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同质氧化石墨烯-肽纳米纤维杂化水凝胶作为仿生多糖水解酶。

Homogenous graphene oxide-peptide nanofiber hybrid hydrogel as biomimetic polysaccharide hydrolase.

机构信息

Key Laboratory of Food Nutrition and Safety, Ministry of Education of China, Tianjin University of Science and Technology, Tianjin 300457, China.

出版信息

Nanoscale. 2017 Nov 23;9(45):18066-18074. doi: 10.1039/c7nr06525f.

Abstract

Cellulose, an impressive potential sustainable fuel, is difficult to hydrolyze because of the protection of β-1,4-glycosidic bonds through the tight hydrogen bonding network. In this study, homogenous graphene oxide (GO)-peptide nanofiber hybrid hydrogels (GO-PNFs) were designed as a β-glycosyl hydrolase mimetic to achieve efficient degradation of cellobiose and cellopentaose. For comparison, free peptides, graphene oxide mixed with free peptides (GO-peptdies) and self-assembled peptide nanofibers (PNFs) were also studied for their activity as a hydrolase mimetics for degradation of cellobiose. Among these materials, GO-PNFs showed the highest hydrolysis activity. Transmission electron microscopy, atomic force microscopy, fluorescence analysis, circular dichroism spectroscopies, X-ray diffraction, Raman spectra and computational modeling were used to interpret the difference in activity mechanism in these artificially designed enzymes. These investigations suggested that high catalytic performance of GO-PNFs toward cellobiose and cellopentaose hydrolysis could be attributed to the formation of nanofiber structures of peptides, optimal molecular conformation and less steric hindrance to access the substrate. More importantly, GO not only served as a platform for attaching PNFs, but also created a hydrophobic microenvironment and facilitated proton transfer, an essential step in catalytic hydrolysis, thus enhancing catalytic activity. All these provided insights into the potential use of peptides and GO hybrid composite nanoenzymes in efficient cellulose hydrolysis.

摘要

纤维素是一种很有前途的可持续燃料,但由于β-1,4-糖苷键受到紧密氢键网络的保护,所以很难水解。在这项研究中,设计了均相氧化石墨烯(GO)-肽纳米纤维杂化水凝胶(GO-PNFs)作为β-糖苷水解酶模拟物,以实现对纤维二糖和纤维五糖的有效降解。为了进行比较,还研究了游离肽、氧化石墨烯与游离肽混合(GO-peptdies)和自组装肽纳米纤维(PNFs)作为水解酶模拟物对纤维二糖的降解活性。在这些材料中,GO-PNFs 显示出最高的水解活性。透射电子显微镜、原子力显微镜、荧光分析、圆二色光谱、X 射线衍射、拉曼光谱和计算建模用于解释这些人工设计的酶在活性机制上的差异。这些研究表明,GO-PNFs 对纤维二糖和纤维五糖水解具有高催化性能,这归因于肽的纳米纤维结构的形成、最佳的分子构象和对底物的较少空间位阻。更重要的是,GO 不仅作为附着 PNFs 的平台,还创造了疏水环境并促进质子转移,这是催化水解的关键步骤,从而增强了催化活性。所有这些都为肽和 GO 杂化复合纳米酶在高效纤维素水解中的潜在应用提供了思路。

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