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Biochem Biophys Res Commun. 2012 Nov 23;428(3):395-400. doi: 10.1016/j.bbrc.2012.10.066. Epub 2012 Oct 26.

Robust in vitro affinity maturation strategy based on interface-focused high-throughput mutational scanning.

Author information

1
Advanced Medical Research Department, Mitsubishi Tanabe Pharma Corporation, 3-16-89 Kashima, Osaka 532-8505, Japan. Fujino.Yasuhiro@mb.mt-pharma.co.jp

Abstract

Development of protein therapeutics or biosensors often requires in vitro affinity maturation. Here we report a robust affinity engineering strategy using a custom designed library. The strategy consists of two steps beginning with identification of beneficial single amino acid substitutions then combination. A high quality combinatorial library specifically customized to a given binding-interface can be rapidly designed by high-throughput mutational scanning of single substitution libraries. When applied to the optimization of a model antibody Fab fragment, the strategy created a diverse panel of high affinity variants. The most potent variant achieved 2110-fold affinity improvement to an equilibrium dissociation constant (Kd) of 3.45 pM with only 7 amino acid substitutions. The method should facilitate affinity engineering of a wide variety of protein-protein interactions due to its context-dependent library design strategy.

PMID:
23103372
DOI:
10.1016/j.bbrc.2012.10.066
[Indexed for MEDLINE]
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