TY  - UNPB
ID  - pittir9524
UR  - http://d-scholarship-dev.library.pitt.edu/9524/
A1  - Brown, Zachary Z
TI  - Synthesis and Application of Functionalized Bis-Peptides Through Hindered Amide Bond Formation
Y1  - 2011/01/30/
N2  - This work presents significant advances towards installing chemical functionality within bis-peptide scaffolds, an important milestone towards designer, functional macromolecules for our group. First was the discovery of acyl-transfer coupling, a new synthetic route to assemble extremely hindered peptide bonds which were not previously accessible through conventional means. A novel amino-anhydride intermediate and five-membered ring acyl-transfer mechanism is postulated and multiple supporting pieces of evidence are presented. Applying this chemistry to the bis-amino acid building blocks developed in our group, the first functionalized bis-peptides were created which are oligomeric, diketopiperazine-based peptidomimetics. The first application for this new class of macromolecules was to mimic the bound conformation of the p53 ?Ñ-helical domain to its binding partner hDM2. Further structure and function optimization and characterization of the compound¡¦s biological effects showed these bis-peptides to be potent inhibitors of this protein-protein interaction, be cell-permeable and elicit a surprising biological response with human liver cancer cells.
AV  - public
KW  - Amide Bond Formation; Bis-Peptides; Peptide Chemistry; Peptidomimietics
ER  -