A protein-mediated mechanism for the DNA sequence-specific action of topoisomerase II poisons. (Q41622531)

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7 November 2019

review article

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title

A protein-mediated mechanism for the DNA sequence-specific action of topoisomerase II poisons (English)

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7 November 2019

5

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7 November 2019

Giovanni Capranico

1

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7 November 2019

author name string

M Binaschi

2

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7 November 2019

M E Borgnetto

3

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7 November 2019

F Zunino

4

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7 November 2019

publication date

1 September 1997

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Trends in Pharmacological Sciences

7 November 2019

published in

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7 November 2019

volume

18

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7 November 2019

issue

9

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7 November 2019

page(s)

323-329

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7 November 2019

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The mechanisms of DNA topoisomerases

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Structure and mechanism of DNA topoisomerase II

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Crystal structure of an N-terminal fragment of the DNA gyrase B protein.

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Structure and conformational changes of DNA topoisomerase II visualized by electron microscopy

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Effects of antineoplastic drugs on the post-strand-passage DNA cleavage/religation equilibrium of topoisomerase II.

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Topoisomerase II.etoposide interactions direct the formation of drug-induced enzyme-DNA cleavage complexes.

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The basis for camptothecin enhancement of DNA breakage by eukaryotic topoisomerase I.

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DNA topoisomerase poisons as antitumor drugs

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DNA topoisomerase-trapping antitumour drugs

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Antitumor bisdioxopiperazines inhibit yeast DNA topoisomerase II by trapping the enzyme in the form of a closed protein clamp

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Local sequence requirements for DNA cleavage by mammalian topoisomerase II in the presence of doxorubicin.

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Localization of an aminoacridine antitumor agent in a type II topoisomerase-DNA complex

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Interaction of an alkylating camptothecin derivative with a DNA base at topoisomerase I-DNA cleavage sites

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Conformational drug determinants of the sequence specificity of drug-stimulated topoisomerase II DNA cleavage

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Competitive inhibition of nicking—closing enzymes may explain some biological effects of DNA intercalators

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Topoisomerase II binds to ellipticine in the absence or presence of DNA. Characterization of enzyme-drug interactions by fluorescence spectroscopy

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Study of allosteric communication between protomers by immunotagging

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Base mutation analysis of topoisomerase II-idarubicin-DNA ternary complex formation. Evidence for enzyme subunit cooperativity in DNA cleavage

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Base sequence determinants of amonafide stimulation of topoisomerase II DNA cleavage.

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Local base sequence preferences for DNA cleavage by mammalian topoisomerase II in the presence of amsacrine or teniposide.

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DNA sequence specificity of mitoxantrone

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Preferential binding of daunomycin to 5'ATCG and 5'ATGC sequences revealed by footprinting titration experiments

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Interactions between an anthracycline antibiotic and DNA: molecular structure of daunomycin complexed to d(CpGpTpApCpG) at 1.2-A resolution

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Energetics and stereochemistry of DNA complexation with the antitumor AT specific intercalators tilorone and m-AMSA

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Direct recognition of the trp operator by the trp holorepressor--a review

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Electrostatic activation of Escherichia coli methionine repressor

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The crystal structure of the estrogen receptor DNA-binding domain bound to DNA: how receptors discriminate between their response elements

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Crystal structure of trp repressor/operator complex at atomic resolution

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How proteins recognize the TATA box

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Substrate structure influences binding of the non-histone protein HMG-I(Y) to free nucleosomal DNA

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Resolving the role of topoisomerase II in chromatin structure and function

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In vitro selection of aptamers: the dearth of pure reason

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DNA minor groove-binding ligands: a different class of mammalian DNA topoisomerase I inhibitors.

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Quinolone binding to DNA is mediated by magnesium ions

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Identifiers

DOI

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7 November 2019

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