Sodium dodecyl sulfate-polyacrylamide gel electrophoresis for screening nonaggregating human antibody heavy chain variable domains

Anal Biochem. 2010 Aug;403(1-2):117-9. doi: 10.1016/j.ab.2010.04.017. Epub 2010 Apr 18.

Abstract

Antibody heavy chain variable domains (V(H)s) form a significant class of biologics. With V(H) display libraries-the primary source of V(H) binders-unwanted aggregating V(H)s are coselected, sometimes overwhelmingly, alongside nonaggregating V(H)s. Thus, methods enabling efficient screening for nonaggregating V(H)s are highly valuable. Here, we found that on nonreducing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) gels, nonaggregating V(H)s migrate faster than expected, giving underestimated molecular weights (MWs), whereas aggregating ones migrate slower, giving overestimated MWs. Our finding can be applied to large-scale screening for nonaggregating V(H)s and possibly other proteins, in particular in display library settings, by SDS-PAGE.

MeSH terms

  • Electrophoresis, Polyacrylamide Gel / economics
  • Electrophoresis, Polyacrylamide Gel / methods*
  • High-Throughput Screening Assays / economics
  • High-Throughput Screening Assays / methods
  • Humans
  • Immunoglobulin Heavy Chains / chemistry*
  • Immunoglobulin Variable Region / chemistry*

Substances

  • Immunoglobulin Heavy Chains
  • Immunoglobulin Variable Region