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Biopolymer hairpin loops sustained by polarons

B. Chakrabarti*, B. M. A. G. Piette, and W. J. Zakrzewski

  • Department of Mathematical Sciences, University of Durham, Durham DH1 3LE, United Kingdom

  • *buddhapriya.chakrabarti@durham.ac.uk
  • b.m.a.g.piette@durham.ac.uk
  • w.j.zakrzewski@durham.ac.uk

Phys. Rev. E 86, 021910 – Published 9 August, 2012

DOI: https://doi.org/10.1103/PhysRevE.86.021910

Abstract

We show that polarons can sustain looplike configurations in flexible biopolymers and that the size of the loops depend on both the flexural rigidity of the polymer and the electron-phonon coupling constant. In particular we show that for single stranded DNA (ssDNA) and polyacetylene such loops can have as few as seven monomers. We also show that these configurations are very stable under thermal fluctuations and so could facilitate the formation of hairpin loops of ssDNA.

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References (20)

  1. B. Schnurr, F. C. Mackintosh, and D. R. Williams, Europhys. Lett. 51, 279 (2000).
  2. B. Schnurr, F. Gittes, and F. C. MacKintosh, Phys. Rev. E 65, 061904 (2002).
  3. S. F. Mingaleev, Y. B. Gaididei, P. L. Christiansen, and Y. S. Kivshar, Europhys. Lett. 59, 403 (2002).
  4. A. S. Davydov, J. Theor. Biol. 38, 559 (1973).
  5. A. S. Davydov, Phys. Scr. 20, 387 (1979).
  6. A. S. Davydov, Phys. D 3, 1 (1981).
  7. M. T. Woodside, W. M. Behnke-Parks, K. Larizadeh, K. Travers, D. Herschlag, and S. M. Block, Proc. Natl. Acad. Sci. USA 103, 6190 (2006).
  8. A. N. Gupta, A. Vincent, K. Neupane, H. Yu, F. Wang, and M. T. Woodside, Nat. Phys. 7, 631 (2011).
  9. B. Chakrabarti, B. M. A. G. Piette, and W. J. Zakrzewski, Europhys. Lett. 97, 4705 (2012).
  10. R. M. Wadkins, Curr. Med. Chem. 7, 1 (2000) [http://www.ingentaconnect.com/content/ben/cmc/2000/00000007/00000001/art00002].
  11. A. M. Gacy, G. Goellner, N. Juranic, S. Macura, and C. T. McMurray, Cell 81, 533 (1995).
  12. M. A. Glucksmann-Kuis, X. Dai, P. Markiewicz, and L. B Rothman-Denes, Cell 84, 147 (1996).
  13. M. Mandelkern, J. Elias, D. Eden, and D. Crothers, J. Mol. Biol. 152, 153 (1981).
  14. S. B. Smith, Y. Cui, and C. Bustamante, Science 271, 795 (1996).
  15. G. Bonnet, O. Krichevsky, and A. Libchaber, Proc. Natl. Acad. Sci. USA 95, 8602 (1998).
  16. M. Kenward and K. D. Dorfman, J. Chem. Phys. 130, 095101 (2009).
  17. S. M. Kravec, C. D. Kinz-Thompson, and E. M. Conwell, J. Phys. Chem. B 115, 6166 (2011).
  18. A. K. Thazhathveetil, A. Trifonov, M. R. Wasielewski, and F. D. Lewis, J. Am. Chem. Soc. 133, 11485 (2011).
  19. A. J. Heeger, S. Kivelson, J. R. Schrieffer, and W.-P. Su, Rev. Mod. Phys. 60, 781 (1988).
  20. F. L. VanNice, F. S. Bates, G. L. Baker, P. J. Carroll, and G. D. Patterson, Macromolecules 17, 2626 (1984).

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