Document Detail

Mapping discontinuous protein-binding sites via structure-based peptide libraries: combining in silico and in vitro approaches.
MedLine Citation:
PMID:  23280614     Owner:  NLM     Status:  In-Data-Review    
To perform their various functions, protein surfaces often have to interact with each other in a specific way. Usually, only parts of a protein are accessible and can act as binding sites. Because proteins consist of polypeptide chains that fold into complex three-dimensional shapes, binding sites can be divided into two different types: linear sites that follow the primary amino acid sequence and discontinuous binding sites, which are made up of short peptide fragments that are adjacent in spatial proximity. Such discontinuous binding sites dominate protein-protein interactions, but are difficult to identify. To meet this challenge, we combined a computational, structure-based approach and an experimental, high-throughput method. SUPERFICIAL is a program that uses protein structures as input and generates peptide libraries to represent the protein's surface. A large number of the predicted peptides can be simultaneously synthesised applying the SPOT technology. The results of a binding assay subsequently help to elucidate protein-protein interactions; the approach is applicable to any kind of protein. The crystal structure of the complex of hen egg lysozyme with the well-characterised murine IgG1 antibody HyHEL-5 is available, and the complex is known to have a discontinuous binding site. Using SUPERFICIAL, the entire surface of lysozyme was translated into a peptide library that was synthesised on a cellulose membrane using the SPOT technology and tested against the HyHEL-5 antibody. In this way, it was possible to identify two peptides (longest common sequence and peptide 19) that represented the discontinuous epitope of lysozyme. Copyright © 2012 John Wiley & Sons, Ltd.
Ines S Jaeger; Ines Kretzschmar; Jana Körner; Armin A Weiser; Carsten C Mahrenholz; Ajish Potty; Katerina Kourentzi; Richard C Willson; Rudolf Volkmer; Robert Preissner
Related Documents :
23082934 - Evaluation of database search programs for accurate detection of neuropeptides in tande...
23902564 - Classification and assessment tools for structural motif discovery algorithms.
24689774 - Identification of conformational antigenic epitopes and dominant amino acids of buffalo...
9115414 - Mechanism of alkaloid cyclopeptide synthesis in the ergot fungus claviceps purpurea.
1137984 - Electrophoretic separation of tubulin alpha and beta subunits after s-sulfonation.
2036404 - Structure of the membrane-bound protein photosynthetic reaction center from rhodobacter...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Journal of molecular recognition : JMR     Volume:  26     ISSN:  1099-1352     ISO Abbreviation:  J. Mol. Recognit.     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-01-02     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9004580     Medline TA:  J Mol Recognit     Country:  England    
Other Details:
Languages:  eng     Pagination:  23-31     Citation Subset:  IM    
Copyright Information:
Copyright © 2012 John Wiley & Sons, Ltd.
Institute for Physiology, Structural Bioinformatics Group, Charité-Universitätsmedizin Berlin, Lindenberger Weg 80, 13125, Berlin, Germany.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Effect of CoCl(2) on the content of different metals and a relative activity of DNA-hydrolyzing abz...
Next Document:  Glutathione S-transferase ? complexes with and stimulates Na(+) ,K(+) -ATPase.