In this competing renewal application of a Merit award, Dr. DiMaio describes a series of experiments to investigate various aspects of the interaction between the bovine papillomavirus type 1 (BPV-1) E5 protein and the cellular PDGF beta receptor. Based upon studies performed during the prior funding period, Dr. DiMaio has proposed a model to explain how the E5 protein forms a dimer and binds to the PDGF beta receptor, and how this interaction results in receptor activation that contributes to cellular transformation.
Six aims are proposed: 1) to determine the molecular basis for the ability of E5 to discriminate between the PDGF beta receptor and = the closely related PDGF alpha receptor. 2) To identify the helical interface that mediates E5 dimerization, 3) to test the model that each E5 monomer contributes to the productive binding of E5 dimer to PDGF beta, 4) to characterize the signaling that occurs as a consequence of E5's activation of the PDGF beta receptor, 5) to test the hypothesis that certain mutants of E5 can interfere with PDGF beta signaling and 6) to identify novel peptide sequences that can contribute to the multimerization and activation of PDGF beta receptor

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA037157-17
Application #
6196531
Study Section
Virology Study Section (VR)
Program Officer
Read-Connole, Elizabeth Lee
Project Start
1984-04-01
Project End
2005-06-30
Budget Start
2000-07-01
Budget End
2001-06-30
Support Year
17
Fiscal Year
2000
Total Cost
$447,589
Indirect Cost
Name
Yale University
Department
Genetics
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Petti, Lisa M; Marlatt, Sara A; Luo, Yong et al. (2018) Regulation of C-C chemokine receptor 5 (CCR5) stability by Lys197 and by transmembrane protein aptamers that target it for lysosomal degradation. J Biol Chem 293:8787-8801
He, Li; Steinocher, Helena; Shelar, Ashish et al. (2017) Single methyl groups can act as toggle switches to specify transmembrane Protein-protein interactions. Elife 6:
Karabadzhak, Alexander G; Petti, Lisa M; Barrera, Francisco N et al. (2017) Two transmembrane dimers of the bovine papillomavirus E5 oncoprotein clamp the PDGF ? receptor in an active dimeric conformation. Proc Natl Acad Sci U S A 114:E7262-E7271
DiMaio, Daniel (2016) Thank You, Edward. Merci, Louis. PLoS Pathog 12:e1005320
Heim, Erin N; Marston, Jez L; Federman, Ross S et al. (2015) Biologically active LIL proteins built with minimal chemical diversity. Proc Natl Acad Sci U S A 112:E4717-25
Dimaio, Daniel (2014) Is virology dead? MBio 5:e01003-14
DiMaio, Daniel (2014) Viral miniproteins. Annu Rev Microbiol 68:21-43
Chacón, Kelly M; Petti, Lisa M; Scheideman, Elizabeth H et al. (2014) De novo selection of oncogenes. Proc Natl Acad Sci U S A 111:E6-E14
Cohen, Emily B; Jun, Susan J; Bears, Zachary et al. (2014) Mapping the homodimer interface of an optimized, artificial, transmembrane protein activator of the human erythropoietin receptor. PLoS One 9:e95593
DiMaio, Daniel; Petti, Lisa M (2013) The E5 proteins. Virology 445:99-114

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