| Literature DB >> 7935497 |
E Döring1, R Stigler, G Grütz, R von Baehr, J Schneider-Mergener.
Abstract
Peptides derived from the CDRs of the anti-TNF alpha monoclonal antibody Di62 were tested for inhibition of binding of Di62 to TNF alpha as well as of TNF alpha to its 55 and 75 kDa receptor. A peptide derived from the CDR1 of the light chain was shown to specifically inhibit Di62 binding to TNF alpha with markedly higher activity (Ki = 4 microM) than all other CDR-derived peptides. This peptide also significantly inhibited binding of TNF alpha to its 55 and 75 kDa receptor and protected L929 cells from the cytotoxic effect of TNF alpha (IC50 = 6 microM). The C-terminal region of this peptide, which is homologous to the 55 and 75 kDa TNF receptor, was found to be essential for activity.Entities:
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Year: 1994 PMID: 7935497 DOI: 10.1016/0161-5890(94)90101-5
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407