Leveraging SBDD in Protein Therapeutic Development: Antibody Engineering
- 7 December 2011
- book chapter
- Published by Springer Nature
- Vol. 841, 321-349
- https://doi.org/10.1007/978-1-61779-520-6_14
Abstract
Antibodies make up the largest, growing segment of protein therapeutics in the pharmaceutical and biotechnology industries. The development or engineering of therapeutic antibodies is based to a large extent on our knowledge of antibody structure and requires sophisticated methods that continue to evolve. In this chapter, after a review of what is known about the structure and functional properties of antibodies, the current, state-of-the-art antibody engineering methods are described. These methods include antibody humanization, antigen-affinity optimization, Fc engineering for modulated effector function and extended half-life, and engineering for improved stability and biophysical properties. X-ray crystallographic structures of antibody fragments and their complexes can play a critical role in guiding and, in some cases, accelerating these processes. These approaches represent guidelines for developing antibody therapeutics with the desired affinity, effector function, and biophysical properties.Keywords
This publication has 142 references indexed in Scilit:
- A New Clustering of Antibody CDR Loop ConformationsPublished by Elsevier ,2010
- Coevolution of Antibody Stability and Vκ CDR-L3 Canonical StructureJournal of Molecular Biology, 2010
- Human Framework Adaptation of a Mouse Anti-Human IL-13 AntibodyJournal of Molecular Biology, 2010
- Engineering Fully Human Monoclonal Antibodies from Murine Variable RegionsJournal of Molecular Biology, 2010
- Improving the solubility of anti‐LINGO‐1 monoclonal antibody Li33 by isotype switching and targeted mutagenesisProtein Science, 2010
- Structure and function of immunoglobulinsJournal of Allergy and Clinical Immunology, 2010
- De Novo Selection of High-Affinity Antibodies from Synthetic Fab Libraries Displayed on Phage as pIX Fusion ProteinsJournal of Molecular Biology, 2010
- Methionine oxidation in human IgG2 Fc decreases binding affinities to protein A and FcRnProtein Science, 2009
- Toward high‐resolution homology modeling of antibody Fv regions and application to antibody–antigen dockingProteins-Structure Function and Bioinformatics, 2008
- 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 AntibodiesJournal of Molecular Biology, 2007