Programmable α-Helices Enable Multiple Shape Memory in Peptides

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Authors: Kunpeng Wei, Jiangyan Shi, Renjie Wang, Chongyi Chen
Cited by: 2
References: 60

Abstract

Multiple shape memory polymers (multi-SMPs) can store multiple temporary shapes in a single cycle, offering enhanced adaptability in complex environments. Yet, most multi-SMPs rely on sophisticated copolymer designs to create discrete transition domains, limiting their simplicity and scalability. Here, we report homopeptide films with either α-helical or random-coil conformations that display distinct shape memory behaviors. Remarkably, α-helical films encode at least six thermally actuated shapes enabled by their programmable helices. The rod-like helices confer superior thermal stability and drive ordered lattice formation, leading to two broad thermoresponsive transitions associated with the glass transition and lattice reorganization. In addition, the noncovalent nature of the peptide films affords efficient healing. This chemically straightforward yet functionally versatile strategy provides a scalable platform for the development of next-generation shape-morphing materials.

Fields of Study & Subjects

Supramolecular Self-Assembly in Materials Polymer composites and self-healing Chemical Synthesis and Analysis

Publication details

Journal / source
Macromolecules
Publisher
American Chemical Society (ACS)
Volume
59
Issue
5
Pages
3063–3071
Publication date
25 February 2026
Language
EN