Production of IgG1-based bispecific antibody without extra cysteine residue via intein-mediated protein trans-splicing

Sci Rep. 2021 Sep 30;11(1):19411. doi: 10.1038/s41598-021-98855-3.

Abstract

A major class of bispecific antibodies (BsAbs) utilizes heterodimeric Fc to produce the native immunoglobulin G (IgG) structure. Because appropriate pairing of heavy and light chains is required, the design of BsAbs produced through recombination or reassembly of two separately-expressed antigen-binding fragments is advantageous. One such method uses intein-mediated protein trans-splicing (IMPTS) to produce an IgG1-based structure. An extra Cys residue is incorporated as a consensus sequence for IMPTS in successful examples, but this may lead to potential destabilization or disturbance of the assay system. In this study, we designed a BsAb linked by IMPTS, without the extra Cys residue. A BsAb binding to both TNFR2 and CD30 was successfully produced. Cleaved side product formation was inevitable, but it was minimized under the optimized conditions. The fine-tuned design is suitable for the production of IgG-like BsAb with high symmetry between the two antigen-binding fragments that is advantageous for screening BsAbs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Bispecific / isolation & purification*
  • Humans
  • Immunoglobulin Fab Fragments / immunology*
  • Immunoglobulin G / immunology*
  • Protein Engineering / methods*
  • Recombinant Fusion Proteins / isolation & purification*

Substances

  • Antibodies, Bispecific
  • Immunoglobulin Fab Fragments
  • Immunoglobulin G
  • Recombinant Fusion Proteins