Affinity maturation of antibody fragments: A review encompassing the development from random approaches to computational rational optimization

Int J Biol Macromol. 2023 Aug 30:247:125733. doi: 10.1016/j.ijbiomac.2023.125733. Epub 2023 Jul 7.

Abstract

Routinely screened antibody fragments usually require further in vitro maturation to achieve the desired biophysical properties. Blind in vitro strategies can produce improved ligands by introducing random mutations into the original sequences and selecting the resulting clones under more and more stringent conditions. Rational approaches exploit an alternative perspective that aims first at identifying the specific residues potentially involved in the control of biophysical mechanisms, such as affinity or stability, and then to evaluate what mutations could improve those characteristics. The understanding of the antigen-antibody interactions is instrumental to develop this process the reliability of which, consequently, strongly depends on the quality and completeness of the structural information. Recently, methods based on deep learning approaches critically improved the speed and accuracy of model building and are promising tools for accelerating the docking step. Here, we review the features of the available bioinformatic instruments and analyze the reports illustrating the result obtained with their application to optimize antibody fragments, and nanobodies in particular. Finally, the emerging trends and open questions are summarized.

Keywords: deep learning; protein modeling; random mutagenesis; rational mutagenesis.

Publication types

  • Review

MeSH terms

  • Antibodies* / genetics
  • Antibody Affinity
  • Immunoglobulin Fragments*
  • Mutation
  • Reproducibility of Results

Substances

  • Immunoglobulin Fragments
  • Antibodies