Literature DB >> 2044182

The isolation of monoclonal antibodies selected for the detection of imidazole ring-opened N7-ethylguanine in purified DNA and in cells in situ. Crossreaction with methyl, 2-hydroxyethyl and sulphur mustard adducts.

J H van Delft1, E J van Weert, M M Schellekens, E Claassen, R A Baan.   

Abstract

Monoclonal antibodies have been obtained against imidazole ring-opened N7-ethylguanine (RON7-EtGua) in DNA. The antibodies were selected for good performance in the ELISA with either DNA or nucleated blood cells as immobilized antigen. Antibodies thus selected were studied for their suitability for the in situ detection of RON7-EtGua in the nuclei of cells by means of immunofluorescence microscopy (IFM). Two antibodies have been characterized in detail with respect to specificity and sensitivity. Competitive ELISA demonstrated that the antibodies recognize not only RON7-EtGua but also the corresponding methyl and 2-hydroxyethyl components, with efficiencies that vary with the chemical environment (base, nucleoside or DNA), the nature of the alkyl group and the antibody. They have a clear specificity for the ring-opened alkyl adducts and show an at least 100-fold stronger preference for such structures in DNA when compared to the free nucleoside adducts. Furthermore, they hardly bind to non-alkylated DNA, and do not bind to guanosine or N1- or O6-ethylguanosine. Analysis by DNA-ELISA showed that the binding preference of antibody N7E-026 for ring-opened alkyl adducts is methyl approximately ethyl greater than 2-hydroxyethyl much greater than sulphur mustard, while that of N7E-102 is 2-hydroxyethyl greater than ethyl greater than methyl approximately sulphur mustard. Analysis of RON7-EtGua in DNA with competitive ELISA, DNA-ELISA and IFM showed that in all cases the lowest detection limit can be reached with antibody N7E-026. Competitive ELISA was the most sensitive method, followed by DNA-ELISA and IFM, with detection limits of 2.2, 16 and 23 RON7-EtGua/10(6) nucleotides respectively. In the DNA-ELISA, 12 methyl adducts/10(6) nucleotides can be detected with N7E-026 and 11 2-hydroxyethyl adducts/10(6) nucleotides with N7E-102.

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Year:  1991        PMID: 2044182     DOI: 10.1093/carcin/12.6.1041

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  4 in total

1.  Production and characterization of monoclonal antibodies to N7-phenylguanine.

Authors:  C Schell; C Verkoyen; E Krewet; G Müller; K Norpoth
Journal:  J Cancer Res Clin Oncol       Date:  1993       Impact factor: 4.553

2.  Chemical Biology of N5-Substituted Formamidopyrimidine DNA Adducts.

Authors:  Suresh S Pujari; Natalia Tretyakova
Journal:  Chem Res Toxicol       Date:  2016-12-13       Impact factor: 3.739

3.  Determining N7-alkylguanine adducts by immunochemical methods and HPLC with electrochemical detection: applications in animal studies and in monitoring human exposure to alkylating agents.

Authors:  J H van Delft; M J van Winden; A M van den Ende; R A Baan
Journal:  Environ Health Perspect       Date:  1993-03       Impact factor: 9.031

4.  Repair of O6-alkylguanines in the nuclear DNA of human lymphocytes and leukaemic cells: analysis at the single-cell level.

Authors:  J Thomale; F Seiler; M R Müller; S Seeber; M F Rajewsky
Journal:  Br J Cancer       Date:  1994-04       Impact factor: 7.640

  4 in total

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