Palladium(II)-coproporphyrin I as a photoactivable group in sequence-specific modification of nucleic acids by oligonucleotide derivatives
The 34-mer oligodeoxynucleotide was shown to be selectively modified at the G17 position upon photoirradiation in the presence of complementary 17-mer oligodeoxynucleotide bearing Pd(II)-coproporphyrin I covalently linked to the 5'-end phosphate group.
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| Veröffentlicht in: | FEBS letters 1990, Vol.259 (2), p.335-337 |
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| container_end_page | 337 |
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| container_issue | 2 |
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| container_title | FEBS letters |
| container_volume | 259 |
| creator | Fedorova, O.S. Savitskii, A.P. Shoikhet, K.G. Ponomarev, G.V. |
| description | The 34-mer oligodeoxynucleotide was shown to be selectively modified at the G17 position upon photoirradiation in the presence of complementary 17-mer oligodeoxynucleotide bearing Pd(II)-coproporphyrin I covalently linked to the 5'-end phosphate group. |
| doi_str_mv | 10.1016/0014-5793(90)80041-G |
| format | Article |
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Psychology ; Molecular Sequence Data ; Nucleic acids ; Nucleic bases, nucleotides ; Oligodeoxyribonucleotides - chemical synthesis ; Palladium ; Pd(II)-coproporphyrin I ; Phosphorus Radioisotopes ; Photochemistry ; Photoirradiation ; Por (COOH)4, palladium (II)-coproporphyrin I ; Porphyrins ; Sequence-specific modification</subject><ispartof>FEBS letters, 1990, Vol.259 (2), p.335-337</ispartof><rights>1990</rights><rights>FEBS Letters 259 (1990) 1873-3468 © 2015 Federation of European Biochemical Societies</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c495G-25d97be433e57882c09468449a1aecd199c6cda19a77cbd94332079cbff8aa23</citedby><cites>FETCH-LOGICAL-c495G-25d97be433e57882c09468449a1aecd199c6cda19a77cbd94332079cbff8aa23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0014-5793(90)80041-G$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,4009,27902,27903,27904,45974</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6767056$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2294023$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fedorova, O.S.</creatorcontrib><creatorcontrib>Savitskii, A.P.</creatorcontrib><creatorcontrib>Shoikhet, K.G.</creatorcontrib><creatorcontrib>Ponomarev, G.V.</creatorcontrib><title>Palladium(II)-coproporphyrin I as a photoactivable group in sequence-specific modification of nucleic acids by oligonucleotide derivatives</title><title>FEBS letters</title><addtitle>FEBS Lett</addtitle><description>The 34-mer oligodeoxynucleotide was shown to be selectively modified at the G17 position upon photoirradiation in the presence of complementary 17-mer oligodeoxynucleotide bearing Pd(II)-coproporphyrin I covalently linked to the 5'-end phosphate group.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Autoradiography</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>CMC, N-cyclohexyl-N'-morpholinoethyl carbodiimide metho-p-toluenesulfonate</subject><subject>Coproporphyrins</subject><subject>DMAP, 4-dimethylaminopyridine</subject><subject>DMF, dimethylformamide</subject><subject>DMSO, dimethylsulfoxide</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Molecular Sequence Data</subject><subject>Nucleic acids</subject><subject>Nucleic bases, nucleotides</subject><subject>Oligodeoxyribonucleotides - chemical synthesis</subject><subject>Palladium</subject><subject>Pd(II)-coproporphyrin I</subject><subject>Phosphorus Radioisotopes</subject><subject>Photochemistry</subject><subject>Photoirradiation</subject><subject>Por (COOH)4, palladium (II)-coproporphyrin I</subject><subject>Porphyrins</subject><subject>Sequence-specific modification</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUcFu1DAQtRCoLG3_ACQfEGoPKXbixPEFCaruslKlcujdcsaT1iiJg50U7S_w1Ti7qz0iTiO_9-Z55g0h7zm74YxXnxnjIiulKq4Uu64ZEzzbvCIrXssiK0RVvyark-QteRfjT5beNVdn5CzPlWB5sSJ_fpiuM9bN_dV2e52BH4MffRifd8ENdEtNpIaOz37yBib3YpoO6VPw80gTHfHXjANgFkcE1zqgvbdLNZPzA_UtHWboMOEGnI202VHfuSe_R_3kLFKLIbkmZ4wX5E1ruoiXx3pOHtd3j7ffs_uHzfb2630GQpWbLC-tkg2KosBS1nUOTKVlhVCGGwTLlYIKrOHKSAmNVUmYM6mgadvamLw4J58OtmnTNH6cdO8iYEphQD9HLVVZiCIXSSgOQgg-xoCtHoPrTdhpzvRyAb3Eq5d4tWJ6fwG9SW0fjv5z06M9NR0jT_zHI28imK4NZgAXT7JKVpKVVZKtD7LfrsPdf32t13ff8oVYcMX26DLPl4MRpkxfHAYdwS1Xsy4gTNp69--F_gJ5y7gU</recordid><startdate>1990</startdate><enddate>1990</enddate><creator>Fedorova, O.S.</creator><creator>Savitskii, A.P.</creator><creator>Shoikhet, K.G.</creator><creator>Ponomarev, G.V.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</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>7X8</scope></search><sort><creationdate>1990</creationdate><title>Palladium(II)-coproporphyrin I as a photoactivable group in sequence-specific modification of nucleic acids by oligonucleotide derivatives</title><author>Fedorova, O.S. ; Savitskii, A.P. ; Shoikhet, K.G. ; Ponomarev, G.V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c495G-25d97be433e57882c09468449a1aecd199c6cda19a77cbd94332079cbff8aa23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Autoradiography</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>CMC, N-cyclohexyl-N'-morpholinoethyl carbodiimide metho-p-toluenesulfonate</topic><topic>Coproporphyrins</topic><topic>DMAP, 4-dimethylaminopyridine</topic><topic>DMF, dimethylformamide</topic><topic>DMSO, dimethylsulfoxide</topic><topic>Fundamental and applied biological sciences. 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| fulltext | fulltext |
| identifier | ISSN: 0014-5793 |
| ispartof | FEBS letters, 1990, Vol.259 (2), p.335-337 |
| issn | 0014-5793 1873-3468 |
| language | eng |
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| source | MEDLINE; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
| subjects | Analytical, structural and metabolic biochemistry Autoradiography Base Sequence Biological and medical sciences CMC, N-cyclohexyl-N'-morpholinoethyl carbodiimide metho-p-toluenesulfonate Coproporphyrins DMAP, 4-dimethylaminopyridine DMF, dimethylformamide DMSO, dimethylsulfoxide Fundamental and applied biological sciences. Psychology Molecular Sequence Data Nucleic acids Nucleic bases, nucleotides Oligodeoxyribonucleotides - chemical synthesis Palladium Pd(II)-coproporphyrin I Phosphorus Radioisotopes Photochemistry Photoirradiation Por (COOH)4, palladium (II)-coproporphyrin I Porphyrins Sequence-specific modification |
| title | Palladium(II)-coproporphyrin I as a photoactivable group in sequence-specific modification of nucleic acids by oligonucleotide derivatives |
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