Integrating Electrochemistry and Optical Imaging to Probe Phospholipid Architectures: Emerging Paradigms in Fluorescence and Electrochemiluminescence Studies

IF 6.7
Chemical & Biomedical Imaging Pub Date : 2026-06-22 Epub Date: 2026-01-26 DOI:10.1021/cbmi.5c00263
Fatma Ben Trad, Eric Labbé, Olivier Buriez
{"title":"Integrating Electrochemistry and Optical Imaging to Probe Phospholipid Architectures: Emerging Paradigms in Fluorescence and Electrochemiluminescence Studies","authors":"Fatma Ben Trad,&nbsp;Eric Labbé,&nbsp;Olivier Buriez","doi":"10.1021/cbmi.5c00263","DOIUrl":null,"url":null,"abstract":"<p>The interplay between electrochemistry and optical microscopy\r\nis\r\nredefining how complex interfacial processes are visualized and quantified\r\nat the nanoscale. Here, we review and contextualize emerging strategies\r\nthat integrate electrochemical control with fluorescence and electrochemiluminescence\r\n(ECL) imaging to probe phospholipid architectures, from supported\r\nlipid bilayers (SLBs) to liposomes or giant unilamellar vesicles (GUVs).\r\nIn fluorescence-based approaches, the combination of electrochemical\r\npotential modulation with high-resolution microscopy enables a direct\r\ncorrelation between redox activity and molecular organization within\r\nmembranes. Recent developments in total internal reflection fluorescence\r\nmicroscopy combined with electrochemical fluorescence microscopy (TIRF–ECFM)\r\nand redox-sensitive probes have revealed electrochemically induced\r\nlipid reorganization and redox processes within supported bilayers\r\nwith unprecedented sensitivity. Complementarily, ECL microscopy extends\r\nthis paradigm by exploiting light emission triggered by electron transfer\r\nat electrode interfaces, providing label-free and background-free\r\nimaging of lipid film integrity, membrane rupture, and peptide-induced\r\npermeabilization. Studies on ECL-active liposomes and SLBs demonstrate\r\nthat variations in emission onset and intensity directly report on\r\nthe local membrane composition, permeability, and electrostatics.\r\nMoreover, encapsulation of enzymatic + redox-active species within\r\nGUVs enables real-time, noninvasive ECL monitoring of confined biochemical\r\nreactions. Collectively, these emerging electro-optical methodologies\r\nestablish a versatile toolbox for dissecting membrane dynamics and\r\nbiochemical reactivity with molecular precision. Their convergence\r\nheralds an original analytical frontier at the interface of electrochemistry,\r\noptical imaging, and membrane biophysics, paving the way for next-generation\r\nbiosensing, drug screening, and single-vesicle electroanalysis.</p>","PeriodicalId":53181,"journal":{"name":"Chemical & Biomedical Imaging","volume":"4 6","pages":"1004–1017"},"PeriodicalIF":6.7000,"publicationDate":"2026-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical & Biomedical Imaging","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/cbmi.5c00263","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/26 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The interplay between electrochemistry and optical microscopy is redefining how complex interfacial processes are visualized and quantified at the nanoscale. Here, we review and contextualize emerging strategies that integrate electrochemical control with fluorescence and electrochemiluminescence (ECL) imaging to probe phospholipid architectures, from supported lipid bilayers (SLBs) to liposomes or giant unilamellar vesicles (GUVs). In fluorescence-based approaches, the combination of electrochemical potential modulation with high-resolution microscopy enables a direct correlation between redox activity and molecular organization within membranes. Recent developments in total internal reflection fluorescence microscopy combined with electrochemical fluorescence microscopy (TIRF–ECFM) and redox-sensitive probes have revealed electrochemically induced lipid reorganization and redox processes within supported bilayers with unprecedented sensitivity. Complementarily, ECL microscopy extends this paradigm by exploiting light emission triggered by electron transfer at electrode interfaces, providing label-free and background-free imaging of lipid film integrity, membrane rupture, and peptide-induced permeabilization. Studies on ECL-active liposomes and SLBs demonstrate that variations in emission onset and intensity directly report on the local membrane composition, permeability, and electrostatics. Moreover, encapsulation of enzymatic + redox-active species within GUVs enables real-time, noninvasive ECL monitoring of confined biochemical reactions. Collectively, these emerging electro-optical methodologies establish a versatile toolbox for dissecting membrane dynamics and biochemical reactivity with molecular precision. Their convergence heralds an original analytical frontier at the interface of electrochemistry, optical imaging, and membrane biophysics, paving the way for next-generation biosensing, drug screening, and single-vesicle electroanalysis.

整合电化学和光学成像探测磷脂结构:荧光和电化学发光研究的新范式。
电化学和光学显微镜之间的相互作用正在重新定义如何在纳米尺度上可视化和量化复杂的界面过程。在这里,我们回顾并介绍了将电化学控制与荧光和电化学发光(ECL)成像相结合的新兴策略,以探测磷脂结构,从支持脂质双层(slb)到脂质体或巨型单层囊泡(guv)。在基于荧光的方法中,电化学电位调制与高分辨率显微镜的结合使氧化还原活性与膜内分子组织之间的直接关联成为可能。全内反射荧光显微镜结合电化学荧光显微镜(TIRF-ECFM)和氧化还原敏感探针的最新发展,以前所未有的灵敏度揭示了电化学诱导的脂质重组和氧化还原过程。此外,ECL显微镜通过利用电极界面上电子转移引发的光发射来扩展这种范例,提供无标记和无背景的脂质膜完整性、膜破裂和肽诱导的渗透成像。对ecl活性脂质体和slb的研究表明,发射开始和强度的变化直接反映了局部膜的组成、通透性和静电。此外,将酶+氧化还原活性物质包封在guv内,可以实现对受限生化反应的实时、无创ECL监测。总的来说,这些新兴的光电方法建立了一个多功能工具箱,用于解剖膜动力学和具有分子精度的生化反应性。它们的融合预示着电化学、光学成像和膜生物物理学界面上的原始分析前沿,为下一代生物传感、药物筛选和单囊泡电分析铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Chemical & Biomedical Imaging
Chemical & Biomedical Imaging 化学与生物成像-
CiteScore
1.00
自引率
0.00%
发文量
0
期刊介绍: Chemical & Biomedical Imaging is a peer-reviewed open access journal devoted to the publication of cutting-edge research papers on all aspects of chemical and biomedical imaging. This interdisciplinary field sits at the intersection of chemistry physics biology materials engineering and medicine. The journal aims to bring together researchers from across these disciplines to address cutting-edge challenges of fundamental research and applications.Topics of particular interest include but are not limited to:Imaging of processes and reactionsImaging of nanoscale microscale and mesoscale materialsImaging of biological interactions and interfacesSingle-molecule and cellular imagingWhole-organ and whole-body imagingMolecular imaging probes and contrast agentsBioluminescence chemiluminescence and electrochemiluminescence imagingNanophotonics and imagingChemical tools for new imaging modalitiesChemical and imaging techniques in diagnosis and therapyImaging-guided drug deliveryAI and machine learning assisted imaging
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书