Copper(II) complexes with Fusobacterium nucleatum adhesin FadA: Coordination pattern, physicochemical properties and reactivity
Fusobacterium nucleatum is an anaerobic, Gram-negative bacteria linked to colon cancer. It is interesting to determine how metal ions interact with bacterial adhesin proteins. To this end, the coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was...
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Veröffentlicht in: | Journal of inorganic biochemistry 2018-12, Vol.189, p.69-80 |
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creator | Krupa, Katarzyna Lesiów, Monika Stokowa-Sołtys, Kamila Starosta, Radosław Ptaszyńska, Natalia Łęgowska, Anna Rolka, Krzysztof Wernecki, Maciej Cal, Magdalena Jeżowska-Bojczuk, Małgorzata |
description | Fusobacterium nucleatum is an anaerobic, Gram-negative bacteria linked to colon cancer. It is interesting to determine how metal ions interact with bacterial adhesin proteins. To this end, the coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by potentiometry, spectroscopic techniques (UV–Vis, CD, EPR and NMR) and the density functional theory (DFT) methods. At pH 6.8 (colon physiological pH), the metal ion in the first peptide (ATDAAS-NH2) is coordinated by one oxygen and three nitrogen donors while in the second one (MKKFL-NH2) - by sulfur and three nitrogen atoms. Both complexes form two five- and one six-membered stable chelate rings. Moreover, reactivity studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. Generation of reactive oxygen species (ROS) was observed during gel electrophoresis and spectroscopic assays with reporting molecules like NDMA (N,N-dimethyl-p-nitrosoaniline) and NBT (Nitrotetrazolium Blue Chloride). All reactions were conducted in the presence of hydrogen peroxide as endogenous oxidant.
The coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by experimental and computational methods. Moreover, the studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. [Display omitted]
•Chemical studies on fragments of Fusobacterium adhesion A (FadA)•Potentiometric and spectroscopic characteristic of Cu(II)-FadA fragments•Degradation of the plasmid DNA in the presence of the complexes•Identification of generated reactive oxygen species |
doi_str_mv | 10.1016/j.jinorgbio.2018.09.012 |
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The coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by experimental and computational methods. Moreover, the studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. [Display omitted]
•Chemical studies on fragments of Fusobacterium adhesion A (FadA)•Potentiometric and spectroscopic characteristic of Cu(II)-FadA fragments•Degradation of the plasmid DNA in the presence of the complexes•Identification of generated reactive oxygen species</description><identifier>ISSN: 0162-0134</identifier><identifier>EISSN: 1873-3344</identifier><identifier>DOI: 10.1016/j.jinorgbio.2018.09.012</identifier><identifier>PMID: 30243120</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adhesins, Bacterial - chemistry ; Copper - chemistry ; Electron Spin Resonance Spectroscopy ; Fusobacterium nucleatum - chemistry ; Hydrogen-Ion Concentration ; Potentiometry ; Reactive Oxygen Species - chemistry ; Superoxides - chemistry</subject><ispartof>Journal of inorganic biochemistry, 2018-12, Vol.189, p.69-80</ispartof><rights>2018 Elsevier Inc.</rights><rights>Copyright © 2018 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-849ca22c021853bb9a4510c156c0195a53a6115c7651e71405b8357d9a7eba4a3</citedby><cites>FETCH-LOGICAL-c408t-849ca22c021853bb9a4510c156c0195a53a6115c7651e71405b8357d9a7eba4a3</cites><orcidid>0000-0003-4821-5898</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jinorgbio.2018.09.