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Fabrication of Raspberry-like Cytochrome C Surface-Imprinted Nanoparticles Based on MOF Composites for High-Performance Protein Separation

材料科学 制作 吸附 分散性 纳米颗粒 细胞色素c 复合材料 单体 化学工程 分子印迹聚合物 金属有机骨架 聚合物 纳米技术 分子印迹 选择性 有机化学 高分子化学 催化作用 化学 病理 工程类 医学 生物化学 替代医学 线粒体
作者
Liwei Qian,Wenqian Liu,Hanbin Liu,Valentin Nica,Sufeng Zhang,Qiusheng Zhou,Wenqi Song,Qiuyu Zhang
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:13 (26): 31010-31020 被引量:35
标识
DOI:10.1021/acsami.1c07107
摘要

The development of high-performance protein-imprinted materials is vital to meet the requirements of proteomics research but remains a challenge. Herein, a new type of raspberry-like cytochrome C-imprinted nanoparticle was first designed and fabricated via surface imprinting technology combined with a template immobilization strategy. In particular, the state-of-the-art metal–organic framework (MOF)/carbon nanoparticle (CN) composites were selected as protein immobilization carriers for two advantages: (1) the composites reflected the intrinsic characteristics of MOFs including flexible design, facile preparation, and extensive interactions with proteins and (2) the utilization of composites also overcame the issue associated with the severe agglomeration of individual MOFs during the post-use process. Therefore, the as-prepared composites exhibited a regular raspberry-like shape with good dispersion (polydispersity index (PDI) < 0.25), high specific surface area (551.4 m2 g–1), and outstanding cytochrome C immobilization capacity (900 mg g–1). Furthermore, a zwitterionic monomer was chosen to participate in the synthesis of an imprinting layer to reduce the nonspecific binding with proteins. As a result, the unique design presented here in both the protein immobilization carrier and the selected polymer composition endowed the imprinted material (noted as CN@UIO-66@MIPs) with the excellent ability for cytochrome C enrichment with extremely high recognition ability (imprinting factor (IF) = 6.1), rapid adsorption equilibrium time (40 min), and large adsorption capacity (815 mg g–1). Furthermore, encouraged by the experimental results, we successfully used CN@UIO-66@MIPs to specifically capture cytochrome C in mixed protein solutions and biological samples, which proved them to be a potential candidate for protein separation and purification.
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