Improved variants of SrtA for site-specific conjugation on antibodies and proteins with high efficiency

Sci Rep. 2016 Aug 18:6:31899. doi: 10.1038/srep31899.

Abstract

Sortase mediated ligation is a highly specific platform for conjugation that relies on the specificity of the transpeptidase Sortase A (SrtA) for short peptide sequences (LPXTG and GGG). SrtA retains its specificity while accepting a wide range of potential substrates, but its broad use is limited by the wild-type enzyme's poor kinetics, which require large amounts of SrtA and extended reaction times for efficient conjugation. Prior explorations have aimed to improve the kinetics of SrtA with limited success. Herein we describe the discovery of further improved SrtA variants with increased efficiency for the conjugation reaction, and demonstrate their robustness in labelling proteins and antibodies in a site-specific manner. Our variants require significantly lower amounts of enzyme than WT SrtA and can be used to attach small molecules to the N or C-terminus of the heavy or light chain in antibodies with excellent yields. These improved variants can also be used for highly efficient site-specific PEGylation.

MeSH terms

  • Amino Acid Substitution
  • Aminoacyltransferases* / chemistry
  • Aminoacyltransferases* / genetics
  • Antibodies / chemistry*
  • Bacterial Proteins* / chemistry
  • Bacterial Proteins* / genetics
  • Cysteine Endopeptidases* / chemistry
  • Cysteine Endopeptidases* / genetics
  • Mutation, Missense*
  • Polyethylene Glycols / chemistry*
  • Staining and Labeling / methods*

Substances

  • Antibodies
  • Bacterial Proteins
  • Polyethylene Glycols
  • Aminoacyltransferases
  • sortase A
  • Cysteine Endopeptidases