Spermine Binding to GC-Rich DNA: Experimental and Theoretical Studies
The DNA binding of spermine has been studied using experimental and computational approaches. Spermine blocks 5′-GC interstrand crosslinking by 2,5-diaziridinylbenzoquinone in the oligonucleotide duplex 5′-CTTCCAAGATGCATCAGATG 5′-CATCTGATGCATCTTGGAAG (where the underlined nucleotide bases represent...
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Veröffentlicht in: | Archives of biochemistry and biophysics 1996-01, Vol.325 (1), p.39-46 |
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creator | Yuki, Masayuki Grukhin, Vladislav Lee, Chong-Soon Haworth, Ian S. |
description | The DNA binding of spermine has been studied using experimental and computational approaches. Spermine blocks 5′-GC interstrand crosslinking by 2,5-diaziridinylbenzoquinone in the oligonucleotide duplex 5′-CTTCCAAGATGCATCAGATG 5′-CATCTGATGCATCTTGGAAG (where the underlined nucleotide bases represent the crosslinking site). Molecular dynamics simulations suggest that this is a result of preferential spermine binding at the 5′-GC major groove site of the oligonucleotide. A further simulation with a GC-alternating sequence shows a similar preference for the 5′-GC step. In a simulation including multiple spermine molecules, occupation of alternate 5′-GC steps occurred. From this, we deduce a mechanism for the experimentally observed cooperativity of spermine binding to poly(dGdC)2. |
doi_str_mv | 10.1006/abbi.1996.0005 |
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Spermine blocks 5′-GC interstrand crosslinking by 2,5-diaziridinylbenzoquinone in the oligonucleotide duplex 5′-CTTCCAAGATGCATCAGATG 5′-CATCTGATGCATCTTGGAAG (where the underlined nucleotide bases represent the crosslinking site). Molecular dynamics simulations suggest that this is a result of preferential spermine binding at the 5′-GC major groove site of the oligonucleotide. A further simulation with a GC-alternating sequence shows a similar preference for the 5′-GC step. In a simulation including multiple spermine molecules, occupation of alternate 5′-GC steps occurred. From this, we deduce a mechanism for the experimentally observed cooperativity of spermine binding to poly(dGdC)2.</description><identifier>ISSN: 0003-9861</identifier><identifier>EISSN: 1096-0384</identifier><identifier>DOI: 10.1006/abbi.1996.0005</identifier><identifier>PMID: 8554341</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aziridines - pharmacology ; Base Composition ; Base Sequence ; Binding Sites ; Chemical Phenomena ; Chemistry, Physical ; Computer Simulation ; Cross-Linking Reagents - pharmacology ; crosslink ; diaziridinylquinone ; DNA ; DNA - chemistry ; DNA - metabolism ; Hydroquinones - pharmacology ; Models, Molecular ; molecular dynamics ; Molecular Sequence Data ; Oligodeoxyribonucleotides - chemistry ; Oligodeoxyribonucleotides - metabolism ; spermine ; Spermine - metabolism ; Spermine - pharmacology</subject><ispartof>Archives of biochemistry and biophysics, 1996-01, Vol.325 (1), p.39-46</ispartof><rights>1996 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c339t-9294acd5507c68e0fddfddee6189227562846930855e69b1f38a1d800a50a3c23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/abbi.1996.0005$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8554341$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yuki, Masayuki</creatorcontrib><creatorcontrib>Grukhin, Vladislav</creatorcontrib><creatorcontrib>Lee, Chong-Soon</creatorcontrib><creatorcontrib>Haworth, Ian S.</creatorcontrib><title>Spermine Binding to GC-Rich DNA: Experimental and Theoretical Studies</title><title>Archives of biochemistry and biophysics</title><addtitle>Arch Biochem Biophys</addtitle><description>The DNA binding of spermine has been studied using experimental and computational approaches. Spermine blocks 5′-GC interstrand crosslinking by 2,5-diaziridinylbenzoquinone in the oligonucleotide duplex 5′-CTTCCAAGATGCATCAGATG 5′-CATCTGATGCATCTTGGAAG (where the underlined nucleotide bases represent the crosslinking site). Molecular dynamics simulations suggest that this is a result of preferential spermine binding at the 5′-GC major groove site of the oligonucleotide. A further simulation with a GC-alternating sequence shows a similar preference for the 5′-GC step. In a simulation including multiple spermine molecules, occupation of alternate 5′-GC steps occurred. From this, we deduce a mechanism for the experimentally observed cooperativity of spermine binding to poly(dGdC)2.