Literature DB >> 7935497

Identification and characterization of a TNF alpha antagonist derived from a monoclonal antibody.

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.

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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


  2 in total

Review 1.  Structure-based design of immunologically active therapeutic peptides.

Authors:  R Murali; M I Greene
Journal:  Immunol Res       Date:  1998       Impact factor: 2.829

2.  Structure-Based Design, Synthesis and Bioactivity of a New Anti-TNFα Cyclopeptide.

Authors:  Mohannad Idress; Bruce F Milne; Gary S Thompson; Laurent Trembleau; Marcel Jaspars; Wael E Houssen
Journal:  Molecules       Date:  2020-02-19       Impact factor: 4.927

  2 in total

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