Fluoride-Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension
Fluorescent 2′‐deoxynucleotides containing a protecting group at the 3′‐O‐position are reversible terminators that enable array‐based DNA sequencing‐by‐synthesis (SBS) approaches. Herein, we describe the synthesis and full characterisation of four reversible terminators bearing a 3′‐blocking moiety...
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Veröffentlicht in: | Chemistry : a European journal 2011-03, Vol.17 (10), p.2903-2915 |
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creator | Knapp, Diana C. Serva, Saulius D'Onofrio, Jennifer Keller, Angelika Lubys, Arvydas Kurg, Ants Remm, Maido Engels, Joachim W. |
description | Fluorescent 2′‐deoxynucleotides containing a protecting group at the 3′‐O‐position are reversible terminators that enable array‐based DNA sequencing‐by‐synthesis (SBS) approaches. Herein, we describe the synthesis and full characterisation of four reversible terminators bearing a 3′‐blocking moiety and a linker‐dye system that is removable under the same fluoride‐based treatment. Each nucleotide analogue has a different fluorophore attached to the base through a fluoride‐cleavable linker and a 2‐cyanoethyl moiety as the 3′‐blocking group, which can be removed by using a fluoride treatment as well. Furthermore, we identified a DNA polymerase, namely, RevertAid M‐MuLV reverse transcriptase, which can incorporate the four modified reversible terminators. The synthesised nucleotides and the optimised DNA polymerase were used on CodeLink slides spotted with hairpin oligonucleotides to demonstrate their potential in a cyclic reversible terminating approach.
Bright new things: A new set of fluorescently labelled reversible terminators has been synthesised (see picture). A polymerase able to incorporate these compounds was found, and the complete system of terminator–polymerase was successfully used in a cyclic reversible terminating approach on CodeLink slides spotted with oligonucleotide probes. |
doi_str_mv | 10.1002/chem.201001952 |
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Bright new things: A new set of fluorescently labelled reversible terminators has been synthesised (see picture). A polymerase able to incorporate these compounds was found, and the complete system of terminator–polymerase was successfully used in a cyclic reversible terminating approach on CodeLink slides spotted with oligonucleotide probes.</description><identifier>ISSN: 0947-6539</identifier><identifier>EISSN: 1521-3765</identifier><identifier>DOI: 10.1002/chem.201001952</identifier><identifier>PMID: 21294195</identifier><identifier>CODEN: CEUJED</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Chemical compounds ; Chemistry ; Deoxyribonucleic acid ; DNA ; DNA polymerase ; DNA Primers - metabolism ; Fluorescence ; Fluorescent Dyes - chemical synthesis ; Fluorescent Dyes - chemistry ; fluoride ions ; Fluorides ; Fluorides - chemistry ; Leukemia Virus, Murine - enzymology ; Molecular Structure ; Nucleotides ; Oligonucleotide Probes - chemical synthesis ; Oligonucleotide Probes - chemistry ; Oligonucleotides ; reverse transcriptase ; reversible terminators ; RNA-Directed DNA Polymerase - metabolism ; Stopping ; Synthesis</subject><ispartof>Chemistry : a European journal, 2011-03, Vol.17 (10), p.2903-2915</ispartof><rights>Copyright © 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5382-85abb47fd12da6823d4c2144b70468a1dd29aecbca9ebb657052a2df3831e6523</citedby><cites>FETCH-LOGICAL-c5382-85abb47fd12da6823d4c2144b70468a1dd29aecbca9ebb657052a2df3831e6523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchem.201001952$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchem.201001952$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21294195$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Knapp, Diana C.</creatorcontrib><creatorcontrib>Serva, Saulius</creatorcontrib><creatorcontrib>D'Onofrio, Jennifer</creatorcontrib><creatorcontrib>Keller, Angelika</creatorcontrib><creatorcontrib>Lubys, Arvydas</creatorcontrib><creatorcontrib>Kurg, Ants</creatorcontrib><creatorcontrib>Remm, Maido</creatorcontrib><creatorcontrib>Engels, Joachim W.</creatorcontrib><title>Fluoride-Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension</title><title>Chemistry : a European journal</title><addtitle>Chem. Eur. J</addtitle><description>Fluorescent 2′‐deoxynucleotides containing a protecting group at the 3′‐O‐position are reversible terminators that enable array‐based DNA sequencing‐by‐synthesis (SBS) approaches. Herein, we describe the synthesis and full characterisation of four reversible terminators bearing a 3′‐blocking moiety and a linker‐dye system that is removable under the same fluoride‐based treatment. Each nucleotide analogue has a different fluorophore attached to the base through a fluoride‐cleavable linker and a 2‐cyanoethyl moiety as the 3′‐blocking group, which can be removed by using a fluoride treatment as well. Furthermore, we identified a DNA polymerase, namely, RevertAid M‐MuLV reverse transcriptase, which can incorporate the four modified reversible terminators. The synthesised nucleotides and the optimised DNA polymerase were used on CodeLink slides spotted with hairpin oligonucleotides to demonstrate their potential in a cyclic reversible terminating approach.
