Single Molecular Multianalyte (Ca2+, Mg2+) Fluorescent Probe and Applications to Bioimaging

Intracellular signal transduction relies on spatial and temporal signal transmitter dynamics. To clarify the correlations of these transmitter molecules, multicolor-imaging has been widely used. However, in the case of applying multiple indicators in a cell, spectral overlap of the indicators preven...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the American Chemical Society 2005-08, Vol.127 (31), p.10798-10799
Hauptverfasser: Komatsu, Hirokazu, Miki, Takahiro, Citterio, Daniel, Kubota, Takeshi, Shindo, Yutaka, Kitamura, Yoshiichiro, Oka, Kotaro, Suzuki, Koji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10799
container_issue 31
container_start_page 10798
container_title Journal of the American Chemical Society
container_volume 127
creator Komatsu, Hirokazu
Miki, Takahiro
Citterio, Daniel
Kubota, Takeshi
Shindo, Yutaka
Kitamura, Yoshiichiro
Oka, Kotaro
Suzuki, Koji
description Intracellular signal transduction relies on spatial and temporal signal transmitter dynamics. To clarify the correlations of these transmitter molecules, multicolor-imaging has been widely used. However, in the case of applying multiple indicators in a cell, spectral overlap of the indicators prevents accurate quantitative analysis. Moreover, the invasive (toxic) effect, the localization, the metabolism, as well as photobleaching of these indicators complicate the situation. Here, we show that single-molecular multifluorescent probes can overcome these problems. While intracellular calcium plays a critical role as a signal transmitter and magnesium acts as a cofactor in many situations, the correlations between the two cations are now the main issue. We designed and synthesized a Ca2+−Mg2+ responsive multifluorescent probe, KCM-1. KCM-1 shows a spectral blue shift upon complexation to Ca2+ and a red shift to the presence of Mg2+. With data analyzed at different excitation wavelengths, the concentrations of Ca2+ and Mg2+ are simultaneously quantified. Furthermore, by using the AM-ester method, intracellular Ca2+ and Mg2+ concentrations are simultaneously imaged. Such a type of intracellular multiple analyte imaging by a single-molecular multifluorescent probe is successfully demonstrated for the first time.
doi_str_mv 10.1021/ja0528228
format Article
fullrecord <record><control><sourceid>acs_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1021_ja0528228</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c130982254</sourcerecordid><originalsourceid>FETCH-LOGICAL-a447t-d5760f7bc309e6632e7bb349c9029e6eff35aa5f2092dc4df6cad6c9fb23046a3</originalsourceid><addsrcrecordid>eNptkF1LwzAUhoMoOj8u_AOSG0HRaj7apL3U-QkbipsgeBFO02R0xnYkLei_N7Lhbrw6nHMeXl4ehA4puaCE0cs5kIzljOUbaEAzRpKMMrGJBoQQlshc8B20G8I8rinL6TbaoYJIQQUfoPdJ3cycwePWGd078Hjcu66GBtx3Z_DJENjZOR7P2NkpvnN9603Qpunws29Lg6Gp8NVi4WoNXd02AXctvq7b-hNmMXYfbVlwwRys5h56vbudDh-S0dP94_BqlECayi6pMimIlaXmpDBCcGZkWfK00AVh8WCs5RlAZhkpWKXTygoNldCFLRknqQC-h06Xudq3IXhj1cLHCv5bUaJ-Bak_QZE9WrKLvvw01ZpcGYnA8QqAoMFZD42uw5qTUWLOWeSSJVeHznz9_cF_KCG5zNT0eaJuXsR0-DYZqbd1Luig5m3vo-HwT8EfA-6HXg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Single Molecular Multianalyte (Ca2+, Mg2+) Fluorescent Probe and Applications to Bioimaging</title><source>MEDLINE</source><source>ACS Publications</source><creator>Komatsu, Hirokazu ; Miki, Takahiro ; Citterio, Daniel ; Kubota, Takeshi ; Shindo, Yutaka ; Kitamura, Yoshiichiro ; Oka, Kotaro ; Suzuki, Koji</creator><creatorcontrib>Komatsu, Hirokazu ; Miki, Takahiro ; Citterio, Daniel ; Kubota, Takeshi ; Shindo, Yutaka ; Kitamura, Yoshiichiro ; Oka, Kotaro ; Suzuki, Koji</creatorcontrib><description>Intracellular signal transduction relies on spatial and temporal signal transmitter dynamics. To clarify the correlations of these transmitter molecules, multicolor-imaging has been widely used. However, in the case of applying multiple indicators in a cell, spectral overlap of the indicators prevents accurate quantitative analysis. Moreover, the invasive (toxic) effect, the localization, the metabolism, as well as photobleaching of these indicators complicate the situation. Here, we show that single-molecular multifluorescent probes can overcome these problems. While intracellular calcium plays a critical role as a signal transmitter and magnesium acts as a cofactor in many situations, the correlations between the two cations are now the main issue. We designed and synthesized a Ca2+−Mg2+ responsive multifluorescent probe, KCM-1. KCM-1 shows a spectral blue shift upon complexation to Ca2+ and a red shift to the presence of Mg2+. With data analyzed at different excitation wavelengths, the concentrations of Ca2+ and Mg2+ are simultaneously quantified. Furthermore, by using the AM-ester method, intracellular Ca2+ and Mg2+ concentrations are simultaneously imaged. Such a type of intracellular multiple analyte imaging by a single-molecular multifluorescent probe is successfully demonstrated for the first time.