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细胞色素吸附在普朗尼克三嵌段共聚物稳定的MoS纳米片上形成的新型纳米生物催化系统的增强催化活性

Enhanced Catalytic Activity of a New Nanobiocatalytic System Formed by the Adsorption of Cytochrome on Pluronic Triblock Copolymer Stabilized MoS Nanosheets.

作者信息

Devassy Anu Maria Chittilappilly, Kamalakshan Adithya, Jamuna Nidhi Anilkumar, Ansilda Roselin, Mandal Sarthak

机构信息

Department of Chemistry, National Institute of Technology, Tiruchirappalli, Tamil Nadu 620015, India.

出版信息

ACS Omega. 2022 May 3;7(19):16593-16604. doi: 10.1021/acsomega.2c00839. eCollection 2022 May 17.

DOI:10.1021/acsomega.2c00839
PMID:35601299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9118411/
Abstract

The formation of nanobiohybrids through the immobilization of enzymes on functional nanomaterials has opened up exciting research opportunities at the nanobiointerfaces. These systems hold great promise for a wide range of applications in biosensing, biocatalytic, and biomedical fields. Here, we report the formation of a hybrid nanobiocatalytic system through the adsorption of cytochrome (Cyt ) on pluronic triblock copolymer, P123 (PEO--PPO--PEO), stabilized MoS nanosheets. The use of pluronic polymer has helped not only to greatly stabilize the exfoliated MoS nanosheets but also to allow easy adsorption of Cyt on the nanosheets without major structural changes due to its excellent biocompatibility and soft protein-binding property. By comparing the catalytic activity of the Cyt -MoS nanobiohybrid with that of the free Cyt and as-prepared MoS nanosheets, we have demonstrated the active role of the nanobiointeractions in enhancing the catalytic activity of the hybrid. Slight structural perturbation at the active site of the Cyt upon adsorption on MoS has primarily facilitated the peroxidase activity of the Cyt . As the MoS nanosheets and the native Cyt individually exhibit weaker intrinsic peroxidase activities, their mutual modulation at the nanobiointerface has made the Cyt -MoS a novel nanobiocatalyst with superior activity.

摘要

通过将酶固定在功能性纳米材料上形成纳米生物杂化物,为纳米生物界面带来了令人兴奋的研究机遇。这些系统在生物传感、生物催化和生物医学领域的广泛应用中具有巨大潜力。在此,我们报道了一种混合纳米生物催化系统的形成,该系统是通过细胞色素(Cyt)吸附在由普朗尼克三嵌段共聚物P123(PEO--PPO--PEO)稳定的MoS纳米片上形成的。使用普朗尼克聚合物不仅有助于极大地稳定剥离的MoS纳米片,还因其优异的生物相容性和软蛋白结合特性,使Cyt能够轻松吸附在纳米片上而不会发生重大结构变化。通过比较Cyt -MoS纳米生物杂化物与游离Cyt和制备好的MoS纳米片的催化活性,我们证明了纳米生物相互作用在增强杂化物催化活性方面的积极作用。Cyt吸附在MoS上时,其活性位点的轻微结构扰动主要促进了Cyt的过氧化物酶活性。由于MoS纳米片和天然Cyt单独表现出较弱的固有过氧化物酶活性,它们在纳米生物界面的相互调节使Cyt -MoS成为一种具有卓越活性的新型纳米生物催化剂。

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