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Photoreactive stapled BH3 peptides to dissect the BCL-2 family interactome.


ABSTRACT: Defining protein interactions forms the basis for discovery of biological pathways, disease mechanisms, and opportunities for therapeutic intervention. To harness the robust binding affinity and selectivity of structured peptides for interactome discovery, we engineered photoreactive stapled BH3 peptide helices that covalently capture their physiologic BCL-2 family targets. The crosslinking ? helices covalently trap both static and dynamic protein interactors, and enable rapid identification of interaction sites, providing a critical link between interactome discovery and targeted drug design.

SUBMITTER: Braun CR 

PROVIDER: S-EPMC3048092 | biostudies-literature | 2010 Dec

REPOSITORIES: biostudies-literature

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Photoreactive stapled BH3 peptides to dissect the BCL-2 family interactome.

Braun Craig R CR   Mintseris Julian J   Gavathiotis Evripidis E   Bird Gregory H GH   Gygi Steven P SP   Walensky Loren D LD  

Chemistry & biology 20101201 12


Defining protein interactions forms the basis for discovery of biological pathways, disease mechanisms, and opportunities for therapeutic intervention. To harness the robust binding affinity and selectivity of structured peptides for interactome discovery, we engineered photoreactive stapled BH3 peptide helices that covalently capture their physiologic BCL-2 family targets. The crosslinking α helices covalently trap both static and dynamic protein interactors, and enable rapid identification of  ...[more]

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