</description><identifier>ISSN: 0002-7863</identifier><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/ja0528228</identifier><identifier>PMID: 16076163</identifier><identifier>CODEN: JACSAT</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Biological and medical sciences ; Biosensors ; Biotechnology ; Calcium - chemistry ; Fluorescent Dyes - chemistry ; Fundamental and applied biological sciences. Psychology ; Magnesium - chemistry ; Methods. Procedures. Technologies ; Various methods and equipments</subject><ispartof>Journal of the American Chemical Society, 2005-08, Vol.127 (31), p.10798-10799</ispartof><rights>Copyright © 2005 American Chemical Society</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a447t-d5760f7bc309e6632e7bb349c9029e6eff35aa5f2092dc4df6cad6c9fb23046a3</citedby><cites>FETCH-LOGICAL-a447t-d5760f7bc309e6632e7bb349c9029e6eff35aa5f2092dc4df6cad6c9fb23046a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ja0528228$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ja0528228$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=17004832$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16076163$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Komatsu, Hirokazu</creatorcontrib><creatorcontrib>Miki, Takahiro</creatorcontrib><creatorcontrib>Citterio, Daniel</creatorcontrib><creatorcontrib>Kubota, Takeshi</creatorcontrib><creatorcontrib>Shindo, Yutaka</creatorcontrib><creatorcontrib>Kitamura, Yoshiichiro</creatorcontrib><creatorcontrib>Oka, Kotaro</creatorcontrib><creatorcontrib>Suzuki, Koji</creatorcontrib><title>Single Molecular Multianalyte (Ca2+, Mg2+) Fluorescent Probe and Applications to Bioimaging</title><title>Journal of the American Chemical Society</title><addtitle>J. Am. Chem. Soc</addtitle><description>Intracellular signal transduction relies on spatial and temporal signal transmitter dynamics. To clarify the correlations of these transmitter molecules, multicolor-imaging has been widely used. However, in the case of applying multiple indicators in a cell, spectral overlap of the indicators prevents accurate quantitative analysis. Moreover, the invasive (toxic) effect, the localization, the metabolism, as well as photobleaching of these indicators complicate the situation. Here, we show that single-molecular multifluorescent probes can overcome these problems. While intracellular calcium plays a critical role as a signal transmitter and magnesium acts as a cofactor in many situations, the correlations between the two cations are now the main issue. We designed and synthesized a Ca2+−Mg2+ responsive multifluorescent probe, KCM-1. KCM-1 shows a spectral blue shift upon complexation to Ca2+ and a red shift to the presence of Mg2+. With data analyzed at different excitation wavelengths, the concentrations of Ca2+ and Mg2+ are simultaneously quantified. Furthermore, by using the AM-ester method, intracellular Ca2+ and Mg2+ concentrations are simultaneously imaged. Such a type of intracellular multiple analyte imaging by a single-molecular multifluorescent probe is successfully demonstrated for the first time.</description><subject>Biological and medical sciences</subject><subject>Biosensors</subject><subject>Biotechnology</subject><subject>Calcium - chemistry</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Magnesium - chemistry</subject><subject>Methods. Procedures. Technologies</subject><subject>Various methods and equipments</subject><issn>0002-7863</issn><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkF1LwzAUhoMoOj8u_AOSG0HRaj7apL3U-QkbipsgeBFO02R0xnYkLei_N7Lhbrw6nHMeXl4ehA4puaCE0cs5kIzljOUbaEAzRpKMMrGJBoQQlshc8B20G8I8rinL6TbaoYJIQQUfoPdJ3cycwePWGd078Hjcu66GBtx3Z_DJENjZOR7P2NkpvnN9603Qpunws29Lg6Gp8NVi4WoNXd02AXctvq7b-hNmMXYfbVlwwRys5h56vbudDh-S0dP94_BqlECayi6pMimIlaXmpDBCcGZkWfK00AVh8WCs5RlAZhkpWKXTygoNldCFLRknqQC-h06Xudq3IXhj1cLHCv5bUaJ-Bak_QZE9WrKLvvw01ZpcGYnA8QqAoMFZD42uw5qTUWLOWeSSJVeHznz9_cF_KCG5zNT0eaJuXsR0-DYZqbd1Luig5m3vo-HwT8EfA-6HXg</recordid><startdate>20050810</startdate><enddate>20050810</enddate><creator>Komatsu, Hirokazu</creator><creator>Miki, Takahiro</creator><creator>Citterio, Daniel</creator><creator>Kubota, Takeshi</creator><creator>Shindo, Yutaka</creator><creator>Kitamura, Yoshiichiro</creator><creator>Oka, Kotaro</creator><creator>Suzuki, Koji</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050810</creationdate><title>Single