4.2 Article

Selecting for antibody scFv fragments with improved stability using phage display with denaturation under reducing conditions

Journal

JOURNAL OF IMMUNOLOGICAL METHODS
Volume 296, Issue 1-2, Pages 159-170

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jim.2004.11.008

Keywords

antibody engineering; disulfide bond; phage display; protein denaturation; protein stability

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Stability of single-chain Fvs (scFvs) can be improved by mutagenesis followed by phage display selection where the unstable variants are first inactivated by, for example, denaturing treatment. Here we describe a modified strategy for the selection of stabilized antibody fragments by phage display, based on denaturation under reducing conditions. This strategy was applied to an anti-thyroid-stimulating hormone (TSH) scFv fragment which refolded remarkably during the selection if denaturation was carried out in conventionally used non-reducing conditions. Refolding was, however, efficiently prevented by combining denaturation with reduction of the intra-domain disulfide bridges, which created favourable conditions for selection of clones with improved stability. Using this strategy, scFv mutants with 8-9 degreesC improved thermal stability and 0.8-0.9 M improved stability for guanidinium chloride were found after 4-5 enrichment cycles. The most stable mutants selected contained either Lys(H)66Arg or Asn(H)52aSer mutations, which are known to stabilize other scFvs. Periplasmic expression level of the mutants was also improved. (C) 2004 Elsevier B.V. All rights reserved.

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