排列溶菌酶蛋白原纤维自组装压电薄膜。

IF 5.5 2区 化学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Biomacromolecules Pub Date : 2025-01-13 Epub Date: 2025-01-02 DOI:10.1021/acs.biomac.4c01305
Donn Adam D Gito, Alireza Akbarinejad, Alexander Dixon, Thomas Loho, Michel Nieuwoudt, Qun Chen, Laura J Domigan, Jenny Malmström
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引用次数: 0

摘要

压电有机聚合物具有机械柔韧性,因此适合用于柔性和可穿戴压电设备,是无机聚合物的理想替代品。据报道,蛋白质等生物聚合物具有压电性,同时还具有生物相容性和生物可降解性等其他优点。然而,有关蛋白质压电性的问题依然存在,例如蛋白质二级结构的影响。本研究探讨了溶菌酶淀粉样蛋白纤维薄膜的压电特性,该薄膜由聚乙二醇 (PEG) 塑化而成。在优化的 PEG 浓度下,薄膜显示出 1.4 ± 0.1 pCN-1 的可测量 d33 系数,证实了压电性。研究发现,PEG 与纤维发生氢键结合,可能会影响薄膜的压电响应。偏振成像显示,淀粉样蛋白纤维呈圆周排列的长程排列。这些结果表明,利用淀粉样蛋白纤维(可由各种蛋白质形成)制造块状自组装压电材料具有很大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Self-Assembled Piezoelectric Films from Aligned Lysozyme Protein Fibrils.

Piezoelectric organic polymers are promising alternatives to their inorganic counterparts due to their mechanical flexibility, making them suitable for flexible and wearable piezoelectric devices. Biological polymers such as proteins have been reported to possess piezoelectricity, while offering additional benefits, such as biocompatibility and biodegradability. However, questions remain regarding protein piezoelectricity, such as the impact of the protein secondary structure. This study examines the piezoelectric properties of lysozyme amyloid fibril films, plasticized by polyethylene glycol (PEG). The films demonstrated a measurable d33 coefficient of 1.4 ± 0.1 pCN-1, for the optimized PEG concentration, confirming piezoelectricity. The PEG was found to hydrogen-bond with the fibrils, likely impacting the piezoelectric response of the film. Polarization imaging revealed long-range alignment of the amyloid fibrils in a circumferential arrangement. These results demonstrate the potential of using amyloid fibrils, which can be formed from various proteins, to create bulk self-assembled piezoelectric materials.

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来源期刊
Biomacromolecules
Biomacromolecules 化学-高分子科学
CiteScore
10.60
自引率
4.80%
发文量
417
审稿时长
1.6 months
期刊介绍: Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine. Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.
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