Bright new things: A new set of fluorescently labelled reversible terminators has been synthesised (see picture). A polymerase able to incorporate these compounds was found, and the complete system of terminator–polymerase was successfully used in a cyclic reversible terminating approach on CodeLink slides spotted with oligonucleotide probes.</description><subject>Chemical compounds</subject><subject>Chemistry</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA polymerase</subject><subject>DNA Primers - metabolism</subject><subject>Fluorescence</subject><subject>Fluorescent Dyes - chemical synthesis</subject><subject>Fluorescent Dyes - chemistry</subject><subject>fluoride ions</subject><subject>Fluorides</subject><subject>Fluorides - chemistry</subject><subject>Leukemia Virus, Murine - enzymology</subject><subject>Molecular Structure</subject><subject>Nucleotides</subject><subject>Oligonucleotide Probes - chemical synthesis</subject><subject>Oligonucleotide Probes - chemistry</subject><subject>Oligonucleotides</subject><subject>reverse transcriptase</subject><subject>reversible terminators</subject><subject>RNA-Directed DNA Polymerase - metabolism</subject><subject>Stopping</subject><subject>Synthesis</subject><issn>0947-6539</issn><issn>1521-3765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1v1DAQxSMEotvClSOKxIEeyOKP2I45IKHVtkVavrft0XLiWdbFcYqdLN3_Hoctq8IBTh55fu9pZl6WPcFoihEiL5s1tFOCUo0lI_eyCWYEF1Rwdj-bIFmKgjMqD7LDGK8QQpJT-jA7IJjIMgkm2frEDV2wBoqZA73RtYMX-a8_iA343m3zha7BOTD5Z9hAiDYh-RJCa73uuxBf5V-2vl9DtDHX3uTnEXLr84_BthDy-U0PPtrOP8oerLSL8Pj2PcrOT-bL2Vmx-HD6dvZmUTSMVqSomK7rUqwMJkbzilBTNgSXZS1QySuNjSFSQ1M3WkJdcyYQI5qYFa0oBs4IPcpe73yvh7oFM-4QtFPXaRwdtqrTVv3Z8XatvnYbRTFGFR8Nnt8ahO77ALFXrU2ncE576IaoKka5qHiJE3n8TxILUSGKkRzRZ3-hV90QfDpEojjnKRnJEjXdUU3oYgyw2o-NkRrjVmPcah93Ejy9u-we_51vAuQO-GEdbP9jp2Zn83d3zYud1sYebvZaHb4pLqhg6vL9qUKfLsTyUgh1QX8CntbHUg</recordid><startdate>20110301</startdate><enddate>20110301</enddate><creator>Knapp, Diana C.</creator><creator>Serva, Saulius</creator><creator>D'Onofrio, Jennifer</creator><creator>Keller, Angelika</creator><creator>Lubys, Arvydas</creator><creator>Kurg, Ants</creator><creator>Remm, Maido</creator><creator>Engels, Joachim W.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20110301</creationdate><title>Fluoride-Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension</title><author>Knapp, Diana C. ; Serva, Saulius ; D'Onofrio, Jennifer ; Keller, Angelika ; Lubys, Arvydas ; Kurg, Ants ; Remm, Maido ; Engels, Joachim W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5382-85abb47fd12da6823d4c2144b70468a1dd29aecbca9ebb657052a2df3831e6523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Chemical compounds</topic><topic>Chemistry</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA polymerase</topic><topic>DNA Primers - metabolism</topic><topic>Fluorescence</topic><topic>Fluorescent Dyes - chemical synthesis</topic><topic>Fluorescent Dyes - chemistry</topic><topic>fluoride ions</topic><topic>Fluorides</topic><topic>Fluorides - chemistry</topic><topic>Leukemia Virus, Murine - enzymology</topic><topic>Molecular Structure</topic><topic>Nucleotides</topic><topic>Oligonucleotide Probes - chemical synthesis</topic><topic>Oligonucleotide Probes - chemistry</topic><topic>Oligonucleotides</topic><topic>reverse transcriptase</topic><topic>reversible terminators</topic><topic>RNA-Directed DNA Polymerase - metabolism</topic><topic>Stopping</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Knapp, Diana C.