Effect of Water on the Mechanical Properties of Cyclic Peptide Polymers

Biomaterials are an important source of inspiration for the development of strong and tough materials. Many improved and optimized synthetic materials have been recently developed utilizing this bioinspiration concept. Using side-chain to-side-chain polymerization of cyclic beta-peptide rings, a novel class of nanomaterials was recently introduced with outstanding mechanical properties such as toughness values greater than natural silks. In this work, molecular dynamics is used to understand the mechanics of side-chain-to-side-chain polymerization of cyclic beta-peptide rings. Unbiased steered molecular dynamics simulations are used to show the difference in the strength of polymerized and unpolymerized processing of similar cyclic rings. The simulations are performed both in aqueous and vacuum environments to capture the role of water on the mechanical properties of the cyclic peptides. Our results show that unpolymerized peptides behave like brittle material, whereas polymerized ones can withstand some stress after initial failure with large values of strain-to-failure. Finally, we have shown that the strength of cyclic peptides in water is higher than in a vacuum.

Automated summary

Biomaterials serve as an important inspiration for the development of strong and tough materials. A novel class of nanomaterials, synthesized through side-chain to-side-chain polymerization of cyclic beta-peptide rings, exhibits outstanding mechanical properties. Molecular dynamics simulations reveal that polymerized peptides can withstand stress and have high strain-to-failure values, compared to brittle behavior of unpolymerized peptides. Additionally, the strength of cyclic peptides is higher in water than in a vacuum.