| Literature DB >> 19642697 |
Brett A Helms1, Sanne W A Reulen, Sebastiaan Nijhuis, Peggy T H M de Graaf-Heuvelmans, Maarten Merkx, E W Meijer.
Abstract
Peptides derived from phage display typically show significantly weaker binding than their respective high affinity phage, which can bind to protein surfaces in a multivalent fashion. Here we show that mimicking key aspects of the multivalent architecture of the phage on an AB(5) dendritic wedge can enhance the affinity of a phage-display derived collagen binding peptide 100-fold (K(d) = 550 nM), allowing direct visualization of collagen architectures in native tissues with a higher specificity than that of the native collagen binding protein CNA35. The dendrimer display approach introduced here represents a well-defined, highly versatile platform for the affinity enhancement of phage display-derived peptides that is likely to be broadly applicable.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19642697 DOI: 10.1021/ja902285m
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419