Some properties of site-specific nickase BspD6I and the possibility of its use in hybridization analysis of DNA
A new method for hybridization analysis of nucleic acids is proposed on the basis of the ability of site-specific nickases to cleave only one DNA strand. The method is based on the use of a labeled oligonucleotide with the recognition site of the nickase hybridized with the target (DNA or RNA) at an...
Gespeichert in:
Veröffentlicht in: | Biochemistry (Moscow) 2002-04, Vol.67 (4), p.498-502 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 502 |
---|---|
container_issue | 4 |
container_start_page | 498 |
container_title | Biochemistry (Moscow) |
container_volume | 67 |
creator | Zheleznaya, L A Perevyazova, T A Zheleznyakova, E N Matvienko, N I |
description | A new method for hybridization analysis of nucleic acids is proposed on the basis of the ability of site-specific nickases to cleave only one DNA strand. The method is based on the use of a labeled oligonucleotide with the recognition site of the nickase hybridized with the target (DNA or RNA) at an optimal temperature of the enzyme (55 degrees C). The two shorter oligonucleotides formed after the cleavage with the nickase do not complex with the target. Thus, a multiple cleavage of the labeled oligonucleotide takes place on one target molecule. The cleavage of the nucleotide is recorded either by polyacrylamide gel electrophoresis (when a radioactive labeled oligonucleotide is used) or by fluorescence measurements (if the oligonucleotide has the structure of a molecular beacon). The new method was tested on nickase BspD6I and a radioactive oligonucleotide complementary to the polylinker region of the viral DNA strand in bacteriophage M13mp19. Unfortunately, nickase BspD6I does not cleave DNA in the RNA-DNA duplexes and therefore cannot be used for detection of RNA targets. |
doi_str_mv | 10.1023/A:1015250426726 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_754564333</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71664451</sourcerecordid><originalsourceid>FETCH-LOGICAL-c343t-1f41f3a7db1461287afc6f449e91c0f03339dc19492317cc3ef26e196d1bd1b33</originalsourceid><addsrcrecordid>eNqF0T1PwzAQBmALgaAUZjZkMcAU8NnOpWYrLR-VKhiAuXIcWzWkSYiTofx6DJSFASRLJ0vPvbqzCTkCdg6Mi4vxJTBIecokx4zjFhkAslEimGTbZMAYw4SrTO2R_RBe4pUzJXbJHoBSiJgOSP1Yryxt2rqxbedtoLWjwXc2CY013nlDK29edbD0KjRTnFFdFbRbxpY6BJ_70nfrzx7fBdpH5Su6XOetL_y77nxdRa_LdfBfwdP78QHZcboM9nBTh-T55vppcpfMH25nk_E8MUKKLgEnwQmdFTlIBD7KtDPopFRWgWGOCSFUYUBJxQVkxgjrOFpQWEAejxBDcvadG1d7623oFisfjC1LXdm6D4sslSnKGBPl6d8SEKVM4V_I46gpwijCk1_wpe7b-A4xjHPkI2QY0fEG9fnKFoum9Svdrhc_XyM-AJ8FjvA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>722628606</pqid></control><display><type>article</type><title>Some properties of site-specific nickase BspD6I and the possibility of its use in hybridization analysis of DNA</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Zheleznaya, L A ; Perevyazova, T A ; Zheleznyakova, E N ; Matvienko, N I</creator><creatorcontrib>Zheleznaya, L A ; Perevyazova, T A ; Zheleznyakova, E N ; Matvienko, N I</creatorcontrib><description>A new method for hybridization analysis of nucleic acids is proposed on the basis of the ability of site-specific nickases to cleave only one DNA strand. The method is based on the use of a labeled oligonucleotide with the recognition site of the nickase hybridized with the target (DNA or RNA) at an optimal temperature of the enzyme (55 degrees C). The two shorter oligonucleotides formed after the cleavage with the nickase do not complex with the target. Thus, a multiple cleavage of the labeled oligonucleotide takes place on one target molecule. The cleavage of the nucleotide is recorded either by polyacrylamide gel electrophoresis (when a radioactive labeled oligonucleotide is used) or by fluorescence measurements (if the oligonucleotide has the structure of a molecular beacon). The new method was tested on nickase BspD6I and a radioactive oligonucleotide complementary to the polylinker region of the viral DNA strand in bacteriophage M13mp19. Unfortunately, nickase BspD6I does not cleave DNA in the RNA-DNA duplexes and therefore cannot be used for detection of RNA targets.