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用于膜氧化还原酶生物电化学的固体支撑聚合物-脂质混合膜。

Solid-supported polymer-lipid hybrid membrane for bioelectrochemistry of a membrane redox enzyme.

作者信息

Catania Rosa, Heath George R, Rappolt Michael, Muench Stephen P, Beales Paul A, Jeuken Lars J C

机构信息

School of Chemistry, University of Leeds Leeds LS2 9JT UK

Astbury Centre for Structural Molecular Biology, University of Leeds Leeds LS2 9JT UK.

出版信息

RSC Appl Interfaces. 2025 Feb 11;2(3):665-672. doi: 10.1039/d4lf00362d. eCollection 2025 May 14.

DOI:10.1039/d4lf00362d
PMID:39980607
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11834424/
Abstract

Hybrid membranes, consisting of phospholipids and amphiphilic block polymers, offer enhanced stability compared to liposomes and greater biocompatibility than polymersomes. These qualities make them a versatile platform for a wide range of applications across various fields. In this study, we have investigated the ability of solid-supported polymer-lipid hybrid membranes (SSHM) to act as a platform for bioelectrochemistry of membrane proteins. The redox enzyme, cytochrome (cyt ), a terminal oxidase in , was reconstituted into hybrid vesicles (HVs), which were subsequently tested for their ability to form SSHMs on different self-assembled monolayers (SAMs) on gold electrodes. SSHM formation was monitored with electrochemical impedance spectroscopy (EIS), quartz crystal microbalance with dissipation (QCM-D), and atomic force microscopy (AFM). SSHMs were successfully formed on gold electrodes with mixed SAMs of 6-mercapto-1-hexanol and 1-hexanethiol at a 1 : 1 ratio. The activity of cyt was confirmed using cyclic voltammetry (CV), with electron transfer to cyt mediated by a lipophilic substrate-analogue decylubiquinone (DQ). SSHMs formed with HVs-cyt samples, stored for more than one year before use, remain bioelectrocatalytically active, confirming our previously established longevity and stability of HV systems.

摘要

由磷脂和两亲性嵌段聚合物组成的混合膜,与脂质体相比具有更高的稳定性,与聚合物囊泡相比具有更好的生物相容性。这些特性使其成为跨领域广泛应用的通用平台。在本研究中,我们研究了固体支持的聚合物 - 脂质混合膜(SSHM)作为膜蛋白生物电化学平台的能力。氧化还原酶细胞色素c(cyt c),作为呼吸链中的末端氧化酶,被重组到混合囊泡(HV)中,随后测试其在金电极上不同自组装单分子层(SAM)上形成SSHM的能力。用电化学阻抗谱(EIS)、耗散型石英晶体微天平(QCM - D)和原子力显微镜(AFM)监测SSHM的形成。在金电极上成功形成了由6 - 巯基 - 1 - 己醇和1 - 己硫醇以1∶1比例组成的混合SAM的SSHM。使用循环伏安法(CV)确认了cyt c的活性,电子通过亲脂性底物类似物癸基泛醌(DQ)介导转移到cyt c。由HVs - cyt c样品形成的SSHM,在使用前储存了一年多,仍保持生物电催化活性,证实了我们之前建立的HV系统的寿命和稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/daa30fc5efde/d4lf00362d-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/321a5d1affbe/d4lf00362d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/2cbee180f0f4/d4lf00362d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/075dec25744e/d4lf00362d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/28cb23ca935c/d4lf00362d-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/daa30fc5efde/d4lf00362d-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/321a5d1affbe/d4lf00362d-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/2cbee180f0f4/d4lf00362d-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/075dec25744e/d4lf00362d-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/28cb23ca935c/d4lf00362d-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e938/11834424/daa30fc5efde/d4lf00362d-f5.jpg

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