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Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay

Using a gel mobility shift assay, we have identified proteins, in the nuclear extracts of a human lung cancer cell line, that recognize cis‐diamminedichloroplatinum(II) (cis‐DDP, CDDP)‐modified DNA. A 158‐base‐pair double‐stranded DNA fragment, derived from pBR322 plasmid DNA, was modified by either...

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Autores principales: Fujiwara, Yasuhiro, Kasahara, Kazuo, Sugimoto, Yoshikazu, Nishio, Kazuto, Ohmori, Tohru, Saijo, Nagahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1990
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918002/
https://www.ncbi.nlm.nih.gov/pubmed/2125989
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02680.x
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author Fujiwara, Yasuhiro
Kasahara, Kazuo
Sugimoto, Yoshikazu
Nishio, Kazuto
Ohmori, Tohru
Saijo, Nagahiro
author_facet Fujiwara, Yasuhiro
Kasahara, Kazuo
Sugimoto, Yoshikazu
Nishio, Kazuto
Ohmori, Tohru
Saijo, Nagahiro
author_sort Fujiwara, Yasuhiro
collection PubMed
description Using a gel mobility shift assay, we have identified proteins, in the nuclear extracts of a human lung cancer cell line, that recognize cis‐diamminedichloroplatinum(II) (cis‐DDP, CDDP)‐modified DNA. A 158‐base‐pair double‐stranded DNA fragment, derived from pBR322 plasmid DNA, was modified by either CDDP, tetrachloro(dl‐trans)‐1,2‐diaminocyclohexaneplatinum(IV) (tetraplatin) or trans‐DDP (the stereoisomer of CDDP and clinically ineffective). These platinum drug‐modified probes were incubated with nuclear extracts and analyzed by gel mobility shift assay. Proteins in the extracts selectively recognized the clinically active platinum‐modified DNA fragment. No binding to the trans‐DDP‐modified DNA fragment was observed. These proteins may play a role in the cytotoxicity or in a DNA repair process.
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spelling pubmed-59180022018-05-11 Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay Fujiwara, Yasuhiro Kasahara, Kazuo Sugimoto, Yoshikazu Nishio, Kazuto Ohmori, Tohru Saijo, Nagahiro Jpn J Cancer Res Rapid Communication Using a gel mobility shift assay, we have identified proteins, in the nuclear extracts of a human lung cancer cell line, that recognize cis‐diamminedichloroplatinum(II) (cis‐DDP, CDDP)‐modified DNA. A 158‐base‐pair double‐stranded DNA fragment, derived from pBR322 plasmid DNA, was modified by either CDDP, tetrachloro(dl‐trans)‐1,2‐diaminocyclohexaneplatinum(IV) (tetraplatin) or trans‐DDP (the stereoisomer of CDDP and clinically ineffective). These platinum drug‐modified probes were incubated with nuclear extracts and analyzed by gel mobility shift assay. Proteins in the extracts selectively recognized the clinically active platinum‐modified DNA fragment. No binding to the trans‐DDP‐modified DNA fragment was observed. These proteins may play a role in the cytotoxicity or in a DNA repair process. Blackwell Publishing Ltd 1990-12 /pmc/articles/PMC5918002/ /pubmed/2125989 http://dx.doi.org/10.1111/j.1349-7006.1990.tb02680.x Text en
spellingShingle Rapid Communication
Fujiwara, Yasuhiro
Kasahara, Kazuo
Sugimoto, Yoshikazu
Nishio, Kazuto
Ohmori, Tohru
Saijo, Nagahiro
Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay
title Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay
title_full Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay
title_fullStr Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay
title_full_unstemmed Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay
title_short Detection of Proteins that Recognize Platinum‐modified DNA Using Gel Mobility Shift Assay
title_sort detection of proteins that recognize platinum‐modified dna using gel mobility shift assay
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918002/
https://www.ncbi.nlm.nih.gov/pubmed/2125989
http://dx.doi.org/10.1111/j.1349-7006.1990.tb02680.x
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