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利用自组装技术的万花筒大分子合成与应用。

Kaleidoscope megamolecules synthesis and application using self-assembly technology.

作者信息

Zhou Shengwang, Wei Yuan

机构信息

School of Pharmacy, Jiangsu University, Zhenjiang 212013, PR China.

School of Pharmacy, Jiangsu University, Zhenjiang 212013, PR China.

出版信息

Biotechnol Adv. 2023 Jul-Aug;65:108147. doi: 10.1016/j.biotechadv.2023.108147. Epub 2023 Apr 5.

DOI:10.1016/j.biotechadv.2023.108147
PMID:37023967
Abstract

The megamolecules with high ordered structures play an important role in chemical biology and biomedical engineering. Self-assembly, a long-discovered but very appealing technique, could induce many reactions between biomacromolecules and organic linking molecules, such as an enzyme domain and its covalent inhibitors. Enzyme and its small-molecule inhibitors have achieved many successes in medical application, which realize the catalysis process and theranostic function. By employing the protein engineering technology, the building blocks of enzyme fusion protein and small molecule linker can be assembled into a novel architecture with the specified organization and conformation. Molecular level recognition of enzyme domain could provide both covalent reaction sites and structural skeleton for the functional fusion protein. In this review, we will discuss the range of tools available to combine functional domains by using the recombinant protein technology, which can assemble them into precisely specified architectures/valences and develop the kaleidoscope megamolecules for catalytic and medical application.

摘要

具有高度有序结构的大分子在化学生物学和生物医学工程中发挥着重要作用。自组装是一项早就被发现但极具吸引力的技术,它能引发生物大分子与有机连接分子之间的许多反应,比如酶结构域及其共价抑制剂之间的反应。酶及其小分子抑制剂在医学应用中已取得诸多成功,实现了催化过程和诊疗功能。通过运用蛋白质工程技术,酶融合蛋白和小分子连接体的构建模块可组装成具有特定组织和构象的新型结构。酶结构域的分子水平识别可为功能性融合蛋白提供共价反应位点和结构骨架。在本综述中,我们将讨论利用重组蛋白技术来组合功能结构域的一系列可用工具,这些工具能将它们组装成精确指定的结构/价态,并开发出用于催化和医学应用的千变万化的大分子。

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