Antibody Engineering

pp 85-99


  • Jonas V. SchaeferAffiliated withBiochemisches Institut, Universität Zürich
  • , Peter LindnerAffiliated withBiochemisches Institut, Universität Zürich
  • , Andreas PlückthunAffiliated withBiochemisches Institut, Universität Zürich Email author 

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Recombinant antibodies have become a standard component of research, diagnostics, and therapy. In the development of recombinant antibodies – irrespective of the final format – a monovalent construct is virtually always the first protein to be tested. This is due to the fact that essentially all selection systems use such formats, and that the periplasmic production of scFv and Fab fragments has now become standard. Nonetheless, some tasks require an increase of the avidity to the respective antigens, antibody, as well as the fragment size. A convenient way to rather quickly achieve both is by fusing a hinge region followed by a dimerizing or oligomerizing structure to the C-terminus of the antibody fragment, creating the so-called “miniantibodies”. Compared to other available bivalent or bispecific formats, miniantibodies distinguish themselves by their rotational freedom and flexibility, being similar to full-length antibodies. This protocol describes the modular conversion of scFv fragments into miniantibodies, resulting in a final multimerized structure with two or four binding sites, and we present different self-associating domains suitable for this task. Additionally, we also provide information on their production and discuss how to improve the yield of soluble antibody fragments.