</creatorcontrib><creatorcontrib>Serva, Saulius</creatorcontrib><creatorcontrib>D'Onofrio, Jennifer</creatorcontrib><creatorcontrib>Keller, Angelika</creatorcontrib><creatorcontrib>Lubys, Arvydas</creatorcontrib><creatorcontrib>Kurg, Ants</creatorcontrib><creatorcontrib>Remm, Maido</creatorcontrib><creatorcontrib>Engels, Joachim W.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemistry : a European journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Knapp, Diana C.</au><au>Serva, Saulius</au><au>D'Onofrio, Jennifer</au><au>Keller, Angelika</au><au>Lubys, Arvydas</au><au>Kurg, Ants</au><au>Remm, Maido</au><au>Engels, Joachim W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluoride-Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension</atitle><jtitle>Chemistry : a European journal</jtitle><addtitle>Chem. Eur. J</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>17</volume><issue>10</issue><spage>2903</spage><epage>2915</epage><pages>2903-2915</pages><issn>0947-6539</issn><eissn>1521-3765</eissn><coden>CEUJED</coden><abstract>Fluorescent 2′‐deoxynucleotides containing a protecting group at the 3′‐O‐position are reversible terminators that enable array‐based DNA sequencing‐by‐synthesis (SBS) approaches. Herein, we describe the synthesis and full characterisation of four reversible terminators bearing a 3′‐blocking moiety and a linker‐dye system that is removable under the same fluoride‐based treatment. Each nucleotide analogue has a different fluorophore attached to the base through a fluoride‐cleavable linker and a 2‐cyanoethyl moiety as the 3′‐blocking group, which can be removed by using a fluoride treatment as well. Furthermore, we identified a DNA polymerase, namely, RevertAid M‐MuLV reverse transcriptase, which can incorporate the four modified reversible terminators. The synthesised nucleotides and the optimised DNA polymerase were used on CodeLink slides spotted with hairpin oligonucleotides to demonstrate their potential in a cyclic reversible terminating approach.
Bright new things: A new set of fluorescently labelled reversible terminators has been synthesised (see picture). A polymerase able to incorporate these compounds was found, and the complete system of terminator–polymerase was successfully used in a cyclic reversible terminating approach on CodeLink slides spotted with oligonucleotide probes.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>21294195</pmid><doi>10.1002/chem.201001952</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Chemical compounds Chemistry Deoxyribonucleic acid DNA DNA polymerase DNA Primers - metabolism Fluorescence Fluorescent Dyes - chemical synthesis Fluorescent Dyes - chemistry fluoride ions Fluorides Fluorides - chemistry Leukemia Virus, Murine - enzymology Molecular Structure Nucleotides Oligonucleotide Probes - chemical synthesis Oligonucleotide Probes - chemistry Oligonucleotides reverse transcriptase reversible terminators RNA-Directed DNA Polymerase - metabolism Stopping Synthesis |
title | Fluoride-Cleavable, Fluorescently Labelled Reversible Terminators: Synthesis and Use in Primer Extension |
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