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<field name="value">Łęczkowska, Anna .</field>
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<field name="value">González García, Jorge .</field>
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<field name="value">Pérez Arnáiz, Cristina</field>
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<field name="confidence">500</field>
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<field name="value">García Ruiz, Begoña</field>
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<field name="value">White, Andrew J. P. .</field>
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<field name="value">Vilar, Ramón .</field>
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<field name="value">2018-09-05T09:24:03Z</field>
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<field name="value">2019-08-09T02:45:06Z</field>
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<field name="value">2018-08</field>
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<field name="value">0947-6539</field>
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<field name="value">10.1002/chem.201802248</field>
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<field name="value">The proposed in vivo formation of G-quadruplex&#xd;
DNA (G4 DNA) in promoter regions of oncogenes and in telomeres&#xd;
has prompted the development of small molecules&#xd;
with high affinity and selectivity for these structures. Herein&#xd;
we report the synthesis of a new di-substituted bipyridine&#xd;
ligand and the corresponding complexes with Ni2+ and&#xd;
VO2+. Both these new complexes have been characterized&#xd;
spectroscopically and by X-ray crystallography. Detailed DNA&#xd;
binding studies of these two complexes, together with three&#xd;
previously reported metal salphen complexes, are presented.&#xd;
Using FRET melting assays, the binding affinity and selectivity&#xd;
of the five metal complexes against six different G4 DNA&#xd;
structures as well as a duplex DNA have been determined.&#xd;
In addition, we present detailed ITC and UV/Vis studies to&#xd;
characterize the interaction of the complexes with human&#xd;
telomeric G4 DNA. Finally, we show via a polymerase stop&#xd;
assay that these complexes are able to stabilize a G4 DNA&#xd;
structure (from the c-Myc oncogene promoter) and halt the&#xd;
activity of Taq polymerase.</field>
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<field name="value">UK’s Engineering and Physical Sciences Research Council&#xd;
(EPSRC) (grant number: EP/H005285/1)</field>
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<field name="value">eng</field>
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<field name="value">Wiley-VCH Verlag</field>
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<field name="value">Chemistry-a european journal. 2018, V. 24, n. 45, p. 11785-11794</field>
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<field name="value">https://doi.org/10.1002/chem.201802248</field>
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<field name="value">cancer</field>
<field name="value">DNA binding</field>
<field name="value">heterocycles</field>
<field name="value">metal complexes</field>
<field name="value">polymerase</field>
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<element name="title">
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<field name="value">Binding studies of metal–salphen and metal–bipyridine complexes towards G‐Quadruplex DNA</field>
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