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Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors

Characterization of synthetic oligonucleotides and quantification of primer extension mediated by a human translesion synthesis polymerase η (Pol η) over drug-induced DNA lesions in the presence on modified nucleotide analogs is described. Extent of primer extension for each reaction was monitored b...

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Autores principales: Malvezzi, S., Sturla, S.J., Tanasova, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510374/
https://www.ncbi.nlm.nih.gov/pubmed/26217754
http://dx.doi.org/10.1016/j.dib.2015.04.006
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author Malvezzi, S.
Sturla, S.J.
Tanasova, M.
author_facet Malvezzi, S.
Sturla, S.J.
Tanasova, M.
author_sort Malvezzi, S.
collection PubMed
description Characterization of synthetic oligonucleotides and quantification of primer extension mediated by a human translesion synthesis polymerase η (Pol η) over drug-induced DNA lesions in the presence on modified nucleotide analogs is described. Extent of primer extension for each reaction was monitored by denaturing gel electrophoresis. The data was obtained to assess the performance of the fluorescence-based primer extension (PE-PiPer) assay [1] with respect to the established and conventionally used denaturing gel electrophoresis. The obtained data reflects the specific inhibition of translesion synthesis over cisplatin containing DNA with 5-OH-CTP.
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spelling pubmed-45103742015-07-27 Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors Malvezzi, S. Sturla, S.J. Tanasova, M. Data Brief Data Article Characterization of synthetic oligonucleotides and quantification of primer extension mediated by a human translesion synthesis polymerase η (Pol η) over drug-induced DNA lesions in the presence on modified nucleotide analogs is described. Extent of primer extension for each reaction was monitored by denaturing gel electrophoresis. The data was obtained to assess the performance of the fluorescence-based primer extension (PE-PiPer) assay [1] with respect to the established and conventionally used denaturing gel electrophoresis. The obtained data reflects the specific inhibition of translesion synthesis over cisplatin containing DNA with 5-OH-CTP. Elsevier 2015-04-22 /pmc/articles/PMC4510374/ /pubmed/26217754 http://dx.doi.org/10.1016/j.dib.2015.04.006 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Data Article
Malvezzi, S.
Sturla, S.J.
Tanasova, M.
Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
title Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
title_full Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
title_fullStr Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
title_full_unstemmed Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
title_short Data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
title_sort data in support of quantification of pyrophosphate as a universal approach to determine polymerase activity and assay polymerase inhibitors
topic Data Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4510374/
https://www.ncbi.nlm.nih.gov/pubmed/26217754
http://dx.doi.org/10.1016/j.dib.2015.04.006
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