Hydrogen Bonding versus Ion Pairing in Polyelectrolyte Multilayers with Homopolynucleotides

• Published in: Biomacromolecules 2007-01, Vol.8 (1), p.59-64
• Main Authors: Markarian, Marie Z, Moussallem, Maroun D, Jomaa, Houssam W, Schlenoff, Joseph B
• Format: Article
• Language: English
• Subjects: Adsorption; Applied sciences; Chemical Phenomena; Chemistry, Physical; Circular Dichroism; Dose-Response Relationship, Drug; Electrolytes; Exact sciences and technology; Hydrogen Bonding; Ions; Microscopy, Atomic Force; Molecular Conformation; Nucleotides - chemistry; Organic polymers; Physicochemistry of polymers; Polyethyleneimine - chemistry; Polynucleotides - chemistry; Properties and characterization; Salts - chemistry; Structure, morphology and analysis; Surface Properties; Time Factors
• ISSN: 1525-7797; 1526-4602
• DOI: 10.1021/bm0604909

Homopolynucleotidespoly(adenylic acid), poly(A), and poly(uridylic acid), poly(U)were assembled, layer-by-layer, into thin films with poly(ethylenimine), PEI. Various combinations and sequences of polynucleotide and PEI were used to highlight contributions of electrostatic versus hydrogen bonding as driving forces for multilayer build-up. Assembly of alternating poly(A) and poly(U) failed to yield growing films, due to excessively strong interactions between these complimentary strands. The surface morphology of multilayers depended on the deposition order and whether films had been annealed by salt. Films assembled from preformed A/U duplexes (having high persistence lengths) were very smooth. Individual adsorption steps, followed by optical waveguide light-mode spectroscopy, showed that only complementary polynucleotides adsorb by H-bonding to the surface of a growing multilayer. In contrast to behavior usually observed for polyelectrolyte multilayer build-up, the films decreased in thickness with increasing salt concentration.