Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1373214 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
A series of multivalent peptides, with the ability to simultaneously bind two separate PDZ domain proteins, has been designed, synthesized, and tested by isothermal titration calorimetry (ITC). The monomer sequences, linked with succinate, varied in length from five to nine residues. The thermodynamic binding parameters, in conjunction with results from mass spectrometry, indicate that a ternary complex is formed in which each peptide arm binds two equivalents of the third PDZ domain (PDZ3) of the neuronal protein PSD-95.
Graphical abstractThe design, synthesis, and thermodynamic binding evaluation of homobivalent peptides capable of binding two PDZ domain proteins is presented.Figure optionsDownload full-size imageDownload as PowerPoint slide