Restriction‐enzyme cleavage of DNA modified by platinum(II) complexes

The effect of binding of cis‐diamminedichloroplatinum(II), its trans isomer and diethylenetriami‐nechloroplatinum(II) chloride to DNA on the splicing effectiveness of BamHI, EcoRI and SalI restriction endonucleases has been determined by means of gel electrophoresis. All three platinum complexes inh...

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Veröffentlicht in:European journal of biochemistry 1993-08, Vol.216 (1), p.183-187
Hauptverfasser: BRABEC, Viktor, BALCAROVA, Zdenka
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container_title European journal of biochemistry
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creator BRABEC, Viktor
BALCAROVA, Zdenka
description The effect of binding of cis‐diamminedichloroplatinum(II), its trans isomer and diethylenetriami‐nechloroplatinum(II) chloride to DNA on the splicing effectiveness of BamHI, EcoRI and SalI restriction endonucleases has been determined by means of gel electrophoresis. All three platinum complexes inhibit the cleavage of linearized plasmid DNA. In addition, the three platinum complexes bound to DNA constitute a barrier across which the linear diffusion of EcoRI on DNA is difficult. We interprete these findings to mean that the splicing effectiveness of restriction enzymes is influenced by bifunctional and monofunctional DNA adducts of platinum via both steric interference and DNA conformational distortions. Whereas the platinum adducts in the restriction sites or in their very close proximity inhibit the cleavage, the lesions occurring a greater distance from the restriction site can slow down the process of the localization of recognition sequences.
doi_str_mv 10.1111/j.1432-1033.1993.tb18131.x
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All three platinum complexes inhibit the cleavage of linearized plasmid DNA. In addition, the three platinum complexes bound to DNA constitute a barrier across which the linear diffusion of EcoRI on DNA is difficult. We interprete these findings to mean that the splicing effectiveness of restriction enzymes is influenced by bifunctional and monofunctional DNA adducts of platinum via both steric interference and DNA conformational distortions. 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Whereas the platinum adducts in the restriction sites or in their very close proximity inhibit the cleavage, the lesions occurring a greater distance from the restriction site can slow down the process of the localization of recognition sequences.</description><subject>Antineoplastic agents</subject><subject>Binding Sites</subject><subject>Biological and medical sciences</subject><subject>Cisplatin - pharmacology</subject><subject>Deoxyribonuclease BamHI - metabolism</subject><subject>Deoxyribonuclease EcoRI - metabolism</subject><subject>Deoxyribonucleases, Type II Site-Specific - metabolism</subject><subject>DNA - metabolism</subject><subject>Electrophoresis, Agar Gel</subject><subject>General aspects</subject><subject>Medical sciences</subject><subject>Organoplatinum Compounds - pharmacology</subject><subject>Pharmacology. 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Drug treatments</topic><topic>Plasmids - drug effects</topic><topic>Stereoisomerism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BRABEC, Viktor</creatorcontrib><creatorcontrib>BALCAROVA, Zdenka</creatorcontrib><collection>Pascal-Francis</collection><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>European journal of biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BRABEC, Viktor</au><au>BALCAROVA, Zdenka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Restriction‐enzyme cleavage of DNA modified by platinum(II) complexes</atitle><jtitle>European journal of biochemistry</jtitle><addtitle>Eur J Biochem</addtitle><date>1993-08-15</date><risdate>1993</risdate><volume>216</volume><issue>1</issue><spage>183</spage><epage>187</epage><pages>183-187</pages><issn>0014-2956</issn><eissn>1432-1033</eissn><coden>EJBCAI</coden><abstract>The effect of binding of cis‐diamminedichloroplatinum(II), its trans isomer and diethylenetriami‐nechloroplatinum(II) chloride to DNA on the splicing effectiveness of BamHI, EcoRI and SalI restriction endonucleases has been determined by means of gel electrophoresis. 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subjects Antineoplastic agents
Binding Sites
Biological and medical sciences
Cisplatin - pharmacology
Deoxyribonuclease BamHI - metabolism
Deoxyribonuclease EcoRI - metabolism
Deoxyribonucleases, Type II Site-Specific - metabolism
DNA - metabolism
Electrophoresis, Agar Gel
General aspects
Medical sciences
Organoplatinum Compounds - pharmacology
Pharmacology. Drug treatments
Plasmids - drug effects
Stereoisomerism
title Restriction‐enzyme cleavage of DNA modified by platinum(II) complexes
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