Literature DB >> 7867796

The monoclonal antibody specific for the 4-hydroxy-2-nonenal histidine adduct.

S Toyokuni1, N Miyake, H Hiai, M Hagiwara, S Kawakishi, T Osawa, K Uchida.   

Abstract

Monoclonal antibodies directed against proteins modified with the major membrane lipid peroxidation product, 4-hydroxy-2-nonenal, have been established and characterized. The monoclonal antibodies specific for HNE-modified proteins were raised by immunizing mice with a HNE-keyhole limpet hemocyanin conjugate. The resulting five monoclonal antibodies (mAbs HNEJ-1-5) recognized HNE-modified bovine serum albumin (BSA), but not native BSA in Western blot studies. Of the five mAbs, HNEJ-2 exhibited the highest affinity for HNE-modified proteins and a much higher affinity for the HNE-histidine adduct than the HNE-lysine or HNE-cysteine adducts. mAb HNEJ-2 did not cross-react with proteins that had been treated with other aldehydes, such as 1-hexenal, 2-hexenal, 4-hydroxy-2-hexenal, 2-nonenal, formaldehyde, or glutaraldehyde. These results suggest that the major epitope recognized by mAb HNEJ-2 is the Michael addition-type HNE-histidine adduct.

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Year:  1995        PMID: 7867796     DOI: 10.1016/0014-5793(95)00033-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  41 in total

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8.  Detection and quantification of protein adduction by electrophilic fatty acids: mitochondrial generation of fatty acid nitroalkene derivatives.

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10.  Oxidative and nitrosative stress in the diaphragm of patients with COPD.

Authors:  Hanneke J H Wijnhoven; Leo M A Heunks; Maartje C P Geraedts; Theo Hafmans; José R Viña; P N Richard Dekhuijzen
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