Selective targeting of a laccase from Stachybotrys chartarum covalently linked to a carotenoid-binding peptide

:  A two‐step targeting strategy was used to identify improved laccases for bleaching carotenoid‐containing stains on fabric. We first applied a modified phage display technique to identify peptide sequences capable of binding specifically to carotenoid stains and not to fabric. Prior deselection on...

Full description

Saved in:
Bibliographic Details
Published in:The journal of peptide research Vol. 64; no. 1; pp. 10 - 24
Main Authors: Janssen, G.G., Baldwin, T.M., Winetzky, D.S., Tierney, L.M., Wang, H., Murray, C.J.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-07-2004
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary::  A two‐step targeting strategy was used to identify improved laccases for bleaching carotenoid‐containing stains on fabric. We first applied a modified phage display technique to identify peptide sequences capable of binding specifically to carotenoid stains and not to fabric. Prior deselection on the support on which the carotenoid was localized, increased stringency during the biopanning target selection process, and analysis of the phage peptides’ binding to the target after acid elution and polymerase chain reaction (PCR) postacid elution, were used to isolate phage peptide libraries with increased binding selectivity and affinity. Peptide sequences were selected based on identified consensus motifs. We verified the enhanced carotenoid‐binding properties of the peptide YGYLPSR and subsequently cloned and expressed C‐terminal variants of laccase from Stachybotrys chartarum containing carotenoid‐binding peptides YGYLPSR, IERSAPATAPPP, KASAPAL, CKASAPALC, and SLLNATK. These targeted peptide–laccase fusions demonstrate enhanced catalytic properties on stained fabrics.
Bibliography:ark:/67375/WNG-MH0CFF12-W
istex:2BFDC52DD09908FA07701ADE48A91CD6A292BB67
ArticleID:CBDD150
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1397-002X
1399-3011
DOI:10.1111/j.1399-3011.2004.00150.x