Issue 35, 2017

Multiscale simulations for understanding the evolution and mechanism of hierarchical peptide self-assembly

Abstract

Hierarchical self-assembly, abundant in biological systems, has been explored as an effective bottom-up method to fabricate highly ordered functional superstructures from elemental building units. Biomolecules, especially short peptides consisting of several amino acids, are a type of elegant building blocks due to their advantages of structural, mechanical, and functional diversity as well as high biocompatibility and biodegradability. The hierarchical self-assembly of peptides is a spontaneous process spanning multiple time and length scales under certain thermodynamics and kinetics conditions. Therefore, understanding the mechanisms of dynamic processes is crucial to directing the construction of complicated biomimetic systems with multiple functionalities. Multiscale molecular simulations that combine and systematically link several hierarchies can provide insights into the evolution and dynamics of hierarchical self-assembly from the molecular level to the mesoscale. Herein, we provided an overview of the simulation hierarchies in the general field of peptide self-assembly modeling. In particular, we highlighted multiscale simulations for unraveling the mechanisms underlying the dynamic self-assembly process with an emphasis on weak intermolecular interactions in the process stages and the energies of different molecular alignments as well as the role of thermodynamic and kinetic factors at the microscopic level.

Graphical abstract: Multiscale simulations for understanding the evolution and mechanism of hierarchical peptide self-assembly

Article information

Article type
Perspective
Submitted
26 мар 2017
Accepted
09 май 2017
First published
09 май 2017

Phys. Chem. Chem. Phys., 2017,19, 23614-23631

Multiscale simulations for understanding the evolution and mechanism of hierarchical peptide self-assembly

C. Yuan, S. Li, Q. Zou, Y. Ren and X. Yan, Phys. Chem. Chem. Phys., 2017, 19, 23614 DOI: 10.1039/C7CP01923H

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