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30243120$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krupa, Katarzyna</creatorcontrib><creatorcontrib>Lesiów, Monika</creatorcontrib><creatorcontrib>Stokowa-Sołtys, Kamila</creatorcontrib><creatorcontrib>Starosta, Radosław</creatorcontrib><creatorcontrib>Ptaszyńska, Natalia</creatorcontrib><creatorcontrib>Łęgowska, Anna</creatorcontrib><creatorcontrib>Rolka, Krzysztof</creatorcontrib><creatorcontrib>Wernecki, Maciej</creatorcontrib><creatorcontrib>Cal, Magdalena</creatorcontrib><creatorcontrib>Jeżowska-Bojczuk, Małgorzata</creatorcontrib><title>Copper(II) complexes with Fusobacterium nucleatum adhesin FadA: Coordination pattern, physicochemical properties and reactivity</title><title>Journal of inorganic biochemistry</title><addtitle>J Inorg Biochem</addtitle><description>Fusobacterium nucleatum is an anaerobic, Gram-negative bacteria linked to colon cancer. It is interesting to determine how metal ions interact with bacterial adhesin proteins. To this end, the coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by potentiometry, spectroscopic techniques (UV–Vis, CD, EPR and NMR) and the density functional theory (DFT) methods. At pH 6.8 (colon physiological pH), the metal ion in the first peptide (ATDAAS-NH2) is coordinated by one oxygen and three nitrogen donors while in the second one (MKKFL-NH2) - by sulfur and three nitrogen atoms. Both complexes form two five- and one six-membered stable chelate rings. Moreover, reactivity studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. Generation of reactive oxygen species (ROS) was observed during gel electrophoresis and spectroscopic assays with reporting molecules like NDMA (N,N-dimethyl-p-nitrosoaniline) and NBT (Nitrotetrazolium Blue Chloride). All reactions were conducted in the presence of hydrogen peroxide as endogenous oxidant.
The coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by experimental and computational methods. Moreover, the studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. [Display omitted]
•Chemical studies on fragments of Fusobacterium adhesion A (FadA)•Potentiometric and spectroscopic characteristic of Cu(II)-FadA fragments•Degradation of the plasmid DNA in the presence of the complexes•Identification of generated reactive oxygen species</description><subject>Adhesins, Bacterial - chemistry</subject><subject>Copper - chemistry</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>Fusobacterium nucleatum - chemistry</subject><subject>Hydrogen-Ion Concentration</subject><subject>Potentiometry</subject><subject>Reactive Oxygen Species - chemistry</subject><subject>Superoxides - chemistry</subject><issn>0162-0134</issn><issn>1873-3344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1u1DAURi0EotPCK4CXRSLB1z-ThN1oxJSRKrGBteU4t4xHiR1sp2VWvDqupnSLN_bi3O-7PoS8B1YDg_WnY310PsSfvQs1Z9DWrKsZ8BdkBW0jKiGkfElWheQVAyEvyGVKR8aYUrJ5TS4E41IAZyvyZxvmGeP1fv-B2jDNI_7GRB9cPtDdkkJvbMbolon6xY5ocnmZ4YDJebozw-Yz3YYQB-dNdsHT2eSC-490PpySs8EecHLWjHSOobRkV7KNH2jEkuvuXT69Ia_uzJjw7dN9RX7svnzffq1uv93st5vbykrW5qqVnTWcW8ahVaLvOyMVMAtqbRl0yihh1gDKNmsF2IBkqm-FaobONNgbacQVuT7nlk1-LZiynlyyOI7GY1iS5lCObEDJgjZn1MaQUsQ7PUc3mXjSwPSjfX3Uz_b1o33NOl3sl8l3TyVLP-HwPPdPdwE2ZwDLV-8dRp2sQ29xcBFt1kNw_y35C5V-m-k</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Krupa, Katarzyna</creator><creator>Lesiów, Monika</creator><creator>Stokowa-Sołtys, Kamila</creator><creator>Starosta, Radosław</creator><creator>Ptaszyńska, Natalia</creator><creator>Łęgowska, Anna</creator><creator>Rolka, Krzysztof</creator><creator>Wernecki, Maciej</creator><creator>Cal, Magdalena</creator><creator>Jeżowska-Bojczuk, Małgorzata</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><orcidid>https://orcid.org/0000-0003-4821-5898</orcidid></search><sort><creationdate>20181201</creationdate><title>Copper(II) complexes with Fusobacterium nucleatum adhesin FadA: Coordination pattern, physicochemical properties and reactivity</title><author>Krupa, Katarzyna ; Lesiów, Monika ; Stokowa-Sołtys, Kamila ; Starosta, Radosław ; Ptaszyńska, Natalia ; Łęgowska, Anna ; Rolka, Krzysztof ; Wernecki, Maciej ; Cal, Magdalena ; Jeżowska-Bojczuk, Małgorzata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-849ca22c021853bb9a4510c156c0195a53a6115c7651e71405b8357d9a7eba4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adhesins, Bacterial - chemistry</topic><topic>Copper - chemistry</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>Fusobacterium nucleatum - chemistry</topic><topic>Hydrogen-Ion Concentration</topic><topic>Potentiometry</topic><topic>Reactive Oxygen Species - chemistry</topic><topic>Superoxides - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krupa, Katarzyna</creatorcontrib><creatorcontrib>Lesiów, Monika</creatorcontrib><creatorcontrib>Stokowa-Sołtys, Kamila</creatorcontrib><creatorcontrib>Starosta, Radosław</creatorcontrib><creatorcontrib>Ptaszyńska, Natalia</creatorcontrib><creatorcontrib>Łęgowska, Anna</creatorcontrib><creatorcontrib>Rolka, Krzysztof</creatorcontrib><creatorcontrib>Wernecki, Maciej</creatorcontrib><creatorcontrib>Cal, Magdalena</creatorcontrib><creatorcontrib>Jeżowska-Bojczuk, Małgorzata</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>Journal of inorganic biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krupa, Katarzyna</au><au>Lesiów, Monika</au><au>Stokowa-Sołtys, Kamila</au><au>Starosta, Radosław</au><au>Ptaszyńska, Natalia</au><au>Łęgowska, Anna</au><au>Rolka, Krzysztof</au><au>Wernecki, Maciej</au><au>Cal, Magdalena</au><au>Jeżowska-Bojczuk, Małgorzata</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Copper(II) complexes with Fusobacterium nucleatum adhesin FadA: Coordination pattern, physicochemical properties and reactivity</atitle><jtitle>Journal of inorganic biochemistry</jtitle><addtitle>J Inorg Biochem</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>189</volume><spage>69</spage><epage>80</epage><pages>69-80</pages><issn>0162-0134</issn><eissn>1873-3344</eissn><abstract>Fusobacterium nucleatum is an anaerobic, Gram-negative bacteria linked to colon cancer. It is interesting to determine how metal ions interact with bacterial adhesin proteins. To this end, the coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by potentiometry, spectroscopic techniques (UV–Vis, CD, EPR and NMR) and the density functional theory (DFT) methods. At pH 6.8 (colon physiological pH), the metal ion in the first peptide (ATDAAS-NH2) is coordinated by one oxygen and three nitrogen donors while in the second one (MKKFL-NH2) - by sulfur and three nitrogen atoms. Both complexes form two five- and one six-membered stable chelate rings. Moreover, reactivity studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. Generation of reactive oxygen species (ROS) was observed during gel electrophoresis and spectroscopic assays with reporting molecules like NDMA (N,N-dimethyl-p-nitrosoaniline) and NBT (Nitrotetrazolium Blue Chloride). All reactions were conducted in the presence of hydrogen peroxide as endogenous oxidant.
The coordination of ATDAAS-NH2 and MKKFL-NH2 fragments of Fusobacterium adhesin A (FadA) to copper(II) ions was studied by experimental and computational methods. Moreover, the studies confirmed the production of reactive oxygen species such as hydroxyl radical, superoxide anion radical and singlet oxygen. [Display omitted]
•Chemical studies on fragments of Fusobacterium adhesion A (FadA)•Potentiometric and spectroscopic characteristic of Cu(II)-FadA fragments•Degradation of the plasmid DNA in the presence of the complexes•Identification of generated reactive oxygen species</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30243120</pmid><doi>10.1016/j.jinorgbio.2018.09.012</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-4821-5898</orcidid></addata></record> |
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subjects | Adhesins, Bacterial - chemistry Copper - chemistry Electron Spin Resonance Spectroscopy Fusobacterium nucleatum - chemistry Hydrogen-Ion Concentration Potentiometry Reactive Oxygen Species - chemistry Superoxides - chemistry |
title | Copper(II) complexes with Fusobacterium nucleatum adhesin FadA: Coordination pattern, physicochemical properties and reactivity |
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