Büyükdağlı, ŞahinPodgornik, R.2020-02-112020-02-1120192470-0045http://hdl.handle.net/11693/53255We characterize the role of charge correlations in the adsorption of a short, rodlike anionic polyelectrolyte onto a similarly charged membrane. Our theory reveals two different mechanisms driving the like-charge polyelectrolyte-membrane complexation: In weakly charged membranes, repulsive polyelectrolyte-membrane interactions lead to the interfacial depletion and a parallel orientation of the polyelectrolyte with respect to the membrane; while in the intermediate membrane charge regime, the interfacial counterion excess gives rise to an attractive “salt-induced” image force. This furthermore results in an orientational transition from a parallel to a perpendicular configuration and a subsequent short-ranged like-charge adsorption of the polyelectrolyte to the substrate. A further increase of the membrane charge engenders a charge inversion, originating from surface-induced ionic correlations, that act as a separate mechanism capable of triggering the like-charge polyelectrolyte-membrane complexation over an extended distance interval from the membrane surface. The emerging picture of this complexation phenomenon identifies the interfacial “salt-induced” image forces as a powerful control mechanism in polyelectrolyte-membrane complexation.EnglishAdsorptionBiomolecular interactionsDepletion interactionsElectric field effectsElectrostatic interactionsPolymer conformation changesThermodynamicsOrientational transition and complexation of DNA with anionic membranes: weak and intermediate electrostatic couplingArticle10.1103/PhysRevE.99.062501