Zwitterionic peptide self-assembly has been used in antifouling coating of medical devices, coating gold nanoparticles, biointerfaces, and peptide probed atomic force microscopy. The sequence and number of charged amino acids in zwitterionic peptides determine their structural properties. Because amino acids that compose peptides are also found in nature, we can look for insight from nature. The surface of proteins is commonly populated by charged amino acids; they make up about 40% of human protein surfaces. The most common are lysine (E) and glutamic acid (K), which are capable of electrostatically interacting with water as well as each other. Their ionic hydration creates a strong solvation shell around them, as opposed to arginine (R) which interacts with E more than water. Based on their strong hydration and other evidence, E and K provide a resistance of non-specific binding and that may be the reason for their common occurrence on protein surfaces. There are still open questions about the interactions between these charged groups, especially regarding the seemingly small chemical difference between aspartic acid (D) and E which has vastly different occurrences on protein surfaces. In this work, we simulate different sequences of large multivalent zwitterionic peptide chains, (EK)6, E6K6 and a mixture E12 and K12. We examined the interplay between salt bridging, hydration, peptide structure, and multivalent interactions.<br/><br/><br/>

Self-assembly of zwitterionic peptides with multi-scale molecular dynamics simulations

Macromolecular Chemistry: The Second Century

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ACS Spring 2020 National Meeting & Expo

The official archive and repository for all ACS Meetings & Expositions abstracts and select posters or presentations.