Department of Biocatalysis, Institute of Catalysis (CSIC), c/Marie curie 2, Cantoblanco Campus UAM, 28049 Madrid, Spain.
Instituto de Biocomputación y Física de Sistemas Complejos, Joint Units IQFR-CSIC-BIFI, and GBsC-CSIC-BIFI, Universidad de Zaragoza, 50009 Zaragoza, Spain.
ACS Appl Mater Interfaces. 2021 Feb 3;13(4):5111-5124. doi: 10.1021/acsami.0c20501. Epub 2021 Jan 20.
Artificial enzymes with modulated enzyme-mimicking activities of natural systems represent a challenge in catalytic applications. Here, we show the creation of artificial Cu metalloenzymes based on the generation of Cu nanoparticles in an enzyme matrix. Different enzymes were used, and the structural differences between the enzymes especially influenced the controlled the size of the nanoparticles and the environment that surrounds them. Herein, we demonstrated that the oxidase-like catalytic activity of these copper nanozymes was rationally modulated by enzyme used as a scaffold, with a special role in the nanoparticle size and their environment. In this sense, these nanocopper hybrids have confirmed the ability to mimic a unique enzymatic activity completely different from the natural activity of the enzyme used as a scaffold, such as tyrosinase-like activity or as Fenton catalyst, which has extremely higher stability than natural mushroom tyrosinase. More interestingly, the oxidoreductase-like activity of nanocopper hybrids was cooperatively modulated with the synergistic effect between the enzyme and the nanoparticles improving the catalase activity (no peroxidase activity). Additionally, a novel dual (metallic and enzymatic activity) of the nanozyme made the highly improved catechol-like activity interesting for the design of 3,4-dihydroxy-l-phenylalanine (l-DOPA) biosensor for detection of tyrosinase. These hybrids also showed cytotoxic activity against different tumor cells, interesting in biocatalytic tumor therapy.
基于在酶基质中生成 Cu 纳米颗粒,人工 Cu 金属酶被设计用来模拟天然系统的酶促反应。不同的酶被用来控制纳米颗粒的大小和周围环境,而酶的结构差异对其产生了重要影响。在此,我们证明了这些铜纳米酶的氧化酶样催化活性可以通过用作支架的酶进行合理调节,而酶在纳米颗粒的大小及其环境中起着特殊作用。从这个意义上说,这些纳米铜杂化物具有模拟完全不同于用作支架的酶的天然活性的独特酶活性的能力,例如酪氨酸酶样活性或作为芬顿催化剂的活性,其稳定性比天然蘑菇酪氨酸酶高得多。更有趣的是,纳米铜杂化物的氧化还原酶样活性与酶和纳米颗粒之间的协同作用协同调节,从而提高了过氧化氢酶活性(无过氧化物酶活性)。此外,纳米酶的新型双重(金属和酶活性)使其对设计用于检测酪氨酸酶的 3,4-二羟基-l-苯丙氨酸(l-DOPA)生物传感器的儿茶酚样活性具有高度改善作用。这些杂化物还对不同的肿瘤细胞表现出细胞毒性活性,这在生物催化肿瘤治疗中很有趣。