The goal of this proposal is to predict and design specific protein interactions by using a combination of computational and experimental methods. To reduce the complexity of the problem, we target interactions mediated by the coiled coil. The coiled coil is a simple and important interaction motif estimated to occur in roughly 3-5% of all proteins, including many important for human disease. It has been studied extensively over the past 15 years. Consequently, existing knowledge provides a framework in which to attempt the challenging problems of interaction prediction and design.
The specific aims of the proposal are: (1) To measure the pairings that occur among coiled coils found in human and yeast bZIP transcription factors. This will be accomplished using a large-scale protein microarray assay. The resulting data will be used to develop computational methods for predicting coiled-coil interactions from sequence. The bZIP interaction screen will also provide a wealth of data for the study of transcriptional regulatory networks that involve human oncogenes, including Fos and Jun. (2) To improve computational methods that have been developed for protein design so that these are more suitable for the problem of designing interaction specificity. 3) To use computationally-guided methods from Aim 2 to design peptides that bind specifically to targeted human bZIP coiled-coil domains, and to test these designs experimentally. This will provide a comparison of designed peptides with naturally occurring ones (Aim 1) that share similar interaction properties. It will also constitute a rigorous test of our basic understanding of coiled-coil recognition, and it will provide useful reagents for perturbing transcriptional regulatory networks. (4) To design a peptide that acts as an inhibitor of the oligomerization of BcrAbl, a human oncoprotein. The coiled coil-mediated dimerization of Bcr is implicated in more than 95% of chronic myelogenous leukemias. Together, these studies will improve our understanding of the molecular basis of protein interaction specificity and provide tools that can be used to rationally alter protein structure and function. The methods proposed can be applied to a wide range of different domain-domain interactions, so the insights that we achieve will have broad significance for the study of protein-protein associations generally.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM067681-02
Application #
6844778
Study Section
Molecular and Cellular Biophysics Study Section (BBCA)
Program Officer
Basavappa, Ravi
Project Start
2004-02-01
Project End
2009-01-31
Budget Start
2005-02-01
Budget End
2006-01-31
Support Year
2
Fiscal Year
2005
Total Cost
$280,589
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Rezaei Araghi, Raheleh; Keating, Amy E (2016) Designing helical peptide inhibitors of protein-protein interactions. Curr Opin Struct Biol 39:27-38
Chen, Robert; Rishi, Harneet S; Potapov, Vladimir et al. (2015) A Barcoding Strategy Enabling Higher-Throughput Library Screening by Microscopy. ACS Synth Biol 4:1205-16
Potapov, Vladimir; Kaplan, Jenifer B; Keating, Amy E (2015) Data-driven prediction and design of bZIP coiled-coil interactions. PLoS Comput Biol 11:e1004046
Negron, Christopher; Keating, Amy E (2014) A set of computationally designed orthogonal antiparallel homodimers that expands the synthetic coiled-coil toolkit. J Am Chem Soc 136:16544-56
Kaplan, Jenifer B; Reinke, Aaron W; Keating, Amy E (2014) Increasing the affinity of selective bZIP-binding peptides through surface residue redesign. Protein Sci 23:940-53
Negron, Christopher; Keating, Amy E (2013) Multistate protein design using CLEVER and CLASSY. Methods Enzymol 523:171-90
Reinke, Aaron W; Baek, Jiyeon; Ashenberg, Orr et al. (2013) Networks of bZIP protein-protein interactions diversified over a billion years of evolution. Science 340:730-4
Ashenberg, Orr; Keating, Amy E; Laub, Michael T (2013) Helix bundle loops determine whether histidine kinases autophosphorylate in cis or in trans. J Mol Biol 425:1198-209
Yin, Wen-Bing; Reinke, Aaron W; Szilágyi, Melinda et al. (2013) bZIP transcription factors affecting secondary metabolism, sexual development and stress responses in Aspergillus nidulans. Microbiology 159:77-88
Chen, T Scott; Keating, Amy E (2012) Designing specific protein-protein interactions using computation, experimental library screening, or integrated methods. Protein Sci 21:949-63

Showing the most recent 10 out of 28 publications