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Extensive research into the origin of cancer has led to the identification of genetic and molecular mistakes that trigger the overproduction or hyperactivity of specific cancer-causing proteins. The structural complexity and intracellular localization of these protein targets can hamper the development of pharmacologic tools to investigate and manipulate critical signaling networks in vivo. Peptide motifs within proteins serve as essential components of protein interaction surfaces, and are nature’s keys to cancer’s lock on cellular survival. Because natural peptides display evolutionarily honed binding specificity for their targets, synthetic peptides are uniquely poised to subvert cancer proteins. However, the ability to harness small peptides to block cancer has been hindered by their loss of natural architecture, vulnerability to degradation, and difficulty entering cells to exert their anti-tumor effects.

Hydrocarbon stapling recapitulates isolated peptide helices
Hydrocarbon stapling recapitulates isolated peptide helices

We are developing and applying new approaches to chemically stabilize natural peptides so that their shape, and therefore their anti-cancer activities can be restored. Optimizing natural peptides in this way provides alternative compounds to study protein interactions and manipulate biological pathways within cells to treat human disease. For example, we have used a chemical strategy, termed “hydrocarbon-stapling,” to synthesize a panel of pro-apoptotic peptides with markedly improved pharmacological properties. We have demonstrated that the stapled peptides retain their natural shape, are resistant to degradation, and can enter and kill leukemia cells by neutralizing their survival proteins. When administered to mice with leukemia, a stapled peptide modeled after the BH3 death domain of a BCL-2 family protein successfully blocked cancer growth and prolonged the lives of treated animals.

SAHBs can be used to modulate protein-protein interactions and influence subsequent pathways
SAHBs can be used to modulate protein-protein interactions and influence subsequent pathways

In ongoing studies, we broadly apply the new peptide-stapling strategy to produce a diversity of cancer biology discovery tools, in order to study and deactivate aberrant apoptotic and transcriptional pathways in a variety of human tumors.  We emphasize the structural basis for ligand-protein interactions, validation of intracellular targets, characterization of novel protein interactors, analysis of ligand-mediated alteration of signaling pathways in cellular and murine models of disease, in vivo imaging technologies, and clinical translation.

We employ numerous in vitro andin vivo assays to interrogate SAHB mechanism and therapeutic potential
We employ numerous in vitro and in vivo assays to interrogate SAHB mechanism and therapeutic potential