Design of pH sensitive binding proteins from the hyperthermophilic Sso7d scaffold

PLoS One. 2012;7(11):e48928. doi: 10.1371/journal.pone.0048928. Epub 2012 Nov 7.

Abstract

We have engineered pH sensitive binding proteins for the Fc portion of human immunoglobulin G (hIgG) (hFc) using two different strategies - histidine scanning and random mutagenesis. We obtained an hFc-binding protein, Sso7d-hFc, through mutagenesis of the Sso7d protein from the hyperthermophilic archaeon Sulfolobus solfataricus; Sso7d-hFc was isolated from a combinatorial library of Sso7d mutants using yeast surface display. Subsequently, we identified a pH sensitive mutant, Sso7d-his-hFc, through systematic evaluation of Sso7d-hFc mutants containing single histidine substitutions. In parallel, we also developed a yeast display screening strategy to isolate a different pH sensitive hFc binder, Sso7d-ev-hFc, from a library of mutants obtained by random mutagenesis of a pool of hFc binders. In contrast to Sso7d-hFc, both Sso7d-his-hFc and Sso7d-ev-hFc have a higher binding affinity for hFc at pH 7.4 than at pH 4.5. The Sso7d-mutant hFc binders can be recombinantly expressed at high yield in E. coli and are monomeric in solution. They bind an epitope in the CH3 domain of hFc that has high sequence homology in all four hIgG isotypes (hIgG(1-4)), and recognize hIgG(1-4) as well as deglycosylated hIgG in western blotting assays. pH sensitive hFc binders are attractive candidates for use in chromatography, to achieve elution of IgG under milder pH conditions. However, the surface density of immobilized hFc binders, as well as the avidity effect arising from the multivalent interaction of dimeric hFc with the capture surface, influences the pH dependence of dissociation from the capture surface. Therefore, further studies are needed to evaluate if the Sso7d mutants identified in this study are indeed useful as affinity ligands in chromatography.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Epitopes / genetics
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Histidine / genetics
  • Histidine / metabolism
  • Humans
  • Hydrogen-Ion Concentration
  • Immunoglobulin Fc Fragments / genetics
  • Immunoglobulin Fc Fragments / metabolism*
  • Immunoglobulin G / genetics
  • Immunoglobulin G / metabolism*
  • Mutagenesis
  • Sulfolobus solfataricus / genetics
  • Sulfolobus solfataricus / metabolism*

Substances

  • Carrier Proteins
  • Epitopes
  • Immunoglobulin Fc Fragments
  • Immunoglobulin G
  • Histidine

Grant support

This work was supported by grants from the National Science Foundation (NSF; grant CBET-0853771) and the Defense Threat Reduction Agency (DTRA; grant HDTRA1-10-1-0024). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.