Engineering Allostery into Proteins

Adv Exp Med Biol. 2019:1163:359-384. doi: 10.1007/978-981-13-8719-7_15.

Abstract

Our ability to engineer protein structure and function has grown dramatically over recent years. Perhaps the next level in protein design is to develop proteins whose function can be regulated in response to various stimuli, including ligand binding, pH changes, and light. Endeavors toward these goals have tested and expanded on our understanding of protein function and allosteric regulation. In this chapter, we provide examples from different methods for developing new allosterically regulated proteins. These methods range from whole insertion of regulatory domains into new host proteins, to covalent attachment of photoswitches to generate light-responsive proteins, and to targeted changes to specific amino acid residues, especially to residues identified to be important for relaying allosteric information across the protein framework. Many of the examples we discuss have already found practical use in medical and biotechnology applications.

Keywords: Allostery; Amino acid network; Covalent modification; Domain insertion; Energy landscape; Protein engineering; Protein regulation.

Publication types

  • Review

MeSH terms

  • Allosteric Regulation
  • Mutagenesis, Site-Directed
  • Protein Engineering* / methods
  • Protein Engineering* / trends
  • Proteins* / chemistry

Substances

  • Proteins