</description><subject>Aziridines - pharmacology</subject><subject>Base Composition</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>Chemical Phenomena</subject><subject>Chemistry, Physical</subject><subject>Computer Simulation</subject><subject>Cross-Linking Reagents - pharmacology</subject><subject>crosslink</subject><subject>diaziridinylquinone</subject><subject>DNA</subject><subject>DNA - chemistry</subject><subject>DNA - metabolism</subject><subject>Hydroquinones - pharmacology</subject><subject>Models, Molecular</subject><subject>molecular dynamics</subject><subject>Molecular Sequence Data</subject><subject>Oligodeoxyribonucleotides - chemistry</subject><subject>Oligodeoxyribonucleotides - metabolism</subject><subject>spermine</subject><subject>Spermine - metabolism</subject><subject>Spermine - pharmacology</subject><issn>0003-9861</issn><issn>1096-0384</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFPwzAMhSMEGmNw5YbUE7cOp2nThNsYYyBNILFxjrLEY0FdO5IOwb8n1SZuSJYs289P9kfIJYUhBeA3erl0QyolHwJAcUT6FCRPgYn8mPRji6VScHpKzkL4AKA051mP9ERR5CynfTKZb9FvXI3Jnautq9-Ttkmm4_TVmXVy_zy6TSbfUeE2WLe6SnRtk8UaG4-tM7GetzvrMJyTk5WuAl4c8oC8PUwW48d09jJ9Go9mqWFMtqnMZK6NLQooDRcIK2tjIHIqZJaVBc9EziWDeB1yuaQrJjS1AkAXoJnJ2IBc7323vvncYWjVxgWDVaVrbHZBlaUsSyFYFA73QuObEDyu1Db-oP2PoqA6bqrjpjpuquMWF64OzrvlBu2f_AAqzsV-jvG9L4deBeOwNmidR9Mq27j_rH8BWs16GA</recordid><startdate>19960101</startdate><enddate>19960101</enddate><creator>Yuki, Masayuki</creator><creator>Grukhin, Vladislav</creator><creator>Lee, Chong-Soon</creator><creator>Haworth, Ian S.</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>19960101</creationdate><title>Spermine Binding to GC-Rich DNA: Experimental and Theoretical Studies</title><author>Yuki, Masayuki ; Grukhin, Vladislav ; Lee, Chong-Soon ; Haworth, Ian S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c339t-9294acd5507c68e0fddfddee6189227562846930855e69b1f38a1d800a50a3c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Aziridines - pharmacology</topic><topic>Base Composition</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>Chemical Phenomena</topic><topic>Chemistry, Physical</topic><topic>Computer Simulation</topic><topic>Cross-Linking Reagents - pharmacology</topic><topic>crosslink</topic><topic>diaziridinylquinone</topic><topic>DNA</topic><topic>DNA - chemistry</topic><topic>DNA - metabolism</topic><topic>Hydroquinones - pharmacology</topic><topic>Models, Molecular</topic><topic>molecular dynamics</topic><topic>Molecular Sequence Data</topic><topic>Oligodeoxyribonucleotides - chemistry</topic><topic>Oligodeoxyribonucleotides - metabolism</topic><topic>spermine</topic><topic>Spermine - metabolism</topic><topic>Spermine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yuki, Masayuki</creatorcontrib><creatorcontrib>Grukhin, Vladislav</creatorcontrib><creatorcontrib>Lee, Chong-Soon</creatorcontrib><creatorcontrib>Haworth, Ian S.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of biochemistry and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yuki, Masayuki</au><au>Grukhin, Vladislav</au><au>Lee, Chong-Soon</au><au>Haworth, Ian S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Spermine Binding to GC-Rich DNA: Experimental and Theoretical Studies</atitle><jtitle>Archives of biochemistry and biophysics</jtitle><addtitle>Arch Biochem Biophys</addtitle><date>1996-01-01</date><risdate>1996</risdate><volume>325</volume><issue>1</issue><spage>39</spage><epage>46</epage><pages>39-46</pages><issn>0003-9861</issn><eissn>1096-0384</eissn><abstract>The DNA binding of spermine has been studied using experimental and computational approaches. Spermine blocks 5′-GC interstrand crosslinking by 2,5-diaziridinylbenzoquinone in the oligonucleotide duplex 5′-CTTCCAAGATGCATCAGATG 5′-CATCTGATGCATCTTGGAAG (where the underlined nucleotide bases represent the crosslinking site). Molecular dynamics simulations suggest that this is a result of preferential spermine binding at the 5′-GC major groove site of the oligonucleotide. A further simulation with a GC-alternating sequence shows a similar preference for the 5′-GC step. In a simulation including multiple spermine molecules, occupation of alternate 5′-GC steps occurred. From this, we deduce a mechanism for the experimentally observed cooperativity of spermine binding to poly(dGdC)2.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>8554341</pmid><doi>10.1006/abbi.1996.0005</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Aziridines - pharmacology Base Composition Base Sequence Binding Sites Chemical Phenomena Chemistry, Physical Computer Simulation Cross-Linking Reagents - pharmacology crosslink diaziridinylquinone DNA DNA - chemistry DNA - metabolism Hydroquinones - pharmacology Models, Molecular molecular dynamics Molecular Sequence Data Oligodeoxyribonucleotides - chemistry Oligodeoxyribonucleotides - metabolism spermine Spermine - metabolism Spermine - pharmacology |
title | Spermine Binding to GC-Rich DNA: Experimental and Theoretical Studies |
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