The human combinatorial antibody library HuCAL GOLD combines diversification of all six CDRs according to the natural immune system with a novel display method for efficient selection of high-affinity antibodies |
| |
Authors: | Rothe Christine Urlinger Stefanie Löhning Corinna Prassler Josef Stark Yvonne Jäger Ute Hubner Bernd Bardroff Michael Pradel Ingrid Boss Melanie Bittlingmaier Renate Bataa Tschimegma Frisch Christian Brocks Bodo Honegger Annemarie Urban Margit |
| |
Affiliation: | 1 MorphoSys AG, Lena-Christ-Strasse 48, 82152 Martinsried, Germany 2 Sandoz Biopharmaceuticals, Hexal Biotech Forschungs GmbH, Keltenring 1+3, 82041 Oberhaching, Germany 3 Department of Pediatric Oncology, Hematology and Immunology, University of Düsseldorf, Germany 4 Institute of Tropical Medicine and Parasitology, Leopoldstrasse 5, 80802 Munich, Germany 5 Institute of Biochemistry, Medical Faculty, Christian Albrecht University Kiel, Otto-Hahn-Platz 9, 24118 Kiel, Germany 6 AbD Serotec, A Division of MorphoSys, Lena-Christ-Strasse 48, 82152 Martinsried, Germany 7 Department of Biochemistry, University of Zurich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland |
| |
Abstract: | This article describes the generation of the Human Combinatorial Antibody Library HuCAL GOLD. HuCAL GOLD is a synthetic human Fab library based on the HuCAL concept with all six complementarity-determining regions (CDRs) diversified according to the sequence and length variability of naturally rearranged human antibodies. The human antibody repertoire was analyzed in-depth, and individual CDR libraries were designed and generated for each CDR and each antibody family. Trinucleotide mixtures were used to synthesize the CDR libraries in order to ensure a high quality within HuCAL GOLD, and a β-lactamase selection system was employed to eliminate frame-shifted clones after successive cloning of the CDR libraries. With these methods, a large, high-quality library with more than 10 billion functional Fab fragments was achieved. By using CysDisplay, the antibody fragments are displayed on the tip of the phage via a disulfide bridge between the phage coat protein pIII and the heavy chain of the antibody fragment. Efficient elution of specific phages is possible by adding reducing agents. HuCAL GOLD was challenged with a variety of different antigens and proved to be a reliable source of high-affinity human antibodies with best affinities in the picomolar range, thus functioning as an excellent source of antibodies for research, diagnostic, and therapeutic applications. Furthermore, the data presented in this article demonstrate that CysDisplay is a robust and broadly applicable display technology even for high-throughput applications. |
| |
Keywords: | CDR, complementarity-determining region VH domain, heavy-chain variable domain VL domain, light-chain variable domain Fd fragment, heavy-chain fragment consisting of a VH and a CH1 domain HuCAL, Human Combinatorial Antibody Library LCDR, light-chain complementarity-determining region HCDR, heavy-chain complementarity-determining region IL18R-Fc, Fc-conjugated interleukin-18 receptor β-Gal, β-galactosidase Est-BSA, β-estradiol coupled to bovine serum albumin PDB, Protein Data Bank Cm, chloramphenicol Glu, glucose PBS, phosphate-buffered saline |
本文献已被 ScienceDirect PubMed 等数据库收录! |
|