of DNA which can be used for a new type of structure-sensitive biosensors.

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  • Received 22 March 2008

DOI:https://doi.org/10.1103/PhysRevLett.101.248101

©2008 American Physical Society

Authors & Affiliations

Nam-Kyung Lee1,2, Jin-Sung Park3, Albert Johner2, Sergei Obukhov4,2, Ju-Yong Hyon5, Kyoung J. Lee3, and Seok-Cheol Hong3,*

  • 1Institute of Fundamental Physics, Department of Physics, Sejong University, Seoul 143-743, Korea
  • 2Institut Charles Sadron, 67083 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

  • *Corresponding author. hongsc@korea.ac.kr

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Issue

Vol. 101, Iss. 24 — 12 December 2008

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