Computational design of functional random heteropolymers through atomistic simulations
Tianyi Jin, Collin S. Lung, Ting Xu, Connor W. Coley, Alfredo Alexander-Katz
TL;DR
This paper uses simulations to understand how the chemical design of random heteropolymers affects their structure and hydration, offering insights for creating protein-like synthetic materials.
Contribution
The study provides new molecular design principles for tuning the assembly and dynamics of random heteropolymers through compositional and chemical control.
Findings
Methacrylate-based RHPs transition from rod-like to compact globules as chain length increases.
Hydration of positively charged monomers follows the Hofmeister series.
PEG side-chain length significantly affects solubility and hydration behavior.
Abstract
Random heteropolymers (RHPs) are emerging single-chain nanoparticles with great potential in protein mimicry, yet a systematic understanding of how chemical composition and monomer structures govern their structure, dynamics, and hydration remains limited. Using atomistic molecular dynamics simulations, we examine how various design parameters, including chain length, backbone architecture, charged monomer concentration, chain-level composition, and side-chain micropolarity influence RHP assembly and hydration behavior. As chain length increases, methacrylate-based RHPs transition from rod-like to random-walk statistics and ultimately collapse into compact globules stabilized by hydrophobic collapse and methacrylate-poly(ethylene glycol) (PEG) interactions. Positively charged monomers follow the Hofmeister series in their hydration. Interestingly, the dimerization results from…
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Taxonomy
TopicsHydrogels: synthesis, properties, applications · Polymer Surface Interaction Studies · Pickering emulsions and particle stabilization