Charge-Dependent Fluorescence Lifetime Modulation in a Plasmonic Nanocavity

IF 4.6 2区 化学 Q2 CHEMISTRY, PHYSICAL
Alexey I. Chizhik, , , Damir I. Sakhapov, , , Ingo Gregor, , , Narain Karedla, , and , Jörg Enderlein*, 
{"title":"Charge-Dependent Fluorescence Lifetime Modulation in a Plasmonic Nanocavity","authors":"Alexey I. Chizhik,&nbsp;, ,&nbsp;Damir I. Sakhapov,&nbsp;, ,&nbsp;Ingo Gregor,&nbsp;, ,&nbsp;Narain Karedla,&nbsp;, and ,&nbsp;Jörg Enderlein*,&nbsp;","doi":"10.1021/acs.jpclett.5c01972","DOIUrl":null,"url":null,"abstract":"<p >Electric charges play a fundamental role in shaping the structure, function, and interactions of biomolecules, yet precisely measuring these charges at the single-molecule level remains a significant technical challenge. Here, we introduce a novel experimental methodology that utilizes plasmonic nanocavities to quantify molecular electric charges in solution with high sensitivity. Our approach exploits an externally applied electric field to induce the spatial redistribution of charged molecules confined within a planar metallic nanocavity while simultaneously leveraging nanocavity-induced fluorescence lifetime modulation as a highly sensitive readout. We demonstrate the feasibility of this method through proof-of-concept experiments, where we measure the fluorescence lifetimes of positively and negatively charged fluorescent dye molecules as a function of the applied electric field across the cavity. The experimental results are validated through a rigorous theoretical framework, incorporating statistical thermodynamics and electrodynamic modeling to accurately describe the observed data. The proposed method offers a calibration-free, experimentally simple, and rapid alternative to existing charge measurement techniques, opening new avenues for precise quantification of molecular electric charges down to the single-molecule level.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":"16 38","pages":"9900–9905"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jpclett.5c01972","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Electric charges play a fundamental role in shaping the structure, function, and interactions of biomolecules, yet precisely measuring these charges at the single-molecule level remains a significant technical challenge. Here, we introduce a novel experimental methodology that utilizes plasmonic nanocavities to quantify molecular electric charges in solution with high sensitivity. Our approach exploits an externally applied electric field to induce the spatial redistribution of charged molecules confined within a planar metallic nanocavity while simultaneously leveraging nanocavity-induced fluorescence lifetime modulation as a highly sensitive readout. We demonstrate the feasibility of this method through proof-of-concept experiments, where we measure the fluorescence lifetimes of positively and negatively charged fluorescent dye molecules as a function of the applied electric field across the cavity. The experimental results are validated through a rigorous theoretical framework, incorporating statistical thermodynamics and electrodynamic modeling to accurately describe the observed data. The proposed method offers a calibration-free, experimentally simple, and rapid alternative to existing charge measurement techniques, opening new avenues for precise quantification of molecular electric charges down to the single-molecule level.

Abstract Image

等离子体纳米腔中电荷依赖的荧光寿命调制。
电荷在形成生物分子的结构、功能和相互作用方面起着重要作用,然而在单分子水平上精确测量这些电荷仍然是一个重大的技术挑战。在这里,我们介绍了一种新的实验方法,利用等离子体纳米空腔以高灵敏度定量溶液中的分子电荷。我们的方法利用外部外加电场诱导平面金属纳米腔内带电分子的空间再分布,同时利用纳米腔诱导的荧光寿命调制作为高灵敏度读出。我们通过概念验证实验证明了这种方法的可行性,在实验中,我们测量了带正电和负电的荧光染料分子的荧光寿命,作为施加在整个腔中的电场的函数。实验结果通过严格的理论框架进行验证,结合统计热力学和电动力学建模来准确描述观测数据。所提出的方法提供了一种无需校准、实验简单、快速的替代现有电荷测量技术的方法,为精确定量分子电荷到单分子水平开辟了新的途径。
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
The Journal of Physical Chemistry Letters
The Journal of Physical Chemistry Letters CHEMISTRY, PHYSICAL-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
9.60
自引率
7.00%
发文量
1519
审稿时长
1.6 months
期刊介绍: The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.
×
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