Title of article
An Improved Method for the Synthesis of Cellulose Membrane-Bound Peptides with Free C Termini Is Useful for PDZ Domain Binding Studies Original Research Article
Author/Authors
Prisca Boisguerin، نويسنده , , Rainer Leben، نويسنده , , Bernhard Ay، نويسنده , , Gerald Radziwill، نويسنده , , Karin Moelling، نويسنده , , Liying Dong، نويسنده , , Rudolf Volkmer-Engert، نويسنده ,
Issue Information
ماهنامه با شماره پیاپی سال 2004
Pages
11
From page
449
To page
459
Abstract
SPOT synthesis permits parallel synthesis and screening of thousands of cellulose membrane-bound peptides to study protein-protein interactions in a proteomic context. Recognition of C-terminal residues is one of the most common binding features of PDZ domains. Unfortunately, most solid support-bound peptide libraries lack a free C terminus due to C-terminal fixation on the solid support. To overcome this restriction, we developed a robust methodology based on our previous strategy for generating peptides with authentic C termini. To validate this improved method, we screened a human peptide library of 6223 C termini with the syntrophin PDZ domain. Furthermore, using the same library, new peptide ligands derived from membrane proteins and receptors were found for the ERBIN PDZ domain. Finally, we identified the protein kinase breakpoint cluster region, which is known as a negative regulator of cell proliferation and oncogenic transformation, as an ERBIN ligand.
Journal title
Chemistry and Biology
Serial Year
2004
Journal title
Chemistry and Biology
Record number
1158810
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