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  1. JBIC Journal of Biological Inorganic Chemistry
  2. JBIC Journal of Biological Inorganic Chemistry : Volume 4
  3. JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 5, October 1999
  4. Double-strand DNA hydrolysis by dilanthanide complexes
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JBIC Journal of Biological Inorganic Chemistry : Volume 22
JBIC Journal of Biological Inorganic Chemistry : Volume 21
JBIC Journal of Biological Inorganic Chemistry : Volume 20
JBIC Journal of Biological Inorganic Chemistry : Volume 19
JBIC Journal of Biological Inorganic Chemistry : Volume 18
JBIC Journal of Biological Inorganic Chemistry : Volume 17
JBIC Journal of Biological Inorganic Chemistry : Volume 16
JBIC Journal of Biological Inorganic Chemistry : Volume 15
JBIC Journal of Biological Inorganic Chemistry : Volume 14
JBIC Journal of Biological Inorganic Chemistry : Volume 13
JBIC Journal of Biological Inorganic Chemistry : Volume 12
JBIC Journal of Biological Inorganic Chemistry : Volume 11
JBIC Journal of Biological Inorganic Chemistry : Volume 10
JBIC Journal of Biological Inorganic Chemistry : Volume 9
JBIC Journal of Biological Inorganic Chemistry : Volume 8
JBIC Journal of Biological Inorganic Chemistry : Volume 7
JBIC Journal of Biological Inorganic Chemistry : Volume 6
JBIC Journal of Biological Inorganic Chemistry : Volume 5
JBIC Journal of Biological Inorganic Chemistry : Volume 4
JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 6, December 1999
JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 5, October 1999
Magnesium transport in prokaryotes
Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction?
Metal ions in non-complementary DNA base pairs: an ab initio study of Cu(I), Ag(I), and Au(I) complexes with the cytosine-adenine base pair
Speciation of trace elements in proteins in human and bovine serum by size exclusion chromatography and inductively coupled plasma-mass spectrometry with a magnetic sector mass spectrometer
The new anticancer drug [(2R )-aminomethylpyrrolidine](1,1-cyclobutanedicarboxylato)platinum(II) and its toxic S enantiomer do interact differently with nucleic acids
Ferredoxin-NADP+ reductase uses the same site for the interaction with ferredoxin and flavodoxin
An X-ray crystallographic study of the binding sites of the azide inhibitor and organic substrates to ceruloplasmin, a multi-copper oxidase in the plasma
Extended X-ray absorption fine structure studies on periplasmic and intracellular molybdenum-binding proteins
Double-strand DNA hydrolysis by dilanthanide complexes
Effects of nonspecific ion-protein interactions on the redox chemistry of cytochrome c
Effect of metal substitution in copper amine oxidase from lentil seedlings
Iron-sulfur interconversions in the anaerobic ribonucleotide reductase from Escherichia coli
Identification of platination sites on human serum transferrin using 13C and 15N NMR spectroscopy
Redox regulation of calcineurin in T-lymphocytes
Trans-(NH3)2PtII-modified deoxyoligonucleotides as potential antisense agents: cross-linking reactions between two 12-mers
The influence of axial ligands on the reduction potential of blue copper proteins
An Electrochemical Study of the Factors Responsible for Modulating the Reduction Potential of Putidaredoxin
JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 4, August 1999
JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 3, July 1999
JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 2, May 1999
JBIC Journal of Biological Inorganic Chemistry : Volume 4, Issue 1, February 1999
JBIC Journal of Biological Inorganic Chemistry : Volume 3
JBIC Journal of Biological Inorganic Chemistry : Volume 2

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Double-strand DNA hydrolysis by dilanthanide complexes

Content Provider Springer Nature Link
Author Branum, Mark E. Que Jr., L.
Copyright Year 1999
Abstract  Although there has been progress in developing artificial hydrolytic DNA cleaving agents, none of these has been shown to carry out the double-strand hydrolysis of DNA. We demonstrate that La(III) or Ce(IV) combined with the ligand 1,3-diamino-2-hydroxypropane-N,N,N′,N′-tetraacetate (HPTA) in a 2 : 1 ratio can efficiently cleave supercoiled plasmid DNA at 55  °C within a 3-h period. Analysis of end-labeled restriction fragments cleaved by these complexes reveals 3′- and 5′-ends consistent with a hydrolytic mechanism. Unlike for other polydentate carboxylate complexes, plasmid DNA cleavage by La2(HPTA) or Ce2(HPTA) affords a significant amount of linear DNA with a considerable fraction of the supercoiled form still remaining. This result implies that La2(HPTA) and Ce2(HPTA) can carry out double-strand cleavage of plasmid DNA. La2(HPTA) and Ce2(HPTA) represent the first metal complexes demonstrated to be capable of double-strand hydrolytic cleavage of plasmid DNA.
Starting Page 593
Ending Page 600
Page Count 8
File Format PDF
ISSN 09498257
Journal JBIC Journal of Biological Inorganic Chemistry
Volume Number 4
Issue Number 5
e-ISSN 14321327
Language English
Publisher Springer-Verlag
Publisher Date 1999-10-18
Publisher Place Berlin, Heidelberg
Access Restriction One Nation One Subscription (ONOS)
Content Type Text
Resource Type Article
Subject Biochemistry Inorganic Chemistry
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