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基于电活性分子印迹聚合物的蛋白质传感器的制备策略:牛血清白蛋白和胰蛋白酶传感的实例。

A fabrication strategy for protein sensors based on an electroactive molecularly imprinted polymer: Cases of bovine serum albumin and trypsin sensing.

机构信息

Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, Jiangsu Province, 214122, PR China.

International Joint Research Center for Photoresponsive Molecules and Materials, Jiangnan University, 1800 Lihu Avenue, Wuxi, Jiangsu Province, 214122, PR China.

出版信息

Anal Chim Acta. 2020 Jun 22;1117:25-34. doi: 10.1016/j.aca.2020.04.023. Epub 2020 Apr 13.

Abstract

A high-performance molecularly imprinted sensing platform inspired by natural recognition mechanisms was fabricated to detect protein by employing a linear electro-polymerizable molecularly imprinted polymer as macromonomer. This was achieved via the combination of a biosensor fabrication with a self-assembly imprinting technique without the use of chemical labels. An amphipathic electroactive copolymer was designed as macro-monomer to maintain structural integrity of the protein template via self-assembly, resulting in generation of a 3D construction around the protein molecule to form imprinted sites. Electro-polymerization was utilized not only to anchor imprinted sites but also to enhance electron transfer. The adaptable sensing platform was based on a strengthened recognition reaction between the MIP layer and template protein after the generation of an electroactive network. Bovine serum albumin (BSA) and trypsin were used as model proteins to investigate the method's generality, which gave broad detection ranges of 10-10 mg mL for BSA and 10-10 mg mL for trypsin. These results indicate that the proposed fabrication offers an effective and versatile strategy for protein recognition.

摘要

受自然识别机制启发,我们构建了一种高性能的分子印迹传感平台,通过使用线性电聚合分子印迹聚合物作为大分子单体来检测蛋白质。这是通过将生物传感器制造与自组装印迹技术相结合来实现的,而无需使用化学标记物。设计了一种两亲性电活性共聚物作为大分子单体,通过自组装来保持蛋白质模板的结构完整性,从而在蛋白质分子周围产生 3D 结构以形成印迹位点。电聚合不仅用于固定印迹位点,还用于增强电子转移。适应性传感平台基于在形成电活性网络后 MIP 层与模板蛋白质之间的强化识别反应。牛血清白蛋白(BSA)和胰蛋白酶被用作模型蛋白质来研究该方法的通用性,其对 BSA 的检测范围为 10-10 mg mL,对胰蛋白酶的检测范围为 10-10 mg mL。这些结果表明,所提出的制造方法为蛋白质识别提供了一种有效且通用的策略。

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