Molecular Biotechnology

, Volume 24, Issue 1, pp 1–9 | Cite as

Efficient display of two enzymes on filamentous phage using an improved signal sequence

Research

Abstract

Directed protein-evolution strategies generally make use of a link between a protein and the encoding DNA. In phage-display technology, this link is provided by fusion of the protein with a coat protein that is incorporated into the phage particle containing the DNA. Optimization of this link can be achieved by adjusting the signal sequence of the fusion. In a previous study, directed evolution of signal sequences for optimal display of the Taq DNA polymerase I Stoffel fragment on phage yielded signal peptides with a 50-fold higher incorporation of fusion proteins in phage particles. In this article, we show that for one of the selected signal sequences, improved display on phage can be generalized to other proteins, such as adenylate cyclases from Escherichia coli and Bordetella pertussis, and that this is highly dependent on short sequences at the C-terminus of the signal peptide. Further, the display of two enzymes on phage has been achieved and may provide a strategy for directing coevolution of the two proteins. These findings should be useful for display of large and cytoplasmic proteins on filamentous phage.

Index Entries

Signal peptide leader phagemid adenylate cyclase Stoffel fragment phage display 

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Copyright information

© Humana Press Inc 2003

Authors and Affiliations

  1. 1.Unité de Chimie Organique, CNRS URA 2185, Département de Biologie Structurale et ChimieInstitut PasteurParisFrance

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