Fluorescent protein with environmentally-sensitive fluorescence lifetime for quantitative pH measurement

IF 3 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of biochemistry and biophysics Pub Date : 2025-04-01 Epub Date: 2025-02-18 DOI:10.1016/j.abb.2025.110350
Tatiana R. Simonyan , Elena A. Protasova , Anastasia V. Mamontova , Aleksander M. Shakhov , Daria V. Bodunova , Svetlana V. Sidorenko , Eugene G. Maksimov , Alexey M. Bogdanov
{"title":"Fluorescent protein with environmentally-sensitive fluorescence lifetime for quantitative pH measurement","authors":"Tatiana R. Simonyan ,&nbsp;Elena A. Protasova ,&nbsp;Anastasia V. Mamontova ,&nbsp;Aleksander M. Shakhov ,&nbsp;Daria V. Bodunova ,&nbsp;Svetlana V. Sidorenko ,&nbsp;Eugene G. Maksimov ,&nbsp;Alexey M. Bogdanov","doi":"10.1016/j.abb.2025.110350","DOIUrl":null,"url":null,"abstract":"<div><div>Intracellular pH is a key factor in cell homeostasis, regulated within specific compartments, and changes in pH can result from or affect biochemical pathways. This study explores a yellow fluorescent protein EYFP-G65T as a core for a time-resolved pH-indicator. Among the tested designs—a circular permutant, a chimeric SypHer3s-like construct, and an unmodified protein—the unmodified EYFP-G65T performed best for live-cell imaging. Upon two-photon excitation, purified EYFP-G65T exhibited a 4.5-fold increase in mean fluorescence lifetime across pH 5.5–7 and a 7-fold change in its major component's lifetime from pH 6.5–8. Using this indicator, we measured pH values ranging from 6 to 8 in various organelles, and mapped pH shifts in mitochondria and the Golgi apparatus in response to stimuli.</div></div>","PeriodicalId":8174,"journal":{"name":"Archives of biochemistry and biophysics","volume":"766 ","pages":"Article 110350"},"PeriodicalIF":3.0000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of biochemistry and biophysics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0003986125000633","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/18 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Intracellular pH is a key factor in cell homeostasis, regulated within specific compartments, and changes in pH can result from or affect biochemical pathways. This study explores a yellow fluorescent protein EYFP-G65T as a core for a time-resolved pH-indicator. Among the tested designs—a circular permutant, a chimeric SypHer3s-like construct, and an unmodified protein—the unmodified EYFP-G65T performed best for live-cell imaging. Upon two-photon excitation, purified EYFP-G65T exhibited a 4.5-fold increase in mean fluorescence lifetime across pH 5.5–7 and a 7-fold change in its major component's lifetime from pH 6.5–8. Using this indicator, we measured pH values ranging from 6 to 8 in various organelles, and mapped pH shifts in mitochondria and the Golgi apparatus in response to stimuli.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
具有环境敏感荧光寿命的荧光蛋白,用于定量pH测定
细胞内pH值是细胞内稳态的关键因素,在特定的区室内受到调节,pH值的变化可能是生化途径的结果或影响。本研究探索黄色荧光蛋白EYFP-G65T作为时间分辨ph指标的核心。在所测试的设计中——圆形排列体、嵌合的sypher3样结构和未修饰的蛋白质——未修饰的EYFP-G65T在活细胞成像方面表现最好。在双光子激发下,纯化的EYFP-G65T在pH值5.5-7范围内的平均荧光寿命增加了4.5倍,在pH值6.5-8范围内,其主要成分的寿命变化了7倍。利用这一指标,我们测量了各种细胞器的pH值,范围从6到8,并绘制了线粒体和高尔基体在刺激下的pH变化。
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 去求助
来源期刊
Archives of biochemistry and biophysics
Archives of biochemistry and biophysics 生物-生化与分子生物学
CiteScore
7.40
自引率
0.00%
发文量
245
审稿时长
26 days
期刊介绍: Archives of Biochemistry and Biophysics publishes quality original articles and reviews in the developing areas of biochemistry and biophysics. Research Areas Include: • Enzyme and protein structure, function, regulation. Folding, turnover, and post-translational processing • Biological oxidations, free radical reactions, redox signaling, oxygenases, P450 reactions • Signal transduction, receptors, membrane transport, intracellular signals. Cellular and integrated metabolism.
期刊最新文献
Structural analyses of oxygen channels of animal, soybean and manganese lipoxygenases The LINC00612/miR-331-3p/SOCS1 axis mediates the cardioprotective effect of sevoflurane against myocardial ischemia-reperfusion injury The strategic hyper-reactivity toward GSSG which avoids aggregation in the nascent lysozymes: from Cys94 in egg to Cys6 in humans Discovery and characterization of a covalent inhibitor of New Delhi metallo β-lactamase The regulatory subunit of acetohydroxyacid synthase enhances the catalysis of its catalytic subunit on 2-ketobutyrate
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1