Literature DB >> 16321044

An immobilized biotin ligase: surface display of Escherichia coli BirA on Saccharomyces cerevisiae.

Ranganath Parthasarathy1, Jitin Bajaj, Eric T Boder.   

Abstract

The Escherichia coli biotin ligase enzyme BirA has been extensively used in recent years to generate site-specifically biotinylated proteins via a biotin acceptor peptide tag. In the present study, BirA was displayed for the first time on the yeast Saccharomyces cerevisiae using the Aga1p-Aga2p platform and assayed using a peptide-tagged protein as the substrate. The enzyme is fully functional and resembles the soluble form in many of its properties, but the yeast-displayed enzyme demonstrates stability and reusability on the time scale of weeks. Thus, the yeast-displayed BirA system represents a facile and highly economical alternative for producing site-specifically biotinylated proteins.

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Year:  2005        PMID: 16321044     DOI: 10.1021/bp050279t

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  6 in total

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3.  Kinetic Competition Screening of Yeast-Displayed Libraries for Isolating High Affinity Binders.

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Journal:  Methods Mol Biol       Date:  2022

4.  High-throughput biotinylation of proteins.

Authors:  Brian K Kay; Sang Thai; Veronica V Volgina
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5.  Facile chemical functionalization of proteins through intein-linked yeast display.

Authors:  Carrie J Marshall; Nitin Agarwal; Jeet Kalia; Vanessa A Grosskopf; Nicholas A McGrath; Nicholas L Abbott; Ronald T Raines; Eric V Shusta
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Review 6.  Yeast surface display for protein engineering and characterization.

Authors:  S Annie Gai; K Dane Wittrup
Journal:  Curr Opin Struct Biol       Date:  2007-09-17       Impact factor: 6.809

  6 in total

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