This portion of the parent application requests the resources to provide a core peptide synthesis facility for the major applications in this proposal, as well as qualified investigators throughout Oklahoma. This core facility will construct thousands of peptides ranging from four to twenty amino acids in length using standard, Fmoc chemistry. These peptides will initially be constructed on solid phase supports which can either be left in their 96-well format or cleaved to leave peptides in the fluid phase. The principal investigator of this core has over 10 years of experience using this technique and has published extensively in this area (1-11). Peptides that she has constructed have previously been used in B and T cell epitope mapping of human and monoclonal sera, inhibition of enzymatic reactivities and to map enzymatic active sites. She has previously synthesized peptides for at least two of the key investigators submitting proposals in this application. This core facility will serve as a vital resource for several of the major projects, as well as the additional signaling core. Drs. Harley and Dittmer will use peptides from the core to identify major targets of the murine and primate vaccine-induced immune response to Epstein-Barr and Kaposi Sarcoma viruses. Drs. McEver and Centola will use peptides from the core to serve as bacterial derived peptide activators of neutrophils and for immunization to develop anti-pyrin antibodies. Drs. Thompson and Teague will use peptides through the signaling core and to construct SH2 domains for use in their IL-6 signaling studies. Drs. Colleshall and the peptide signaling core will use synthetic peptides and phosphopeptides constructed in the core for pull-down experiments. Phosphopeptides have previously been constructed by this laboratory for collaborative studies with Dr. David Kem in the OUHSC Department of Endocrinology. As time and resources allow, this core peptide facility will also be available to other investigators from the Foundation, the University of Oklahoma Health Sciences Center, Tulsa University, Oklahoma State University, Oklahoma University, and Oklahoma Christian University.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR015577-02
Application #
6494180
Study Section
Special Emphasis Panel (ZRR1)
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
$256,079
Indirect Cost
Name
Oklahoma Medical Research Foundation
Department
Type
DUNS #
937727907
City
Oklahoma City
State
OK
Country
United States
Zip Code
73104
Hu, Zihua; Jiang, Kaiyu; Frank, Mark Barton et al. (2018) Modeling Transcriptional Rewiring in Neutrophils Through the Course of Treated Juvenile Idiopathic Arthritis. Sci Rep 8:7805
Hu, Zihua; Jiang, Kaiyu; Frank, Mark Barton et al. (2016) Complexity and Specificity of the Neutrophil Transcriptomes in Juvenile Idiopathic Arthritis. Sci Rep 6:27453
Molineros, Julio E; Maiti, Amit K; Sun, Celi et al. (2013) Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production. PLoS Genet 9:e1003222
Smith, Kenneth; Muther, Jennifer J; Duke, Angie L et al. (2013) Fully human monoclonal antibodies from antibody secreting cells after vaccination with Pneumovax®23 are serotype specific and facilitate opsonophagocytosis. Immunobiology 218:745-54
Dozmorov, Igor; Dominguez, Nicolas; Sestak, Andrea L et al. (2013) Evidence of dynamically dysregulated gene expression pathways in hyperresponsive B cells from African American lupus patients. PLoS One 8:e71397
Jiang, Kaiyu; Frank, Mark; Chen, Yanmin et al. (2013) Genomic characterization of remission in juvenile idiopathic arthritis. Arthritis Res Ther 15:R100
Kurien, Biji T; D'Sousa, Anil; Bruner, Benjamin F et al. (2013) Prolidase deficiency breaks tolerance to lupus-associated antigens. Int J Rheum Dis 16:674-80
Lu, Rufei; Robertson, Julie M; Bruner, Benjamin F et al. (2012) Multiple Autoantibodies Display Association with Lymphopenia, Proteinuria, and Cellular Casts in a Large, Ethnically Diverse SLE Patient Cohort. Autoimmune Dis 2012:819634
Yan, Xin; Li, Feng; Dozmorov, Igor et al. (2012) External Qi of Yan Xin Qigong induces cell death and gene expression alterations promoting apoptosis and inhibiting proliferation, migration and glucose metabolism in small-cell lung cancer cells. Mol Cell Biochem 363:245-55
Lin, C P; Adrianto, I; Lessard, C J et al. (2012) Role of MYH9 and APOL1 in African and non-African populations with lupus nephritis. Genes Immun 13:232-8

Showing the most recent 10 out of 194 publications