Automated one-step DNA sequencing based on nanoliter reaction volumes and capillary electrophoresis

An integrated system with a nano-reactor for cycle-sequencing reaction coupled to on-line purification and capillary gel electrophoresis has been demonstrated. Fifty nanoliters of reagent solution, which includes dye-labeled terminators, polymerase, BSA and template, was aspirated and mixed with the...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nucleic acids research 2000-08, Vol.28 (15), p.E73-73
Hauptverfasser: Pang, H M, Yeung, E S
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 73
container_issue 15
container_start_page E73
container_title Nucleic acids research
container_volume 28
creator Pang, H M
Yeung, E S
description An integrated system with a nano-reactor for cycle-sequencing reaction coupled to on-line purification and capillary gel electrophoresis has been demonstrated. Fifty nanoliters of reagent solution, which includes dye-labeled terminators, polymerase, BSA and template, was aspirated and mixed with the template inside the nano-reactor followed by cycle-sequencing reaction. The reaction products were then purified by a size-exclusion chromatographic column operated at 50 degrees C followed by room temperature on-line injection of the DNA fragments into a capillary for gel electrophoresis. Over 450 bases of DNA can be separated and identified. As little as 25 nl reagent solution can be used for the cycle-sequencing reaction with a slightly shorter read length. Significant savings on reagent cost is achieved because the remaining stock solution can be reused without contamination. The steps of cycle sequencing, on-line purification, injection, DNA separation, capillary regeneration, gel-filling and fluidic manipulation were performed with complete automation. This system can be readily multiplexed for high-throughput DNA sequencing or PCR analysis directly from templates or even biological materials.
doi_str_mv 10.1093/nar/28.15.e73
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_102692</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>17621677</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3813-544876aea99a379a61e28ee0feb14c2ac16c131940ddc12035454cf5ad475ffe3</originalsourceid><addsrcrecordid>eNqFkr1vFDEQxS0EIiFQ0iJDQbcXj792t6A4hU8pIg3Uls87m3O0ay-2NxL_fUwuQgdNKlue3_P4PQ8hr4FtgPXiPNh0zrsNqA224gk5BaF5I3vNnx7tT8iLnG8YAwlKPicnVck6ofUpcdu1xNkWHGgM2OSCC_34fUsz_loxOB-u6c7m-yoNNsTJF0w0oXXF16PbOK0zZmrDQJ1d_DTZ9JvihK6kuOxjwuzzS_JstFPGVw_rGfn5-dOPi6_N5dWXbxfby8aJDkSjpOxabdH2vRVtbzUg7xDZiDuQjlsH2oGAXrJhcMCZUFJJNyo7yFaNI4oz8uFw77LuZhwchpLsZJbk5_oqE603_1aC35vreGuAcd3zqn970MdcvMmuWnV7F0OobkzHpAJVmfcPPVKsCeViZp8dVt8B45pNC1wxyeWjILSag27bCr77D7yJawo1KMMZU5p3uq9Qc4BcijknHP-6Amb-zIGpc2B4Z0CZOgeVf3McxRF9-HhxBxv8sEw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>200562869</pqid></control><display><type>article</type><title>Automated one-step DNA sequencing based on nanoliter reaction volumes and capillary electrophoresis</title><source>MEDLINE</source><source>Full-Text Journals in Chemistry (Open access)</source><source>Oxford University Press Open Access</source><source>PubMed Central</source><creator>Pang, H M ; Yeung, E S</creator><creatorcontrib>Pang, H M ; Yeung, E S ; Ames Laboratory (AMES), Ames, IA</creatorcontrib><description>An integrated system with a nano-reactor for cycle-sequencing reaction coupled to on-line purification and capillary gel electrophoresis has been demonstrated. Fifty nanoliters of reagent solution, which includes dye-labeled terminators, polymerase, BSA and template, was aspirated and mixed with the template inside the nano-reactor followed by cycle-sequencing reaction. The reaction products were then purified by a size-exclusion chromatographic column operated at 50 degrees C followed by room temperature on-line injection of the DNA fragments into a capillary for gel electrophoresis. Over 450 bases of DNA can be separated and identified. As little as 25 nl reagent solution can be used for the cycle-sequencing reaction with a slightly shorter read length. Significant savings on reagent cost is achieved because the remaining stock solution can be reused without contamination. The steps of cycle sequencing, on-line purification, injection, DNA separation, capillary regeneration, gel-filling and fluidic manipulation were performed with complete automation. This system can be readily multiplexed for high-throughput DNA sequencing or PCR analysis directly from templates or even biological materials.