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Complexation of semiflexible chains with oppositely charged cylinder

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2004
American Institute of Physics Melville, NY

The journal of chemical physics 120, 9394 - 9400 () [10.1063/1.1707015]

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Abstract: We study the complexation of long thin semiflexible polymer chains with an oppositely charged cylinder. Starting from the linear Poisson-Boltzmann equation, we calculate the electrostatic potential and the energy of such a charge distribution. We find that sufficiently flexible chains prefer to wrap around the cylinder in a helical manner, when their charge density is smaller than that of the cylinder. The optimal value of the helical pitch is found by minimization of the sum of electrostatic and bending energies. The dependence of the pitch on the number of chains, their rigidity, and salt concentration in solution is analyzed. We discuss our results in the light of recent experiments on DNA complexation with cylindrical dendronized polymers.

Keyword(s): Computer Simulation (MeSH) ; DNA: chemistry (MeSH) ; DNA: ultrastructure (MeSH) ; Models, Chemical (MeSH) ; Models, Molecular (MeSH) ; Multiprotein Complexes: chemistry (MeSH) ; Nucleic Acid Conformation (MeSH) ; Static Electricity (MeSH) ; Multiprotein Complexes ; DNA ; J


Note: Record converted from VDB: 12.11.2012

Contributing Institute(s):
  1. Theorie II (IFF-TH-II)
Research Program(s):
  1. Kondensierte Materie (M02)

Appears in the scientific report 2004
Notes: This version is available at the following Publisher URL: http://jcp.aip.org
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 Record created 2012-11-13, last modified 2024-06-10


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