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. 1997 Dec 15;25(24):5132-4.
doi: 10.1093/nar/25.24.5132.

Antibody-ribosome-mRNA (ARM) complexes as efficient selection particles for in vitro display and evolution of antibody combining sites

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Antibody-ribosome-mRNA (ARM) complexes as efficient selection particles for in vitro display and evolution of antibody combining sites

M He et al. Nucleic Acids Res. .

Abstract

We describe a rapid, eukaryotic, in vitro method for selection and evolution of antibody combining sites using antibody-ribosome-mRNA (ARM) complexes as selection particles. ARMs carrying single-chain (VH/K) binding fragments specific for progesterone were selected using antigen-coupled magnetic beads; selection simultaneously captured the genetic information as mRNA, making it possible to generate and amplify cDNA by single-step RT-PCR on the ribosome-bound mRNA for further manipulation. Using mutant libraries, antigen-binding ARMs were enriched by a factor of 10(4)-10(5)-fold in a single cycle, with further enrichment in repeated cycles. While demonstrated here for antibodies, the method has the potential to be applied equally for selection of receptors or peptides from libraries.

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References

    1. Biotechniques. 1990 Apr;8(4):404-7 - PubMed
    1. J Cell Biol. 1991 Apr;113(1):35-44 - PubMed
    1. Trends Biotechnol. 1993 Jan;11(1):6-10 - PubMed
    1. J Biol Chem. 1993 Mar 5;268(7):5302-8 - PubMed
    1. J Mol Biol. 1993 May 5;231(1):103-18 - PubMed

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