</description><identifier>ISSN: 0006-2979</identifier><identifier>EISSN: 1608-3040</identifier><identifier>DOI: 10.1023/A:1015250426726</identifier><identifier>PMID: 11996665</identifier><language>eng</language><publisher>United States: Springer Nature B.V</publisher><subject>Bacteriophages - chemistry ; Deoxyribonuclease I - chemistry ; Deoxyribonucleic acid ; DNA ; DNA - chemistry ; DNA, Viral - chemistry ; Electrophoresis ; Electrophoresis, Polyacrylamide Gel ; Enzymes ; Fluorescence ; Gels ; Hybridization ; Hydrolysis ; Nucleic Acid Heteroduplexes - chemistry ; Nucleic Acid Hybridization - methods ; Nucleic acids ; Radioactive materials ; RNA - chemistry ; Spectrometry, Fluorescence</subject><ispartof>Biochemistry (Moscow), 2002-04, Vol.67 (4), p.498-502</ispartof><rights>MAIK "Nauka/Interperiodica" 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-1f41f3a7db1461287afc6f449e91c0f03339dc19492317cc3ef26e196d1bd1b33</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11996665$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zheleznaya, L A</creatorcontrib><creatorcontrib>Perevyazova, T A</creatorcontrib><creatorcontrib>Zheleznyakova, E N</creatorcontrib><creatorcontrib>Matvienko, N I</creatorcontrib><title>Some properties of site-specific nickase BspD6I and the possibility of its use in hybridization analysis of DNA</title><title>Biochemistry (Moscow)</title><addtitle>Biochemistry (Mosc)</addtitle><description>A new method for hybridization analysis of nucleic acids is proposed on the basis of the ability of site-specific nickases to cleave only one DNA strand. The method is based on the use of a labeled oligonucleotide with the recognition site of the nickase hybridized with the target (DNA or RNA) at an optimal temperature of the enzyme (55 degrees C). The two shorter oligonucleotides formed after the cleavage with the nickase do not complex with the target. Thus, a multiple cleavage of the labeled oligonucleotide takes place on one target molecule. The cleavage of the nucleotide is recorded either by polyacrylamide gel electrophoresis (when a radioactive labeled oligonucleotide is used) or by fluorescence measurements (if the oligonucleotide has the structure of a molecular beacon). The new method was tested on nickase BspD6I and a radioactive oligonucleotide complementary to the polylinker region of the viral DNA strand in bacteriophage M13mp19. Unfortunately, nickase BspD6I does not cleave DNA in the RNA-DNA duplexes and therefore cannot be used for detection of RNA targets.</description><subject>Bacteriophages - chemistry</subject><subject>Deoxyribonuclease I - chemistry</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>DNA, Viral - chemistry</subject><subject>Electrophoresis</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Enzymes</subject><subject>Fluorescence</subject><subject>Gels</subject><subject>Hybridization</subject><subject>Hydrolysis</subject><subject>Nucleic Acid Heteroduplexes - chemistry</subject><subject>Nucleic Acid Hybridization - methods</subject><subject>Nucleic acids</subject><subject>Radioactive materials</subject><subject>RNA - chemistry</subject><subject>Spectrometry, Fluorescence</subject><issn>0006-2979</issn><issn>1608-3040</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0T1PwzAQBmALgaAUZjZkMcAU8NnOpWYrLR-VKhiAuXIcWzWkSYiTofx6DJSFASRLJ0vPvbqzCTkCdg6Mi4vxJTBIecokx4zjFhkAslEimGTbZMAYw4SrTO2R_RBe4pUzJXbJHoBSiJgOSP1Yryxt2rqxbedtoLWjwXc2CY013nlDK29edbD0KjRTnFFdFbRbxpY6BJ_70nfrzx7fBdpH5Su6XOetL_y77nxdRa_LdfBfwdP78QHZcboM9nBTh-T55vppcpfMH25nk_E8MUKKLgEnwQmdFTlIBD7KtDPopFRWgWGOCSFUYUBJxQVkxgjrOFpQWEAejxBDcvadG1d7623oFisfjC1LXdm6D4sslSnKGBPl6d8SEKVM4V_I46gpwijCk1_wpe7b-A4xjHPkI2QY0fEG9fnKFoum9Svdrhc_XyM-AJ8FjvA</recordid><startdate>20020401</startdate><enddate>20020401</enddate><creator>Zheleznaya, L A</creator><creator>Perevyazova, T A</creator><creator>Zheleznyakova, E N</creator><creator>Matvienko, N I</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QL</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20020401</creationdate><title>Some properties of site-specific nickase BspD6I and the possibility of its use in hybridization analysis of DNA</title><author>Zheleznaya, L A ; Perevyazova, T A ; Zheleznyakova, E N ; Matvienko, N