DNA binding and cleavage studies of copper(II) complexes with 2′-deoxyadenosine modified histidine moiety

Verfasser / Beitragende:
[Justyna Borowska, Malgorzata Sierant, Elzbieta Sochacka, Daniele Sanna, Elzbieta Lodyga-Chruscinska]
Ort, Verlag, Jahr:
2015
Enthalten in:
JBIC Journal of Biological Inorganic Chemistry, 20/6(2015-09-01), 989-1004
Format:
Artikel (online)
ID: 605507058
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024 7 0 |a 10.1007/s00775-015-1282-2  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00775-015-1282-2 
245 0 0 |a DNA binding and cleavage studies of copper(II) complexes with 2′-deoxyadenosine modified histidine moiety  |h [Elektronische Daten]  |c [Justyna Borowska, Malgorzata Sierant, Elzbieta Sochacka, Daniele Sanna, Elzbieta Lodyga-Chruscinska] 
520 3 |a This work is focused on the study of DNA binding and cleavage properties of 2′-deoxyadenosines modified with ester/amide of histidine (his6dA ester, his6dA amide) and their copper(II) complexes. To determine the coordination mode of the complex species potentiometric and spectroscopic (UV-visible, CD, EPR) studies have been performed. The analysis of electronic absorption and fluorescence spectra has been used to find the nature of the interactions between the compounds and calf thymus DNA (CT-DNA). There is significant influence of the -NH2 and -OCH3 groups on binding of the ligands or the complexes to DNA. Only amide derivative and its complex reveal intercalative ability. In the case of his6dA ester and Cu(II)-his6dA ester the main interactions can be groove binding. DNA cleavage activities of the compounds have been examined by gel electrophoresis. The copper complexes have promoted the cleavage of plasmid DNA, but none of the ligands exhibited any chemical nuclease activity. The application of different scavengers of reactive oxygen species provided a conclusion that DNA cleavage caused by copper complexes might occur via hydrolytic pathway. 
540 |a SBIC, 2015 
690 7 |a Artificial nucleases  |2 nationallicence 
690 7 |a Copper complexes  |2 nationallicence 
690 7 |a Histidine derivatives  |2 nationallicence 
700 1 |a Borowska  |D Justyna  |u Institute of General Food Chemistry, Lodz University of Technology, ul. Stefanowskiego 4/10, 90-924, Lodz, Poland  |4 aut 
700 1 |a Sierant  |D Malgorzata  |u Centre of Molecular and Macromolecular Studies, Polish Academy of Science, ul. Sienkiewicza 112, 90-363, Lodz, Poland  |4 aut 
700 1 |a Sochacka  |D Elzbieta  |u Institute of Organic Chemistry, Lodz University of Technology, ul. Zeromskiego 176, 90-924, Lodz, Poland  |4 aut 
700 1 |a Sanna  |D Daniele  |u Istituto C.N.R. Chimica Biomolecolare, Trav. La Crucca 3, reg. Baldinca, 07040, Sassari, Italy  |4 aut 
700 1 |a Lodyga-Chruscinska  |D Elzbieta  |u Institute of General Food Chemistry, Lodz University of Technology, ul. Stefanowskiego 4/10, 90-924, Lodz, Poland  |4 aut 
773 0 |t JBIC Journal of Biological Inorganic Chemistry  |d Springer Berlin Heidelberg  |g 20/6(2015-09-01), 989-1004  |x 0949-8257  |q 20:6<989  |1 2015  |2 20  |o 775 
856 4 0 |u https://doi.org/10.1007/s00775-015-1282-2  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
949 |B NATIONALLICENCE  |F NATIONALLICENCE  |b NL-springer 
950 |B NATIONALLICENCE  |P 856  |E 40  |u https://doi.org/10.1007/s00775-015-1282-2  |q text/html  |z Onlinezugriff via DOI 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Borowska  |D Justyna  |u Institute of General Food Chemistry, Lodz University of Technology, ul. Stefanowskiego 4/10, 90-924, Lodz, Poland  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sierant  |D Malgorzata  |u Centre of Molecular and Macromolecular Studies, Polish Academy of Science, ul. Sienkiewicza 112, 90-363, Lodz, Poland  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sochacka  |D Elzbieta  |u Institute of Organic Chemistry, Lodz University of Technology, ul. Zeromskiego 176, 90-924, Lodz, Poland  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Sanna  |D Daniele  |u Istituto C.N.R. Chimica Biomolecolare, Trav. La Crucca 3, reg. Baldinca, 07040, Sassari, Italy  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Lodyga-Chruscinska  |D Elzbieta  |u Institute of General Food Chemistry, Lodz University of Technology, ul. Stefanowskiego 4/10, 90-924, Lodz, Poland  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t JBIC Journal of Biological Inorganic Chemistry  |d Springer Berlin Heidelberg  |g 20/6(2015-09-01), 989-1004  |x 0949-8257  |q 20:6<989  |1 2015  |2 20  |o 775