Literature DB >> 12628249

Design of a modular immunotoxin connected by polyionic adapter peptides.

Martin Kleinschmidt1, Rainer Rudolph, Hauke Lilie.   

Abstract

Immunotoxins are genetically engineered fusion proteins of an antibody Fv fragment and a toxin from bacteria or plants, which function as anti-cancer therapeutics. Here, we describe a new generation of immunotoxins in which both proteins do not form a single fusion protein but are coupled specifically via cysteine-containing polyionic fusion peptides. The engineered Pseudomonas exotoxin PE38 was N-terminally fused to the peptide E(8)C. In combination with the disulfide-stabilized Fv fragment of the tumor-specific antibody B3, which was extended by the peptide R(8)CP, the fusion peptides ensured a specific and covalent coupling of the Fv fragment and the toxin. The resulting immunotoxin was as active and as specific as an immunotoxin consisting of a fusion protein of the same antibody fragment connected to the toxin.

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Year:  2003        PMID: 12628249     DOI: 10.1016/s0022-2836(03)00141-4

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   6.151


  2 in total

1.  Listeriolysin O as cytotoxic component of an immunotoxin.

Authors:  Sabine Bergelt; Stefan Frost; Hauke Lilie
Journal:  Protein Sci       Date:  2009-06       Impact factor: 6.725

2.  Bispecific antibody derivatives with restricted binding functionalities that are activated by proteolytic processing.

Authors:  Silke Metz; Christian Panke; Alexander K Haas; Jürgen Schanzer; Wilma Lau; Rebecca Croasdale; Eike Hoffmann; Britta Schneider; Johannes Auer; Christian Gassner; Birgit Bossenmaier; Pablo Umana; Claudio Sustmann; Ulrich Brinkmann
Journal:  Protein Eng Des Sel       Date:  2012-09-13       Impact factor: 1.650

  2 in total

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