In this study, we demonstrate that an aromatic oligoamide sequence assembles into a trimeric helix-turn-helix architecture with a disulfide linkage, and upon cleavage of this linkage, it reconstructs into an antiparallel double helix. The antiparallel double helix is accessible to encapsulate a diacid guest within its cavity, forming a 2:1 host–guest complex. In contrast, hydrogen-bonding interactions between the trimeric-assembled structure and guests induce a conformational shift in the trimeric helix, resulting in a cross-shaped double-helix complex at a 2:2 host–guest ratio. Interconversions between the trimeric helix and the antiparallel double helix, along with their respective host–guest complexes, can be initiated through thiol/disulfide redox-mediated regulation.
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Yu et al. (2024) studied this question.
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