The signaling pathways leading to the activation of the Rel/NFkappaB family of transcription factors are subjected to a novel level of regulation in which the ubiquitously expressed Rel/NFkappaB proteins are sequestered in the cytoplasm by inhibitor IkappaB proteins. The focus of the following research is to understand the molecular detains underlying the inhibitory mechanism employed by IkappaB proteins. The proposed research will provide a molecular for the behavior of the NFkappaB/IkappaB signaling pathway. We are using two different approaches for our investigations. High resolution X-ray crystallography will be integrated with biochemical and mutational analysis. Our research will address two central questions: First, how do IkappaB proteins selectively inhibit a unique subset of Rel/NFkappaB dimers. The proposed work relies on our ability to produce large amounts of highly pure proteins. This work has led us to obtain well-ordered crystals for structure analysis. Upon completion of the proposed experiments, the chemical rules that determine specificity and affinity of different NFkappaB/IkappaB complexes will be elucidated. These experiments will allow us to propose a model for how different complex formation between Rel/NFkappaB and IkappaB ultimately dictates the fate of a specific cell type.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA078749-02
Application #
6174375
Study Section
Biophysical Chemistry Study Section (BBCB)
Program Officer
Gallahan, Daniel L
Project Start
1999-04-01
Project End
2002-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
2
Fiscal Year
2000
Total Cost
$206,176
Indirect Cost
Name
University of California San Diego
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Malek, Shiva; Huang, De-Bin; Huxford, Tom et al. (2003) X-ray crystal structure of an IkappaBbeta x NF-kappaB p65 homodimer complex. J Biol Chem 278:23094-100
Chen, Yi; Wu, Joann; Ghosh, Gourisankar (2003) KappaB-Ras binds to the unique insert within the ankyrin repeat domain of IkappaBbeta and regulates cytoplasmic retention of IkappaBbeta x NF-kappaB complexes. J Biol Chem 278:23101-6
Malek, S; Chen, Y; Huxford, T et al. (2001) IkappaBbeta, but not IkappaBalpha, functions as a classical cytoplasmic inhibitor of NF-kappaB dimers by masking both NF-kappaB nuclear localization sequences in resting cells. J Biol Chem 276:45225-35
Phelps, C B; Sengchanthalangsy, L L; Huxford, T et al. (2000) Mechanism of I kappa B alpha binding to NF-kappa B dimers. J Biol Chem 275:29840-6
Huxford, T; Malek, S; Ghosh, G (2000) Preparation and crystallization of dynamic NF-kappa B.Ikappa B complexes. J Biol Chem 275:32800-6