Evidence for a transfer-to-trap mechanism of fluorophore concentration quenching in lipid bilayers.

IF 3.2 3区 生物学 Q2 BIOPHYSICS
Biophysical journal Pub Date : 2024-09-17 Epub Date: 2024-07-22 DOI:10.1016/j.bpj.2024.07.026
Sophie A Meredith, Yuka Kusunoki, Stephen D Evans, Kenichi Morigaki, Simon D Connell, Peter G Adams
{"title":"Evidence for a transfer-to-trap mechanism of fluorophore concentration quenching in lipid bilayers.","authors":"Sophie A Meredith, Yuka Kusunoki, Stephen D Evans, Kenichi Morigaki, Simon D Connell, Peter G Adams","doi":"10.1016/j.bpj.2024.07.026","DOIUrl":null,"url":null,"abstract":"<p><p>It is important to understand the behaviors of fluorescent molecules because, firstly, they are often utilized as probes in biophysical experiments and, secondly, they are crucial cofactors in biological processes such as photosynthesis. A phenomenon called \"fluorescence quenching\" occurs when fluorophores are present at high concentrations, but the mechanisms for quenching are debated. Here, we used a technique called \"in-membrane electrophoresis\" to generate concentration gradients of fluorophores within a supported lipid bilayer, across which quenching was expected to occur. Fluorescence lifetime imaging microscopy (FLIM) provides images where the fluorescence intensity in each pixel is correlated to fluorescence lifetime: the intensity provides information about the location and concentration of fluorophores and the lifetime reveals the occurrence of energy-dissipative processes. FLIM was used to compare the quenching behavior of three commonly used fluorophores: Texas Red (TR), nitrobenzoaxadiazole (NBD), and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY). FLIM images provided evidence of quenching in regions where the fluorophores accumulated, but the degree of quenching varied between the different fluorophores. The relationship between quenching and concentration was quantified and the \"critical radius for trap formation,\" representing the relative quenching strength, was calculated as 2.70, 2.02, and 1.14 nm, for BODIPY, TR, and NBD, respectively. The experimental data support the theory that quenching takes place via a \"transfer-to-trap\" mechanism which proposes, firstly, that excitation energy is transferred between fluorophores and may reach a \"trap site,\" resulting in immediate energy dissipation, and, secondly, that trap sites are formed in a concentration-dependent manner. Some previous work suggested that quenching occurs only when fluorophores aggregate, or form long-lived dimers, but our data and this theory argue that traps may be \"statistical pairs\" of fluorophores that exist only transiently. Our findings should inspire future work to assess whether these traps can be charge-transfer states, excited-state dimers, or something else.</p>","PeriodicalId":8922,"journal":{"name":"Biophysical journal","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11427787/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysical journal","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.bpj.2024.07.026","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/22 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0

Abstract

It is important to understand the behaviors of fluorescent molecules because, firstly, they are often utilized as probes in biophysical experiments and, secondly, they are crucial cofactors in biological processes such as photosynthesis. A phenomenon called "fluorescence quenching" occurs when fluorophores are present at high concentrations, but the mechanisms for quenching are debated. Here, we used a technique called "in-membrane electrophoresis" to generate concentration gradients of fluorophores within a supported lipid bilayer, across which quenching was expected to occur. Fluorescence lifetime imaging microscopy (FLIM) provides images where the fluorescence intensity in each pixel is correlated to fluorescence lifetime: the intensity provides information about the location and concentration of fluorophores and the lifetime reveals the occurrence of energy-dissipative processes. FLIM was used to compare the quenching behavior of three commonly used fluorophores: Texas Red (TR), nitrobenzoaxadiazole (NBD), and 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY). FLIM images provided evidence of quenching in regions where the fluorophores accumulated, but the degree of quenching varied between the different fluorophores. The relationship between quenching and concentration was quantified and the "critical radius for trap formation," representing the relative quenching strength, was calculated as 2.70, 2.02, and 1.14 nm, for BODIPY, TR, and NBD, respectively. The experimental data support the theory that quenching takes place via a "transfer-to-trap" mechanism which proposes, firstly, that excitation energy is transferred between fluorophores and may reach a "trap site," resulting in immediate energy dissipation, and, secondly, that trap sites are formed in a concentration-dependent manner. Some previous work suggested that quenching occurs only when fluorophores aggregate, or form long-lived dimers, but our data and this theory argue that traps may be "statistical pairs" of fluorophores that exist only transiently. Our findings should inspire future work to assess whether these traps can be charge-transfer states, excited-state dimers, or something else.

脂质双分子层中荧光团浓度淬灭的转移到捕获机制的证据。
了解荧光分子的行为非常重要,首先,荧光分子经常被用作生物物理实验的探针;其次,荧光分子是光合作用等生物过程中的重要辅助因子。当荧光团高浓度存在时,会出现一种被称为 "荧光淬灭 "的现象,但关于淬灭的机制还存在争议。在这里,我们使用了一种名为 "膜内电泳 "的技术,在支撑脂质双分子层(SLB)内产生荧光团的浓度梯度,预计淬灭会在梯度上发生。荧光寿命成像显微镜(FLIM)可提供每个像素的荧光强度与荧光寿命相关的图像:荧光强度可提供有关荧光团位置和浓度的信息,荧光寿命可揭示能量耗散过程的发生。FLIM 用于比较三种常用荧光团的淬灭行为:德克萨斯红(TR)、硝基苯并噁二唑(NBD)和 4,4-二氟-4-硼-3a,4a-二氮杂-s-茚(BODIPY)。FLIM 图像显示,在荧光团聚集的区域存在淬灭现象,但不同荧光团的淬灭程度不同。对淬灭与浓度之间的关系进行了量化,并计算出 BODIPY、TR 和 NBD 的 "陷阱形成临界半径"(代表相对淬灭强度)分别为 2.70、2.02 和 1.14 nm。实验数据支持通过 "转移到陷阱 "机制进行淬灭的理论,该机制提出:首先,激发能量在荧光团之间转移,并可能到达 "陷阱位点",导致能量立即耗散;其次,陷阱位点的形成与浓度有关。以前的一些研究表明,只有当荧光团聚集或形成长寿命二聚体时才会发生淬灭,但我们的数据和这一理论认为,陷阱可能是荧光团的 "统计对",只短暂存在。我们的发现应能启发未来的工作,以评估这些陷阱是否可能是电荷转移态、激发态二聚体或其他。
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
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
×
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:481959085
Book学术官方微信