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Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons
Carbocyanine dye diS-C 3 (3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emit...
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Published in: | Journal of fluorescence 2014-03, Vol.24 (2), p.541-547 |
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creator | Plášek, Jaromír Gášková, Dana |
description | Carbocyanine dye diS-C
3
(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval,
F
(580)/
F
(560) fluorescence emission ratio, wavelength of emission spectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C
3
(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). Here we show that data corresponding to the three latter spectral assessments of diS-C
3
(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments. On the other hand, experiments based on the effortless measurements of fluorescence intensities should be interpreted cautiously because controversial results can be obtained, depending on the particular choice of cell-to-dye concentration ratio and emission wavelength. |
doi_str_mv | 10.1007/s10895-013-1323-6 |
format | article |
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3
(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval,
F
(580)/
F
(560) fluorescence emission ratio, wavelength of emission spectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C
3
(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). Here we show that data corresponding to the three latter spectral assessments of diS-C
3
(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments. On the other hand, experiments based on the effortless measurements of fluorescence intensities should be interpreted cautiously because controversial results can be obtained, depending on the particular choice of cell-to-dye concentration ratio and emission wavelength.</description><identifier>ISSN: 1053-0509</identifier><identifier>EISSN: 1573-4994</identifier><identifier>DOI: 10.1007/s10895-013-1323-6</identifier><identifier>PMID: 24258003</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Analytical Chemistry ; Biochemistry ; Biological and Medical Physics ; Biomedical and Life Sciences ; Biomedicine ; Biophysics ; Biotechnology ; Carbocyanines - chemistry ; Fluorescent Dyes - chemistry ; Membrane Potentials ; Original Paper ; Saccharomyces cerevisiae - chemistry ; Spectrometry, Fluorescence - methods</subject><ispartof>Journal of fluorescence, 2014-03, Vol.24 (2), p.541-547</ispartof><rights>Springer Science+Business Media New York 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2596-8756cfe7679c93b027c4feaf346085388f3191488a9901abc4e0c6a1cba5d2dd3</citedby><cites>FETCH-LOGICAL-c2596-8756cfe7679c93b027c4feaf346085388f3191488a9901abc4e0c6a1cba5d2dd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24258003$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Plášek, Jaromír</creatorcontrib><creatorcontrib>Gášková, Dana</creatorcontrib><title>Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons</title><title>Journal of fluorescence</title><addtitle>J Fluoresc</addtitle><addtitle>J Fluoresc</addtitle><description>Carbocyanine dye diS-C
3
(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval,
F
(580)/
F
(560) fluorescence emission ratio, wavelength of emission spectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C
3
(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). Here we show that data corresponding to the three latter spectral assessments of diS-C
3
(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments. On the other hand, experiments based on the effortless measurements of fluorescence intensities should be interpreted cautiously because controversial results can be obtained, depending on the particular choice of cell-to-dye concentration ratio and emission wavelength.</description><subject>Analytical Chemistry</subject><subject>Biochemistry</subject><subject>Biological and Medical Physics</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Biophysics</subject><subject>Biotechnology</subject><subject>Carbocyanines - chemistry</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Membrane Potentials</subject><subject>Original Paper</subject><subject>Saccharomyces cerevisiae - chemistry</subject><subject>Spectrometry, Fluorescence - methods</subject><issn>1053-0509</issn><issn>1573-4994</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9UcFu1TAQtBCIlgcfwAX5WA6GdWzHNjcUUUBqRaW2B06W42x4qZI42MmB3-CLcfQKR067K83M7s4Q8prDOw6g32cOxioGXDAuKsHqJ-ScKy2YtFY-LT0owUCBPSMvcn4AAGukeU7OKlkpAyDOye8mTsuIE86rT7_oNa7H2GUae3qTYsCch_kH7YZb1ogL8ZZejltMmAPOAentgmFNnt5n7GgfE72O87DGtFPWI9Kb0efJF82pTX4uc1zLmsGPu_x39Hn9QO-OOKR9V6Z-7mgT5_ySPOv9mPHVYz2Q-8tPd80XdvXt89fm4xULlbI1M1rVoUddaxusaKHSQfboeyFrMEoY0wtuuTTGWwvct0EihNrz0HrVVV0nDuTipLuk-HPDvLppKJ-NY7k1btlxrbU0VhR7D4SfoKEcmhP2bknDVAxzHNwehTtF4QrW7VG4unDePMpv7YTdP8Zf7wugOgHysluGyT3ELc3l5f-o_gHnCZRi</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Plášek, Jaromír</creator><creator>Gášková, Dana</creator><general>Springer US</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20140301</creationdate><title>Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons</title><author>Plášek, Jaromír ; Gášková, Dana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2596-8756cfe7679c93b027c4feaf346085388f3191488a9901abc4e0c6a1cba5d2dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Analytical Chemistry</topic><topic>Biochemistry</topic><topic>Biological and Medical Physics</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Biophysics</topic><topic>Biotechnology</topic><topic>Carbocyanines - chemistry</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Membrane Potentials</topic><topic>Original Paper</topic><topic>Saccharomyces cerevisiae - chemistry</topic><topic>Spectrometry, Fluorescence - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Plášek, Jaromír</creatorcontrib><creatorcontrib>Gášková, Dana</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of fluorescence</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Plášek, Jaromír</au><au>Gášková, Dana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons</atitle><jtitle>Journal of fluorescence</jtitle><stitle>J Fluoresc</stitle><addtitle>J Fluoresc</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>24</volume><issue>2</issue><spage>541</spage><epage>547</epage><pages>541-547</pages><issn>1053-0509</issn><eissn>1573-4994</eissn><abstract>Carbocyanine dye diS-C
3
(3) was repeatedly employed in monitoring the plasma membrane potential of yeast and other living cells. Four methods of measuring and evaluating probe fluorescence signal were used in different studies, based on following fluorescence parameters: fluorescence intensity emitted within a certain spectral interval,
F
(580)/
F
(560) fluorescence emission ratio, wavelength of emission spectrum maximum, and the ratio of respective fluorescence intensities corresponding to the diS-C
3
(3) bound to cytosolic macromolecules and remaining dissolved in the aqueous cell medium (i.e., unbound, or free). Here we show that data corresponding to the three latter spectral assessments of diS-C
3
(3) accumulation in cells is mutually convertible, which means that their alternative use cannot lead to ambiguities in the interpretation of the results of biological experiments. On the other hand, experiments based on the effortless measurements of fluorescence intensities should be interpreted cautiously because controversial results can be obtained, depending on the particular choice of cell-to-dye concentration ratio and emission wavelength.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>24258003</pmid><doi>10.1007/s10895-013-1323-6</doi><tpages>7</tpages></addata></record> |
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subjects | Analytical Chemistry Biochemistry Biological and Medical Physics Biomedical and Life Sciences Biomedicine Biophysics Biotechnology Carbocyanines - chemistry Fluorescent Dyes - chemistry Membrane Potentials Original Paper Saccharomyces cerevisiae - chemistry Spectrometry, Fluorescence - methods |
title | Complementary Methods of Processing diS-C3(3) Fluorescence Spectra Used for Monitoring the Plasma Membrane Potential of Yeast: Their Pros and Cons |
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