Rationale for Bcl-xL/Bad peptide complex formation from structure, mutagenesis, and biophysical studies

AM Petros, DG Nettesheim, Y Wang, ET Olejniczak… - Protein …, 2000 - cambridge.org
AM Petros, DG Nettesheim, Y Wang, ET Olejniczak, RP Meadows, J Mack, K Swift…
Protein Science, 2000cambridge.org
The three-dimensional structure of the anti-apoptotic protein Bcl-xL complexed to a 25-
residue peptide from the death promoting region of Bad was determined using NMR
spectroscopy. Although the overall structure is similar to Bcl-xL bound to a 16-residue
peptide from the Bak protein (Sattler et al., 1997), the Bad peptide forms additional
interactions with Bcl-xL. However, based upon site-directed mutagenesis experiments, these
additional contacts do not account for the increased affinity of the Bad 25-mer for Bcl-xL …
The three-dimensional structure of the anti-apoptotic protein Bcl-xL complexed to a 25-residue peptide from the death promoting region of Bad was determined using NMR spectroscopy. Although the overall structure is similar to Bcl-xL bound to a 16-residue peptide from the Bak protein (Sattler et al., 1997), the Bad peptide forms additional interactions with Bcl-xL. However, based upon site-directed mutagenesis experiments, these additional contacts do not account for the increased affinity of the Bad 25-mer for Bcl-xL compared to the Bad 16-mer. Rather, the increased helix propensity of the Bad 25-mer is primarily responsible for its greater affinity for Bcl-xL. Based on this observation, a pair of 16-residue peptides were designed and synthesized that were predicted to have a high helix propensity while maintaining the interactions important for complexation with Bcl-xL. Both peptides showed an increase in helix propensity compared to the wild-type and exhibited an enhanced affinity for Bcl-xL.
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