Structure-Based Redesign of the Binding Specificity of Anti-Apoptotic Bcl-x[subscript L]

Many native proteins are multi-specific and interact with numerous partners, which can confound analysis of their functions. Protein design provides a potential route to generating synthetic variants of native proteins with more selective binding profiles. Redesigned proteins could be used as resear...

Full description

Bibliographic Details
Main Authors: Chen, T. Scott (Contributor), Palacios, Hector (Contributor), Keating, Amy E. (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Biology (Contributor)
Format: Article
Language:English
Published: Elsevier, 2016-02-25T03:18:14Z.
Subjects:
Online Access:Get fulltext
LEADER 02509 am a22002293u 4500
001 101270
042 |a dc 
100 1 0 |a Chen, T. Scott  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Biology  |e contributor 
100 1 0 |a Chen, T. Scott  |e contributor 
100 1 0 |a Palacios, Hector  |e contributor 
100 1 0 |a Keating, Amy E.  |e contributor 
700 1 0 |a Palacios, Hector  |e author 
700 1 0 |a Keating, Amy E.  |e author 
245 0 0 |a Structure-Based Redesign of the Binding Specificity of Anti-Apoptotic Bcl-x[subscript L] 
260 |b Elsevier,   |c 2016-02-25T03:18:14Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/101270 
520 |a Many native proteins are multi-specific and interact with numerous partners, which can confound analysis of their functions. Protein design provides a potential route to generating synthetic variants of native proteins with more selective binding profiles. Redesigned proteins could be used as research tools, diagnostics or therapeutics. In this work, we used a library screening approach to reengineer the multi-specific anti-apoptotic protein Bcl-x[subscript L] to remove its interactions with many of its binding partners, making it a high-affinity and selective binder of the BH3 region of pro-apoptotic protein Bad. To overcome the enormity of the potential Bcl-x[subscript L] sequence space, we developed and applied a computational/experimental framework that used protein structure information to generate focused combinatorial libraries. Sequence features were identified using structure-based modeling, and an optimization algorithm based on integer programming was used to select degenerate codons that maximally covered these features. A constraint on library size was used to ensure thorough sampling. Using yeast surface display to screen a designed library of Bcl-x[subscript L] variants, we successfully identified a protein with ~ 1000-fold improvement in binding specificity for the BH3 region of Bad over the BH3 region of Bim. Although negative design was targeted only against the BH3 region of Bim, the best redesigned protein was globally specific against binding to 10 other peptides corresponding to native BH3 motifs. Our design framework demonstrates an efficient route to highly specific protein binders and may readily be adapted for application to other design problems. 
520 |a National Institutes of Health (U.S.) (Award GM084181) 
546 |a en_US 
655 7 |a Article 
773 |t Journal of Molecular Biology