I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-1f41f3a7db1461287afc6f449e91c0f03339dc19492317cc3ef26e196d1bd1b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Bacteriophages - chemistry</topic><topic>Deoxyribonuclease I - chemistry</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>DNA, Viral - chemistry</topic><topic>Electrophoresis</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Enzymes</topic><topic>Fluorescence</topic><topic>Gels</topic><topic>Hybridization</topic><topic>Hydrolysis</topic><topic>Nucleic Acid Heteroduplexes - chemistry</topic><topic>Nucleic Acid Hybridization - methods</topic><topic>Nucleic acids</topic><topic>Radioactive materials</topic><topic>RNA - chemistry</topic><topic>Spectrometry, Fluorescence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zheleznaya, L A</creatorcontrib><creatorcontrib>Perevyazova, T A</creatorcontrib><creatorcontrib>Zheleznyakova, E N</creatorcontrib><creatorcontrib>Matvienko, N I</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemistry (Moscow)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zheleznaya, L A</au><au>Perevyazova, T A</au><au>Zheleznyakova, E N</au><au>Matvienko, N I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Some properties of site-specific nickase BspD6I and the possibility of its use in hybridization analysis of DNA</atitle><jtitle>Biochemistry (Moscow)</jtitle><addtitle>Biochemistry (Mosc)</addtitle><date>2002-04-01</date><risdate>2002</risdate><volume>67</volume><issue>4</issue><spage>498</spage><epage>502</epage><pages>498-502</pages><issn>0006-2979</issn><eissn>1608-3040</eissn><abstract>A new method for hybridization analysis of nucleic acids is proposed on the basis of the ability of site-specific nickases to cleave only one DNA strand. The method is based on the use of a labeled oligonucleotide with the recognition site of the nickase hybridized with the target (DNA or RNA) at an optimal temperature of the enzyme (55 degrees C). The two shorter oligonucleotides formed after the cleavage with the nickase do not complex with the target. Thus, a multiple cleavage of the labeled oligonucleotide takes place on one target molecule. The cleavage of the nucleotide is recorded either by polyacrylamide gel electrophoresis (when a radioactive labeled oligonucleotide is used) or by fluorescence measurements (if the oligonucleotide has the structure of a molecular beacon). The new method was tested on nickase BspD6I and a radioactive oligonucleotide complementary to the polylinker region of the viral DNA strand in bacteriophage M13mp19. Unfortunately, nickase BspD6I does not cleave DNA in the RNA-DNA duplexes and therefore cannot be used for detection of RNA targets.</abstract><cop>United States</cop><pub>Springer Nature B.V</pub><pmid>11996665</pmid><doi>10.1023/A:1015250426726</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-2979 |
ispartof | Biochemistry (Moscow), 2002-04, Vol.67 (4), p.498-502 |
issn | 0006-2979 1608-3040 |
language | eng |
recordid | cdi_proquest_miscellaneous_754564333 |
source | MEDLINE; SpringerNature Journals |
subjects | Bacteriophages - chemistry Deoxyribonuclease I - chemistry Deoxyribonucleic acid DNA DNA - chemistry DNA, Viral - chemistry Electrophoresis Electrophoresis, Polyacrylamide Gel Enzymes Fluorescence Gels Hybridization Hydrolysis Nucleic Acid Heteroduplexes - chemistry Nucleic Acid Hybridization - methods Nucleic acids Radioactive materials RNA - chemistry Spectrometry, Fluorescence |
title | Some properties of site-specific nickase BspD6I and the possibility of its use in hybridization analysis of DNA |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-22T23%3A40%3A55IST&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=Some%20properties%20of%20site-specific%20nickase%20BspD6I%20and%20the%20possibility%20of%20its%20use%20in%20hybridization%20analysis%20of%20DNA&rft.jtitle=Biochemistry%20(Moscow)&rft.au=Zheleznaya,%20L%20A&rft.date=2002-04-01&rft.volume=67&rft.issue=4&rft.spage=498&rft.epage=502&rft.pages=498-502&rft.issn=0006-2979&rft.eissn=1608-3040&rft_id=info:doi/10.1023/A:1015250426726&rft_dat=%3Cproquest_pubme%3E71664451%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=722628606&rft_id=info:pmid/11996665&rfr_iscdi=true |