Leveraging SBDD in protein therapeutic development: antibody engineering

Methods Mol Biol. 2012:841:321-49. doi: 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.

Publication types

  • Review

MeSH terms

  • Antibodies / chemistry
  • Antibodies / therapeutic use*
  • Crystallography, X-Ray
  • Drug Design*
  • Humans
  • Models, Molecular
  • Molecular Structure
  • Protein Engineering*

Substances

  • Antibodies