• Medientyp: E-Artikel
  • Titel: Strong and weak adsorptions of polyelectrolyte chains onto oppositely charged spheres
  • Beteiligte: Cherstvy, A. G. [Verfasser:in]; Winkler, R. G. [Verfasser:in]
  • Erschienen: American Institute of Physics, 2006
  • Erschienen in: The journal of chemical physics 125, 064904 (2006). doi:10.1063/1.2229205
  • Sprache: Englisch
  • DOI: https://doi.org/10.1063/1.2229205
  • ISSN: 0021-9606
  • Schlagwörter: Surface Properties ; Biophysics: methods ; Micelles ; Statistical ; Nucleosomes ; Electrolytes: chemistry ; Molecular Conformation ; Models ; DNA: chemistry ; Chemistry ; Adsorption ; Electrolytes ; Electrochemistry ; Static Electricity ; DNA ; Solutions ; Theoretical ; Nucleosomes: chemistry ; Physical: methods
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  • Beschreibung: We investigate the complexation of long thin polyelectrolyte (PE) chains with oppositely charged spheres. In the limit of strong adsorption, when strongly charged PE chains adapt a definite wrapped conformation on the sphere surface, we analytically solve the linear Poisson-Boltzmann equation and calculate the electrostatic potential and the energy of the complex. We discuss some biological applications of the obtained results. For weak adsorption, when a flexible weakly charged PE chain is localized next to the sphere in solution, we solve the Edwards equation for PE conformations in the Hulthen potential, which is used as an approximation for the screened Debye-Huckel potential of the sphere. We predict the critical conditions for PE adsorption. We find that the critical sphere charge density exhibits a distinctively different dependence on the Debye screening length than for PE adsorption onto a flat surface. We compare our findings with experimental measurements on complexation of various PEs with oppositely charged colloidal particles. We also present some numerical results of the coupled Poisson-Boltzmann and self-consistent field equation for PE adsorption in an assembly of oppositely charged spheres.
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