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Labelling of nucleosides and oligonucleotides by solvatochromic 4-aminophthalimide fluorophore for studying DNA-protein interactionsElectronic supplementary information (ESI) available: Additional figures and graphs, electrophoretic mobility shift assay of binding of p53 to DNA, copies of NMR spectra and selected MALDI analyses of the modified DNA. See DOI: 10.1039/c2sc20404e
Solvatochromic fluorescent 4-aminophthalimide ( API ) and 4-( N , N -dimethylamino)phthalimide ( DAPI ) were attached covalently to 2-deoxycytidine or -adenosine via a non-conjugated propargyl linker by Sonogashira cross-coupling reactions of N -propargylphthalimides with halogenated nucleosides. Th...
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creator | Riedl, Jan Pohl, Radek Ernsting, Nikolaus P Orság, Petr Fojta, Miroslav Hocek, Michal |
description | Solvatochromic fluorescent 4-aminophthalimide (
API
) and 4-(
N
,
N
-dimethylamino)phthalimide (
DAPI
) were attached covalently to 2-deoxycytidine or -adenosine
via
a non-conjugated propargyl linker by Sonogashira cross-coupling reactions of
N
-propargylphthalimides with halogenated nucleosides. The nucleosides were phosphorylated to triphosphates and enzymatically incorporated into oligonucleotides by DNA polymerases.
API
-labelled DNA was used for the detection of DNA protein interactions with either the sequence-specific p53 protein or a non-specific single strand binding (SSB) protein. Both proteins changed the polarity around the fluorophore and increased (2-3 fold) the intensity of
API
fluorescence.
Solvatochromic fluorescent labels based on aminophthalimide were attached to nucleosides and dNTPs and enzymatically incorporated to DNA for studying of interactions with proteins. |
doi_str_mv | 10.1039/c2sc20404e |
format | article |
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API
) and 4-(
N
,
N
-dimethylamino)phthalimide (
DAPI
) were attached covalently to 2-deoxycytidine or -adenosine
via
a non-conjugated propargyl linker by Sonogashira cross-coupling reactions of
N
-propargylphthalimides with halogenated nucleosides. The nucleosides were phosphorylated to triphosphates and enzymatically incorporated into oligonucleotides by DNA polymerases.
API
-labelled DNA was used for the detection of DNA protein interactions with either the sequence-specific p53 protein or a non-specific single strand binding (SSB) protein. Both proteins changed the polarity around the fluorophore and increased (2-3 fold) the intensity of
API
fluorescence.
Solvatochromic fluorescent labels based on aminophthalimide were attached to nucleosides and dNTPs and enzymatically incorporated to DNA for studying of interactions with proteins.</description><identifier>ISSN: 2041-6520</identifier><identifier>EISSN: 2041-6539</identifier><identifier>DOI: 10.1039/c2sc20404e</identifier><language>eng</language><creationdate>2012-07</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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></links><search><creatorcontrib>Riedl, Jan</creatorcontrib><creatorcontrib>Pohl, Radek</creatorcontrib><creatorcontrib>Ernsting, Nikolaus P</creatorcontrib><creatorcontrib>Orság, Petr</creatorcontrib><creatorcontrib>Fojta, Miroslav</creatorcontrib><creatorcontrib>Hocek, Michal</creatorcontrib><title>Labelling of nucleosides and oligonucleotides by solvatochromic 4-aminophthalimide fluorophore for studying DNA-protein interactionsElectronic supplementary information (ESI) available: Additional figures and graphs, electrophoretic mobility shift assay of binding of p53 to DNA, copies of NMR spectra and selected MALDI analyses of the modified DNA. See DOI: 10.1039/c2sc20404e</title><description>Solvatochromic fluorescent 4-aminophthalimide (
API
) and 4-(
N
,
N
-dimethylamino)phthalimide (
DAPI
) were attached covalently to 2-deoxycytidine or -adenosine
via
a non-conjugated propargyl linker by Sonogashira cross-coupling reactions of
N
-propargylphthalimides with halogenated nucleosides. The nucleosides were phosphorylated to triphosphates and enzymatically incorporated into oligonucleotides by DNA polymerases.
API
-labelled DNA was used for the detection of DNA protein interactions with either the sequence-specific p53 protein or a non-specific single strand binding (SSB) protein. Both proteins changed the polarity around the fluorophore and increased (2-3 fold) the intensity of
API
fluorescence.
