Self-Assembled DNA/Peptide-Based Nanoparticle Exhibiting Synergistic Enzymatic Activity

被引:76
作者
Liu, Qing [1 ,2 ]
Wang, Hui [1 ]
Shi, Xinghua [1 ,2 ]
Wang, Zhen-Gang [1 ]
Ding, Baoquan [1 ,2 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Nanosyst & Hierarchial Fabricat, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
美国国家科学基金会;
关键词
DNA; peptide; hemin; peroxidase mimics; self-assembly; QUANTUM-MECHANICAL CALCULATIONS; CYTOCHROME-C; HORSERADISH-PEROXIDASE; M(CO)(6) M=CR; IN-VITRO; SUPRAMOLECULAR CATALYSIS; MOLECULAR SIMULATION; HIGHLY EFFICIENT; HIGH-THROUGHPUT; BINDING-SITE;
D O I
10.1021/acsnano.7b03195
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Designing enzyme-mimicking active sites in artificial systems is key to achieving catalytic efficiencies rivaling those of natural enzymes and can provide valuable insight in the understanding of the natural evolution of enzymes. Here, we report the design of a catalytic hemin-containing nanoparticle with self-assembled guanine-rich nucleic acid/histidine-rich peptide components that mimics the active site and peroxidative activity of hemoproteins. The chemical complementarities between the folded nucleic acid and peptide enable the spatial arrangement of essential elements in the active site and effective activation of hemin. As a result, remarkable synergistic effects of nucleic acid and peptide on the catalytic performances were observed. The turnover number of peroxide reached the order of that of natural peroxidase, and the catalytic efficiency is comparable to that of myoglobin. These results have implications in the precise design of supramolecular enzyme mimetics, particularly those with hierarchical active sites. The assemblies we describe here may also resemble an intermediate in the evolution of contemporary enzymes from the catalytic RNA of primitive cells.
引用
收藏
页码:7251 / 7258
页数:8
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