Loading…

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...

Full description

Saved in:
Bibliographic Details
Main Authors: Riedl, Jan, Pohl, Radek, Ernsting, Nikolaus P, Orság, Petr, Fojta, Miroslav, Hocek, Michal
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 286
container_issue 9
container_start_page 2797
container_title
container_volume 3
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
fullrecord <record><control><sourceid>rsc</sourceid><recordid>TN_cdi_rsc_primary_c2sc20404e</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>c2sc20404e</sourcerecordid><originalsourceid>FETCH-rsc_primary_c2sc20404e3</originalsourceid><addsrcrecordid>eNqFkUFv00AQhQ0qEhXthTvScAOpKU6cgNpb1KQiUlskyj0a767jQeud1c66kvn1HScRHJDAlx299_zNzG5RvJ2Wl9OyuvpkZmJm5bycu5fFqRbTyedFdXXyu56Vr4tzkZ-lflU1Xcy-nL74dYe1857CDriB0BvvWMg6AQwW2NOOD2Lei_UAwv4JM5s2cUcG5hPsKHBsc4ueOk1B43tOqnDSmhNI7u0wdlg9LCcxcXYUgEJ2CU0mDrL2zuTEQXHSx-hd50LGNGhI_-9wDMGH9ePmI-ATksfau2tYWkujgx4a2vXpOPMuYWzlAtwBuh8jK7njmjxlXaClJgOK4DDuXFOwx_XjooLM45gXYDiSElV9uP8OEkcY7hvInuws3C_vVhuV0A9yiObWaR9LDamtmEt4dA5W3zbX8PcjnRWvGvTizo_nm-Ld7frHzddJErONiTq9ge2fePV___2__G20TfUMovO2mw</addsrcrecordid><sourcetype>Enrichment Source</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><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><source>Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)</source><creator>Riedl, Jan ; Pohl, Radek ; Ernsting, Nikolaus P ; Orság, Petr ; Fojta, Miroslav ; Hocek, Michal</creator><creatorcontrib>Riedl, Jan ; Pohl, Radek ; Ernsting, Nikolaus P ; Orság, Petr ; Fojta, Miroslav ; Hocek, Michal</creatorcontrib><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><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>
fulltext fulltext
identifier ISSN: 2041-6520
ispartof
issn 2041-6520
2041-6539
language eng
recordid cdi_rsc_primary_c2sc20404e
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T13%3A55%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-rsc&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Labelling%20of%20nucleosides%20and%20oligonucleotides%20by%20solvatochromic%204-aminophthalimide%20fluorophore%20for%20studying%20DNA-protein%20interactionsElectronic%20supplementary%20information%20(ESI)%20available:%20Additional%20figures%20and%20graphs,%20electrophoretic%20mobility%20shift%20assay%20of%20binding%20of%20p53%20to%20DNA,%20copies%20of%20NMR%20spectra%20and%20selected%20MALDI%20analyses%20of%20the%20modified%20DNA.%20See%20DOI:%2010.1039/c2sc20404e&rft.au=Riedl,%20Jan&rft.date=2012-07-30&rft.volume=3&rft.issue=9&rft.spage=2797&rft.epage=286&rft.pages=2797-286&rft.issn=2041-6520&rft.eissn=2041-6539&rft_id=info:doi/10.1039/c2sc20404e&rft_dat=%3Crsc%3Ec2sc20404e%3C/rsc%3E%3Cgrp_id%3Ecdi_FETCH-rsc_primary_c2sc20404e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true