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Efficient plasmid DNA cleavage by a mononuclear Cu(II) complex

SISSI C.
•
MANCIN F.
•
GATOS M.
altro
TONELLATO U.
2005
  • journal article

Periodico
INORGANIC CHEMISTRY
Abstract
The Cu(II) complex of the ligand all-cis-2,4,6-triamino-1,3,5-trihydroxycyclohexane (TACI) is a very efficient catalyst of the cleavage of plasmid DNA in the absence of any added cofactor. The maximum rate of degradation of the supercoiled plasmid DNA form, obtained at pH 8.1 and 37 °C, in the presence of 48 íM TACIâCuII, is 2.3 ́ 10-3 s-1, corresponding to a half-life time of only 5 min for the cleavage of form I (supercoiled) to form II (relaxed circular). The dependence of the rate of plasmid DNA cleavage from the TACIâCuII complex concentration follows an unusual and very narrow bell-like profile, which suggests an high DNA affinity of the complexes but also a great tendency to form unreactive dimers. The reactivity of the TACIâCuII complexes is not affected by the presence of several scavengers for reactive oxygen species or when measured under anaerobic conditions. Moreover, no degradation of the radical reporter Rhodamine B is observed in the presence of such complexes. These results are consistent with the operation of a prevailing hydrolytic pathway under the normal conditions used, although the failure to obtain enzymatic religation of the linearized DNA does not allow one to rule out the occurrence of a nonhydrolytic oxygen-independent cleavage. A concurrent oxidative mechanism becomes competitive upon addition of reductants or in the presence of high levels of molecular oxygen: under such conditions, in fact, a remarkable increase in the rate of DNA cleavage is observed.
DOI
10.1021/ic049316o
Archivio
http://hdl.handle.net/11368/1701696
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-16244423672
Diritti
metadata only access
Soggetti
  • DNA cleavage

  • artificial nuclease

  • Cu(II)

Scopus© citazioni
113
Data di acquisizione
Jun 7, 2022
Vedi dettagli
Web of Science© citazioni
111
Data di acquisizione
Mar 27, 2024
Visualizzazioni
2
Data di acquisizione
Apr 19, 2024
Vedi dettagli
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