</description><identifier>ISSN: 1362-4962</identifier><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/28.15.e73</identifier><identifier>PMID: 10908366</identifier><identifier>CODEN: NARHAD</identifier><language>eng</language><publisher>England: Oxford Publishing Limited (England)</publisher><subject>AMES LABORATORY ; Automation ; BASIC BIOLOGICAL SCIENCES ; Chromatography, Gel - methods ; Costs and Cost Analysis ; DNA - isolation &amp; purification ; DNA SEQUENCING ; ELECTROPHORESIS ; Electrophoresis, Capillary ; NAR Methods Online ; Sequence Analysis, DNA - economics ; Sequence Analysis, DNA - instrumentation ; Sequence Analysis, DNA - methods</subject><ispartof>Nucleic acids research, 2000-08, Vol.28 (15), p.E73-73</ispartof><rights>Copyright Oxford University Press(England) Aug 1, 2000</rights><rights>Copyright © 2000 Oxford University Press 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3813-544876aea99a379a61e28ee0feb14c2ac16c131940ddc12035454cf5ad475ffe3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC102692/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC102692/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10908366$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/804515$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Pang, H M</creatorcontrib><creatorcontrib>Yeung, E S</creatorcontrib><creatorcontrib>Ames Laboratory (AMES), Ames, IA</creatorcontrib><title>Automated one-step DNA sequencing based on nanoliter reaction volumes and capillary electrophoresis</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>An integrated system with a nano-reactor for cycle-sequencing reaction coupled to on-line purification and capillary gel electrophoresis has been demonstrated. Fifty nanoliters of reagent solution, which includes dye-labeled terminators, polymerase, BSA and template, was aspirated and mixed with the template inside the nano-reactor followed by cycle-sequencing reaction. The reaction products were then purified by a size-exclusion chromatographic column operated at 50 degrees C followed by room temperature on-line injection of the DNA fragments into a capillary for gel electrophoresis. Over 450 bases of DNA can be separated and identified. As little as 25 nl reagent solution can be used for the cycle-sequencing reaction with a slightly shorter read length. Significant savings on reagent cost is achieved because the remaining stock solution can be reused without contamination. The steps of cycle sequencing, on-line purification, injection, DNA separation, capillary regeneration, gel-filling and fluidic manipulation were performed with complete automation. This system can be readily multiplexed for high-throughput DNA sequencing or PCR analysis directly from templates or even biological materials.</description><subject>AMES LABORATORY</subject><subject>Automation</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Chromatography, Gel - methods</subject><subject>Costs and Cost Analysis</subject><subject>DNA - isolation &amp; purification</subject><subject>DNA SEQUENCING</subject><subject>ELECTROPHORESIS</subject><subject>Electrophoresis, Capillary</subject><subject>NAR Methods Online</subject><subject>Sequence Analysis, DNA - economics</subject><subject>Sequence Analysis, DNA - instrumentation</subject><subject>Sequence Analysis, DNA - methods</subject><issn>1362-4962</issn><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkr1vFDEQxS0EIiFQ0iJDQbcXj792t6A4hU8pIg3Uls87m3O0ay-2NxL_fUwuQgdNKlue3_P4PQ8hr4FtgPXiPNh0zrsNqA224gk5BaF5I3vNnx7tT8iLnG8YAwlKPicnVck6ofUpcdu1xNkWHGgM2OSCC_34fUsz_loxOB-u6c7m-yoNNsTJF0w0oXXF16PbOK0zZmrDQJ1d_DTZ9JvihK6kuOxjwuzzS_JstFPGVw_rGfn5-dOPi6_N5dWXbxfby8aJDkSjpOxabdH2vRVtbzUg7xDZiDuQjlsH2oGAXrJhcMCZUFJJNyo7yFaNI4oz8uFw77LuZhwchpLsZJbk5_oqE603_1aC35vreGuAcd3zqn970MdcvMmuWnV7F0OobkzHpAJVmfcPPVKsCeViZp8dVt8B45pNC1wxyeWjILSag27bCr77D7yJawo1KMMZU5p3uq9Qc4BcijknHP-6Amb-zIGpc2B4Z0CZOgeVf3McxRF9-HhxBxv8sEw</recordid><startdate>20000801</startdate><enddate>20000801</enddate><creator>Pang, H M</creator><creator>Yeung, E S</creator><general>Oxford Publishing Limited (England)</general><general>Oxford University Press</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>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>OTOTI</scope><scope>5PM</scope></search><sort><creationdate>20000801</creationdate><title>Automated