Molecular Multianalyte (Ca2+, Mg2+) Fluorescent Probe and Applications to Bioimaging</title><author>Komatsu, Hirokazu ; Miki, Takahiro ; Citterio, Daniel ; Kubota, Takeshi ; Shindo, Yutaka ; Kitamura, Yoshiichiro ; Oka, Kotaro ; Suzuki, Koji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a447t-d5760f7bc309e6632e7bb349c9029e6eff35aa5f2092dc4df6cad6c9fb23046a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biological and medical sciences</topic><topic>Biosensors</topic><topic>Biotechnology</topic><topic>Calcium - chemistry</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Magnesium - chemistry</topic><topic>Methods. Procedures. Technologies</topic><topic>Various methods and equipments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Komatsu, Hirokazu</creatorcontrib><creatorcontrib>Miki, Takahiro</creatorcontrib><creatorcontrib>Citterio, Daniel</creatorcontrib><creatorcontrib>Kubota, Takeshi</creatorcontrib><creatorcontrib>Shindo, Yutaka</creatorcontrib><creatorcontrib>Kitamura, Yoshiichiro</creatorcontrib><creatorcontrib>Oka, Kotaro</creatorcontrib><creatorcontrib>Suzuki, Koji</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Komatsu, Hirokazu</au><au>Miki, Takahiro</au><au>Citterio, Daniel</au><au>Kubota, Takeshi</au><au>Shindo, Yutaka</au><au>Kitamura, Yoshiichiro</au><au>Oka, Kotaro</au><au>Suzuki, Koji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single Molecular Multianalyte (Ca2+, Mg2+) Fluorescent Probe and Applications to Bioimaging</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J. Am. Chem. Soc</addtitle><date>2005-08-10</date><risdate>2005</risdate><volume>127</volume><issue>31</issue><spage>10798</spage><epage>10799</epage><pages>10798-10799</pages><issn>0002-7863</issn><eissn>1520-5126</eissn><coden>JACSAT</coden><abstract>Intracellular signal transduction relies on spatial and temporal signal transmitter dynamics. To clarify the correlations of these transmitter molecules, multicolor-imaging has been widely used. However, in the case of applying multiple indicators in a cell, spectral overlap of the indicators prevents accurate quantitative analysis. Moreover, the invasive (toxic) effect, the localization, the metabolism, as well as photobleaching of these indicators complicate the situation. Here, we show that single-molecular multifluorescent probes can overcome these problems. While intracellular calcium plays a critical role as a signal transmitter and magnesium acts as a cofactor in many situations, the correlations between the two cations are now the main issue. We designed and synthesized a Ca2+−Mg2+ responsive multifluorescent probe, KCM-1. KCM-1 shows a spectral blue shift upon complexation to Ca2+ and a red shift to the presence of Mg2+. With data analyzed at different excitation wavelengths, the concentrations of Ca2+ and Mg2+ are simultaneously quantified. Furthermore, by using the AM-ester method, intracellular Ca2+ and Mg2+ concentrations are simultaneously imaged. Such a type of intracellular multiple analyte imaging by a single-molecular multifluorescent probe is successfully demonstrated for the first time.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16076163</pmid><doi>10.1021/ja0528228</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0002-7863
ispartof Journal of the American Chemical Society, 2005-08, Vol.127 (31), p.10798-10799
issn 0002-7863
1520-5126
language eng
recordid cdi_crossref_primary_10_1021_ja0528228
source MEDLINE; ACS Publications
subjects Biological and medical sciences
Biosensors
Biotechnology
Calcium - chemistry
Fluorescent Dyes - chemistry
Fundamental and applied biological sciences. Psychology
Magnesium - chemistry
Methods. Procedures. Technologies
Various methods and equipments
title Single Molecular Multianalyte (Ca2+, Mg2+) Fluorescent Probe and Applications to Bioimaging
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T20%3A49%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Single%20Molecular%20Multianalyte%20(Ca2+,%20Mg2+)%20Fluorescent%20Probe%20and%20Applications%20to%20Bioimaging&rft.jtitle=Journal%20of%20the%20American%20Chemical%20Society&rft.au=Komatsu,%20Hirokazu&rft.date=2005-08-10&rft.volume=127&rft.issue=31&rft.spage=10798&rft.epage=10799&rft.pages=10798-10799&rft.issn=0002-7863&rft.eissn=1520-5126&rft.coden=JACSAT&rft_id=info:doi/10.1021/ja0528228&rft_dat=%3Cacs_cross%3Ec130982254%3C/acs_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/16076163&rfr_iscdi=true