Solvatochromic fluorescent labels based on aminophthalimide were attached to nucleosides and dNTPs and enzymatically incorporated to DNA for studying of interactions with proteins.</description><issn>2041-6520</issn><issn>2041-6539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkUFv00AQhQ0qEhXthTvScAOpKU6cgNpb1KQiUlskyj0a767jQeud1c66kvn1HScRHJDAlx299_zNzG5RvJ2Wl9OyuvpkZmJm5bycu5fFqRbTyedFdXXyu56Vr4tzkZ-lflU1Xcy-nL74dYe1857CDriB0BvvWMg6AQwW2NOOD2Lei_UAwv4JM5s2cUcG5hPsKHBsc4ueOk1B43tOqnDSmhNI7u0wdlg9LCcxcXYUgEJ2CU0mDrL2zuTEQXHSx-hd50LGNGhI_-9wDMGH9ePmI-ATksfau2tYWkujgx4a2vXpOPMuYWzlAtwBuh8jK7njmjxlXaClJgOK4DDuXFOwx_XjooLM45gXYDiSElV9uP8OEkcY7hvInuws3C_vVhuV0A9yiObWaR9LDamtmEt4dA5W3zbX8PcjnRWvGvTizo_nm-Ld7frHzddJErONiTq9ge2fePV___2__G20TfUMovO2mw</recordid><startdate>20120730</startdate><enddate>20120730</enddate><creator>Riedl, Jan</creator><creator>Pohl, Radek</creator><creator>Ernsting, Nikolaus P</creator><creator>Orság, Petr</creator><creator>Fojta, Miroslav</creator><creator>Hocek, Michal</creator><scope/></search><sort><creationdate>20120730</creationdate><title>Labelling of nucleosides and oligonucleotides by solvatochromic 4-aminophthalimide fluorophore for studying DNA-protein interactionsElectronic supplementary information (ESI) available: Additional figures and graphs, electrophoretic mobility shift assay of binding of p53 to DNA, copies of NMR spectra and selected MALDI analyses of the modified DNA. See DOI: 10.1039/c2sc20404e</title><author>Riedl, Jan ; Pohl, Radek ; Ernsting, Nikolaus P ; Orság, Petr ; Fojta, Miroslav ; Hocek, Michal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c2sc20404e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Riedl, Jan</creatorcontrib><creatorcontrib>Pohl, Radek</creatorcontrib><creatorcontrib>Ernsting, Nikolaus P</creatorcontrib><creatorcontrib>Orság, Petr</creatorcontrib><creatorcontrib>Fojta, Miroslav</creatorcontrib><creatorcontrib>Hocek, Michal</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Riedl, Jan</au><au>Pohl, Radek</au><au>Ernsting, Nikolaus P</au><au>Orság, Petr</au><au>Fojta, Miroslav</au><au>Hocek, Michal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Labelling of nucleosides and oligonucleotides by solvatochromic 4-aminophthalimide fluorophore for studying DNA-protein interactionsElectronic supplementary information (ESI) available: Additional figures and graphs, electrophoretic mobility shift assay of binding of p53 to DNA, copies of NMR spectra and selected MALDI analyses of the modified DNA. See DOI: 10.1039/c2sc20404e</atitle><date>2012-07-30</date><risdate>2012</risdate><volume>3</volume><issue>9</issue><spage>2797</spage><epage>286</epage><pages>2797-286</pages><issn>2041-6520</issn><eissn>2041-6539</eissn><abstract>Solvatochromic fluorescent 4-aminophthalimide (
API
) and 4-(
N
,
N
-dimethylamino)phthalimide (
DAPI
) were attached covalently to 2-deoxycytidine or -adenosine
via
a non-conjugated propargyl linker by Sonogashira cross-coupling reactions of
N
-propargylphthalimides with halogenated nucleosides. The nucleosides were phosphorylated to triphosphates and enzymatically incorporated into oligonucleotides by DNA polymerases.
API
-labelled DNA was used for the detection of DNA protein interactions with either the sequence-specific p53 protein or a non-specific single strand binding (SSB) protein. Both proteins changed the polarity around the fluorophore and increased (2-3 fold) the intensity of
API
fluorescence.
Solvatochromic fluorescent labels based on aminophthalimide were attached to nucleosides and dNTPs and enzymatically incorporated to DNA for studying of interactions with proteins.</abstract><doi>10.1039/c2sc20404e</doi><tpages>1</tpages></addata></record> |
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
title | Labelling of nucleosides and oligonucleotides by solvatochromic 4-aminophthalimide fluorophore for studying DNA-protein interactionsElectronic supplementary information (ESI) available: Additional figures and graphs, electrophoretic mobility shift assay of binding of p53 to DNA, copies of NMR spectra and selected MALDI analyses of the modified DNA. See DOI: 10.1039/c2sc20404e |
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