one-step DNA sequencing based on nanoliter reaction volumes and capillary electrophoresis</title><author>Pang, H M ; Yeung, E S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3813-544876aea99a379a61e28ee0feb14c2ac16c131940ddc12035454cf5ad475ffe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>AMES LABORATORY</topic><topic>Automation</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Chromatography, Gel - methods</topic><topic>Costs and Cost Analysis</topic><topic>DNA - isolation &amp; purification</topic><topic>DNA SEQUENCING</topic><topic>ELECTROPHORESIS</topic><topic>Electrophoresis, Capillary</topic><topic>NAR Methods Online</topic><topic>Sequence Analysis, DNA - economics</topic><topic>Sequence Analysis, DNA - instrumentation</topic><topic>Sequence Analysis, DNA - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pang, H M</creatorcontrib><creatorcontrib>Yeung, E S</creatorcontrib><creatorcontrib>Ames Laboratory (AMES), Ames, IA</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pang, H M</au><au>Yeung, E S</au><aucorp>Ames Laboratory (AMES), Ames, IA</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Automated one-step DNA sequencing based on nanoliter reaction volumes and capillary electrophoresis</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2000-08-01</date><risdate>2000</risdate><volume>28</volume><issue>15</issue><spage>E73</spage><epage>73</epage><pages>E73-73</pages><issn>1362-4962</issn><issn>0305-1048</issn><eissn>1362-4962</eissn><coden>NARHAD</coden><abstract>An integrated system with a nano-reactor for cycle-sequencing reaction coupled to on-line purification and capillary gel electrophoresis has been demonstrated. Fifty nanoliters of reagent solution, which includes dye-labeled terminators, polymerase, BSA and template, was aspirated and mixed with the template inside the nano-reactor followed by cycle-sequencing reaction. The reaction products were then purified by a size-exclusion chromatographic column operated at 50 degrees C followed by room temperature on-line injection of the DNA fragments into a capillary for gel electrophoresis. Over 450 bases of DNA can be separated and identified. As little as 25 nl reagent solution can be used for the cycle-sequencing reaction with a slightly shorter read length. Significant savings on reagent cost is achieved because the remaining stock solution can be reused without contamination. The steps of cycle sequencing, on-line purification, injection, DNA separation, capillary regeneration, gel-filling and fluidic manipulation were performed with complete automation. This system can be readily multiplexed for high-throughput DNA sequencing or PCR analysis directly from templates or even biological materials.</abstract><cop>England</cop><pub>Oxford Publishing Limited (England)</pub><pmid>10908366</pmid><doi>10.1093/nar/28.15.e73</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1362-4962
ispartof Nucleic acids research, 2000-08, Vol.28 (15), p.E73-73
issn 1362-4962
0305-1048
1362-4962
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_102692
source MEDLINE; Full-Text Journals in Chemistry (Open access); Oxford University Press Open Access; PubMed Central
subjects AMES LABORATORY
Automation
BASIC BIOLOGICAL SCIENCES
Chromatography, Gel - methods
Costs and Cost Analysis
DNA - isolation & purification
DNA SEQUENCING
ELECTROPHORESIS
Electrophoresis, Capillary
NAR Methods Online
Sequence Analysis, DNA - economics
Sequence Analysis, DNA - instrumentation
Sequence Analysis, DNA - methods
title Automated one-step DNA sequencing based on nanoliter reaction volumes and capillary electrophoresis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T15%3A31%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Automated%20one-step%20DNA%20sequencing%20based%20on%20nanoliter%20reaction%20volumes%20and%20capillary%20electrophoresis&rft.jtitle=Nucleic%20acids%20research&rft.au=Pang,%20H%20M&rft.aucorp=Ames%20Laboratory%20(AMES),%20Ames,%20IA&rft.date=2000-08-01&rft.volume=28&rft.issue=15&rft.spage=E73&rft.epage=73&rft.pages=E73-73&rft.issn=1362-4962&rft.eissn=1362-4962&rft.coden=NARHAD&rft_id=info:doi/10.1093/nar/28.15.e73&rft_dat=%3Cproquest_pubme%3E17621677%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=200562869&rft_id=info:pmid/10908366&rfr_iscdi=true