Mae E. James , Christiane Reick , Maryam Mohammad Qaed , Georgia A. Ceeney , Kornelija Rimgailaite , Robert G. Blore , Zofia X. Majewska , Douha Ghrieb , Andrea E. Gallio , Noa A. Marson , Jaswir Basran , Ezio Rosato , Charalambos P. Kyriacou , Emma L. Raven , Andrew J. Hudson
{"title":"基因编码血红素传感器的多光子荧光寿命成像","authors":"Mae E. James , Christiane Reick , Maryam Mohammad Qaed , Georgia A. Ceeney , Kornelija Rimgailaite , Robert G. Blore , Zofia X. Majewska , Douha Ghrieb , Andrea E. Gallio , Noa A. Marson , Jaswir Basran , Ezio Rosato , Charalambos P. Kyriacou , Emma L. Raven , Andrew J. Hudson","doi":"10.1016/j.jinorgbio.2025.113082","DOIUrl":null,"url":null,"abstract":"<div><div>Genetically-encoded fluorescence-based sensors have emerged as an essential tool for measuring the abundance of heme, revealing its trafficking pathways, and probing its signalling and regulatory role in cells. A number of different sensor designs have been described in the literature, and these typically report on the abundance of exchangeable heme <em>via</em> an intensity modulation of the emission from fluorescent-protein reporters. Here, we show that multi-photon fluorescence-lifetime imaging microscopy (MP-FLIM) can be used to monitor the response of heme sensors in transfected-HEK293 cells. The adoption of a multi-photon approach could extend heme quantification further to deep-tissue imaging in the future, where it could also reduce phototoxicity as the non-linear excitation of fluorescent reporters is confined to the focal volume.</div></div>","PeriodicalId":364,"journal":{"name":"Journal of Inorganic Biochemistry","volume":"274 ","pages":"Article 113082"},"PeriodicalIF":3.2000,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multi-photon fluorescence-lifetime imaging of a genetically-encoded heme sensor\",\"authors\":\"Mae E. James , Christiane Reick , Maryam Mohammad Qaed , Georgia A. Ceeney , Kornelija Rimgailaite , Robert G. Blore , Zofia X. Majewska , Douha Ghrieb , Andrea E. Gallio , Noa A. Marson , Jaswir Basran , Ezio Rosato , Charalambos P. Kyriacou , Emma L. Raven , Andrew J. Hudson\",\"doi\":\"10.1016/j.jinorgbio.2025.113082\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Genetically-encoded fluorescence-based sensors have emerged as an essential tool for measuring the abundance of heme, revealing its trafficking pathways, and probing its signalling and regulatory role in cells. A number of different sensor designs have been described in the literature, and these typically report on the abundance of exchangeable heme <em>via</em> an intensity modulation of the emission from fluorescent-protein reporters. Here, we show that multi-photon fluorescence-lifetime imaging microscopy (MP-FLIM) can be used to monitor the response of heme sensors in transfected-HEK293 cells. The adoption of a multi-photon approach could extend heme quantification further to deep-tissue imaging in the future, where it could also reduce phototoxicity as the non-linear excitation of fluorescent reporters is confined to the focal volume.</div></div>\",\"PeriodicalId\":364,\"journal\":{\"name\":\"Journal of Inorganic Biochemistry\",\"volume\":\"274 \",\"pages\":\"Article 113082\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Inorganic Biochemistry\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0162013425002624\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Inorganic Biochemistry","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0162013425002624","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Multi-photon fluorescence-lifetime imaging of a genetically-encoded heme sensor
Genetically-encoded fluorescence-based sensors have emerged as an essential tool for measuring the abundance of heme, revealing its trafficking pathways, and probing its signalling and regulatory role in cells. A number of different sensor designs have been described in the literature, and these typically report on the abundance of exchangeable heme via an intensity modulation of the emission from fluorescent-protein reporters. Here, we show that multi-photon fluorescence-lifetime imaging microscopy (MP-FLIM) can be used to monitor the response of heme sensors in transfected-HEK293 cells. The adoption of a multi-photon approach could extend heme quantification further to deep-tissue imaging in the future, where it could also reduce phototoxicity as the non-linear excitation of fluorescent reporters is confined to the focal volume.
期刊介绍:
The Journal of Inorganic Biochemistry is an established international forum for research in all aspects of Biological Inorganic Chemistry. Original papers of a high scientific level are published in the form of Articles (full length papers), Short Communications, Focused Reviews and Bioinorganic Methods. Topics include: the chemistry, structure and function of metalloenzymes; the interaction of inorganic ions and molecules with proteins and nucleic acids; the synthesis and properties of coordination complexes of biological interest including both structural and functional model systems; the function of metal- containing systems in the regulation of gene expression; the role of metals in medicine; the application of spectroscopic methods to determine the structure of metallobiomolecules; the preparation and characterization of metal-based biomaterials; and related systems. The emphasis of the Journal is on the structure and mechanism of action of metallobiomolecules.