Liu Xiaofeng, Qin Jinan, Zhang Xiaoyu, Zou Liyuan, Yang Xiaohai, Wang Qing, Zheng Yan, Mei Wenjing, Wang Kemin
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha 410082, China.
Nanoscale. 2020 Dec 21;12(47):24206-24213. doi: 10.1039/d0nr05732k. Epub 2020 Dec 8.
Nanozymes have drawn increasing attention with their broad applications but most nanozymes lack enzyme-like molecular structures, resulting in weak selectivity and low activity. Bioinspired molecular assembly provides an extremely promising strategy to mimic natural enzyme processes and develop function enhanced architectures. Herein, a new bioinspired molecular assembly strategy based on human serum albumin@polydopamine/Fe nanocomposites (HSA@PDA/Fe NCs) was proposed, in which Fe(iii)/Fe(ii) were anchored on HSA supported on PDA. HSA@PDA/Fe NCs with iron as the active center and HSA@PDA as the skeleton showed excellent peroxidase-like activity, which was nearly 1000 times higher than that of free Fe(iii). This may be attributed to the phenomenon that the cycle of quinones and the hydroxyl group on the nanocomposite surface greatly accelerate the conversion of Fe(iii)/Fe(ii) in acidic microenvironments. Systematic experimental studies illustrated that its activity was mainly affected by the metal active center, followed by the polymeric ligand, while the protein framework has little effect on its activity. Meanwhile, even after freeze-thaw and thermal cycle tests, it also showed excellent catalytic stability. Besides, a colorimetric assay based on HSA@PDA/Fe NCs was developed for detection of HOin vitro and in situ detection of HO generated from live cells. This work will facilitate the developments on theoretical analysis, rational design and practical applications of nanozymes based on bioinspired molecular assemblies.
纳米酶因其广泛的应用而受到越来越多的关注,但大多数纳米酶缺乏类似酶的分子结构,导致选择性弱和活性低。受生物启发的分子组装为模拟天然酶过程和开发功能增强的结构提供了一种极具前景的策略。在此,提出了一种基于人血清白蛋白@聚多巴胺/铁纳米复合材料(HSA@PDA/Fe NCs)的新型受生物启发的分子组装策略,其中Fe(iii)/Fe(ii)锚定在PDA负载的HSA上。以铁为活性中心、HSA@PDA为骨架的HSA@PDA/Fe NCs表现出优异的过氧化物酶样活性,比游离Fe(iii)的活性高出近1000倍。这可能归因于纳米复合材料表面醌和羟基的循环在酸性微环境中极大地加速了Fe(iii)/Fe(ii)的转化这一现象。系统的实验研究表明,其活性主要受金属活性中心影响,其次是聚合物配体,而蛋白质框架对其活性影响较小。同时即使经过冻融和热循环测试,它也表现出优异的催化稳定性。此外,还开发了一种基于HSA@PDA/Fe NCs的比色法用于体外检测H₂O₂以及原位检测活细胞产生的H₂O₂。这项工作将促进基于受生物启发的分子组装的纳米酶在理论分析、合理设计和实际应用方面的发展。