Enzymatic polymerization of enantiomeric L−3,4-dihydroxyphenylalanine into films with enhanced rigidity and stability
Yuhe Shen,
Rongxin Su,
Dongzhao Hao,
Xiaojian Xu,
Meital Reches,
Jiwei Min,
Heng Chang,
Tao Yu,
Qing Li,
Xiaoyu Zhang,
Yuefei Wang (),
Yuefei Wang () and
Wei Qi ()
Additional contact information
Yuhe Shen: Tianjin University
Rongxin Su: Tianjin University
Dongzhao Hao: Tianjin University
Xiaojian Xu: Tianjin University
Meital Reches: Institute of Chemistry, the Hebrew University
Jiwei Min: Tianjin University
Heng Chang: Tianjin University
Tao Yu: Tianjin University
Qing Li: Tianjin University
Xiaoyu Zhang: Tianjin University of Traditional Chinese Medicine
Yuefei Wang: Tianjin University of Traditional Chinese Medicine
Yuefei Wang: Tianjin University
Wei Qi: Tianjin University
Nature Communications, 2023, vol. 14, issue 1, 1-13
Abstract:
Abstract L−3,4-dihydroxyphenylalanine is an important molecule in the adhesion of mussels, and as an oxidative precursor of natural melanin, it plays an important role in living system. Here, we investigate the effect of the molecular chirality of 3,4-dihydroxyphenylalanine on the properties of the self-assembled films by tyrosinase-induced oxidative polymerization. The kinetics and morphology of pure enantiomers are completely altered upon their co-assembly, allowing the fabrication of layer-to-layer stacked nanostructures and films with improved structural and thermal stability. The different molecular arrangements and self-assembly mechanisms of the L+D-racemic mixtures, whose oxidation products have increased binding energy, resulting in stronger intermolecular forces, which significantly increases the elastic modulus. This study provides a simple pathway for the fabrication of biomimetic polymeric materials with enhanced physicochemical properties by controlling the chirality of monomers.
Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-38845-3
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DOI: 10.1038/s41467-023-38845-3
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