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Application of constrained aza-valine analogs for Smac mimicry.
- Source :
-
Biopolymers [Biopolymers] 2016 May; Vol. 106 (3), pp. 235-44. - Publication Year :
- 2016
-
Abstract
- Constrained azapeptides were designed based on the Ala-Val-Pro-Ile sequence from the second mitochondria-derived activator of caspases (Smac) protein and tested for ability to induce apoptosis in cancer cells. Diels-Alder cyclizations and Alder-ene reactions on azopeptides enabled construction of a set of constrained aza-valine dipeptide building blocks, that were introduced into mimics using effective coupling conditions to acylate bulky semicarbazide residues. Evaluation of azapeptides 7-11 in MCF-7 breast cancer cells indicated aza-cyclohexanylglycyine analog 11 induced cell death more efficiently than the parent tetrapeptide likely by a caspase-9 mediated apoptotic pathway. © 2016 Wiley Periodicals, Inc. Biopolymers (Pept Sci) 106: 235-244, 2016.<br /> (© 2016 Wiley Periodicals, Inc.)
- Subjects :
- Acylation
Amino Acid Motifs
Antineoplastic Agents pharmacology
Apoptosis drug effects
Apoptosis Regulatory Proteins
Aza Compounds pharmacology
Caspase 9 genetics
Caspase 9 metabolism
Cell Survival drug effects
Cyclization
Dose-Response Relationship, Drug
Gene Expression
Humans
Inhibitor of Apoptosis Proteins genetics
Inhibitor of Apoptosis Proteins metabolism
Intracellular Signaling Peptides and Proteins genetics
Intracellular Signaling Peptides and Proteins metabolism
MCF-7 Cells
Mitochondrial Proteins genetics
Mitochondrial Proteins metabolism
Molecular Mimicry
Peptides pharmacology
Protein Binding
Semicarbazides chemistry
Antineoplastic Agents chemical synthesis
Aza Compounds chemical synthesis
Inhibitor of Apoptosis Proteins antagonists & inhibitors
Intracellular Signaling Peptides and Proteins chemistry
Mitochondrial Proteins chemistry
Peptides chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1097-0282
- Volume :
- 106
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biopolymers
- Publication Type :
- Academic Journal
- Accession number :
- 27087660
- Full Text :
- https://doi.org/10.1002/bip.22851