Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery

Discovering new fluorochromes is significantly advanced by high-throughput screening (HTS) methods. In the present study a combination of small molecule microarray (SMM) prescreening and confocal laser scanning microscopy (CLSM) was developed in order to discover novel cell staining fluorescent dyes...

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Main Authors: Attila Bokros, Ágnes Medgyesi, Ferhan Ayaydin, László G. Puskás, Gabriella Fábián, Liliána Z. Fehér, Pradeep Kumar Reddy Cingaram, Bhavyashree Suresh, Begüm Peksel, Soujanya Kuntam, Eszter Molnár
Format: Article
Language:English
Published: MDPI AG 2013-08-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/18/8/9999
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spelling doaj-5d1fc615072e462f9a926328b9c833272020-11-24T21:35:51ZengMDPI AGMolecules1420-30492013-08-0118899991001310.3390/molecules18089999Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye DiscoveryAttila BokrosÁgnes MedgyesiFerhan AyaydinLászló G. PuskásGabriella FábiánLiliána Z. FehérPradeep Kumar Reddy CingaramBhavyashree SureshBegüm PekselSoujanya KuntamEszter MolnárDiscovering new fluorochromes is significantly advanced by high-throughput screening (HTS) methods. In the present study a combination of small molecule microarray (SMM) prescreening and confocal laser scanning microscopy (CLSM) was developed in order to discover novel cell staining fluorescent dyes. Compounds with high native fluorescence were selected from a 14,585-member library and further tested on living cells under the microscope. Eleven compartment-specific, cell-permeable (or plasma membrane-targeted) fluorochromes were identified. Their cytotoxicity was tested and found that between 1–10 micromolar range, they were non-toxic even during long-term incubations.http://www.mdpi.com/1420-3049/18/8/9999fluorescent dye discoveryhigh-throughput screeningsmall molecule microarrayconfocal laser scanning microscopy
collection DOAJ
language English
format Article
sources DOAJ
author Attila Bokros
Ágnes Medgyesi
Ferhan Ayaydin
László G. Puskás
Gabriella Fábián
Liliána Z. Fehér
Pradeep Kumar Reddy Cingaram
Bhavyashree Suresh
Begüm Peksel
Soujanya Kuntam
Eszter Molnár
spellingShingle Attila Bokros
Ágnes Medgyesi
Ferhan Ayaydin
László G. Puskás
Gabriella Fábián
Liliána Z. Fehér
Pradeep Kumar Reddy Cingaram
Bhavyashree Suresh
Begüm Peksel
Soujanya Kuntam
Eszter Molnár
Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery
Molecules
fluorescent dye discovery
high-throughput screening
small molecule microarray
confocal laser scanning microscopy
author_facet Attila Bokros
Ágnes Medgyesi
Ferhan Ayaydin
László G. Puskás
Gabriella Fábián
Liliána Z. Fehér
Pradeep Kumar Reddy Cingaram
Bhavyashree Suresh
Begüm Peksel
Soujanya Kuntam
Eszter Molnár
author_sort Attila Bokros
title Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery
title_short Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery
title_full Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery
title_fullStr Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery
title_full_unstemmed Combination of Small Molecule Microarray and Confocal Microscopy Techniques for Live Cell Staining Fluorescent Dye Discovery
title_sort combination of small molecule microarray and confocal microscopy techniques for live cell staining fluorescent dye discovery
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2013-08-01
description Discovering new fluorochromes is significantly advanced by high-throughput screening (HTS) methods. In the present study a combination of small molecule microarray (SMM) prescreening and confocal laser scanning microscopy (CLSM) was developed in order to discover novel cell staining fluorescent dyes. Compounds with high native fluorescence were selected from a 14,585-member library and further tested on living cells under the microscope. Eleven compartment-specific, cell-permeable (or plasma membrane-targeted) fluorochromes were identified. Their cytotoxicity was tested and found that between 1–10 micromolar range, they were non-toxic even during long-term incubations.
topic fluorescent dye discovery
high-throughput screening
small molecule microarray
confocal laser scanning microscopy
url http://www.mdpi.com/1420-3049/18/8/9999
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