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蛋白冠阻碍了 N-CQDs 的氧化能力,并有利于其作为纳米生物催化系统的应用。

Protein Corona Hinders N-CQDs Oxidative Potential and Favors Their Application as Nanobiocatalytic System.

机构信息

Department of Biochemistry, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Toruń, 87-100 Toruń, Poland.

Chair of Plant Physiology and Biotechnology, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Toruń, 87-100 Toruń, Poland.

出版信息

Int J Mol Sci. 2021 Jul 29;22(15):8136. doi: 10.3390/ijms22158136.

DOI:10.3390/ijms22158136
PMID:34360901
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8347256/
Abstract

The oxidative properties of nanomaterials arouse legitimate concerns about oxidative damage in biological systems. On the other hand, the undisputable benefits of nanomaterials promote them for biomedical applications; thus, the strategies to reduce oxidative potential are urgently needed. We aimed at analysis of nitrogen-containing carbon quantum dots (N-CQDs) in terms of their biocompatibility and internalization by different cells. Surprisingly, N-CQD uptake does not contribute to the increased oxidative stress inside cells and lacks cytotoxic influence even at high concentrations, primarily through protein corona formation. We proved experimentally that the protein coating effectively limits the oxidative capacity of N-CQDs. Thus, N-CQDs served as an immobilization support for three different enzymes with the potential to be used as therapeutics. Various kinetic parameters of immobilized enzymes were analyzed. Regardless of the enzyme structure and type of reaction catalyzed, adsorption on the nanocarrier resulted in increased catalytic efficiency. The enzymatic-protein-to-nanomaterial ratio is the pivotal factor determining the course of kinetic parameter changes that can be tailored for enzyme application. We conclude that the above properties of N-CQDs make them an ideal support for enzymatic drugs required for multiple biomedical applications, including personalized medical therapies.

摘要

纳米材料的氧化特性引起了人们对生物系统中氧化损伤的合理关注。另一方面,纳米材料不可否认的好处促使它们在生物医学中的应用;因此,迫切需要降低氧化潜力的策略。我们旨在分析含氮碳量子点(N-CQDs)在其生物相容性和不同细胞内化方面的特性。令人惊讶的是,N-CQD 的摄取不会导致细胞内氧化应激增加,即使在高浓度下也缺乏细胞毒性影响,主要是通过形成蛋白质外壳。我们通过实验证明,蛋白质涂层有效地限制了 N-CQDs 的氧化能力。因此,N-CQDs 可用作三种不同酶的固定化载体,具有作为治疗剂的潜力。分析了固定化酶的各种动力学参数。无论酶的结构和催化的反应类型如何,吸附在纳米载体上都会导致催化效率的提高。酶-蛋白质-纳米材料的比例是决定动力学参数变化过程的关键因素,可针对酶的应用进行调整。我们得出结论,N-CQDs 的上述特性使它们成为多种生物医学应用(包括个性化医疗疗法)所需酶类药物的理想载体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab9c/8347256/c5b49513aafc/ijms-22-08136-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab9c/8347256/dbc3952605df/ijms-22-08136-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab9c/8347256/43382bee749c/ijms-22-08136-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab9c/8347256/c5b49513aafc/ijms-22-08136-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab9c/8347256/dbc3952605df/ijms-22-08136-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ab9c/8347256/b3e48fd4798f/ijms-22-08136-g002.jpg
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