Five years of support are requested to establish a program for development of junior faculty with research interests in Protein Structure and Function, with the goal of enabling them to become fully competitive for NIH grant support. Four Ph.D.-granting institutions in Kansas are participating, including KU-Lawrence, K-State University, KU-School of Medicine, and Wichita State University. The Principal Investigator, co-investigator, and a strong group of established, NIH-funded faculty, along with outstanding scientists on an External Advisory Committee (EAC), will provide mentoring and assistance to new faculty, not only in establishing highly competitive research programs in the study of protein structure and function but in their overall development as academic scientists. Individual mentoring plans with specific milestones form the basis for the development program. This will be supplemented with a seminar series by prominent scientists alternating with research presentations by COBRE investigators and workshops dealing with technical aspects of protein analysis, publishing, grant writing, and lab management. One administrative and two scientific Cores will be established to administer the program and provide high caliber technical expertise and instrumentation. Protein Structure and Function was selected as a theme because (1) detailed understanding of proteins is the next great challenge in overcoming diseases, (2) a strong cadre of senior faculty in Kansas are working in this area, and (3) current and future hiring plans for new faculty throughout the State of Kansas emphasize studies in protein structure and function. This focus on multi-disciplinary research on proteins enables us to capitalize on recent University investments in research infrastructure, and to obtain substantial institutional support for the proposed program in the form of FTEs, new research instrumentation, and space. Six faculty have been selected for 2-3 years of support, based on scientific merit, relevance for the COBRE theme, potential to benefit from the mentoring program and the Core labs, and likelihood of developing their project to compete successfully for NIH grants in the future. Progress toward the goals of the Program will be monitored by self-study and by Internal and External Advisory Committees; the latter will also review proposals and applications from new junior faculty for COBRE support.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR017708-03
Application #
6798763
Study Section
Special Emphasis Panel (ZRR1-RI-A (03))
Program Officer
Canto, Maria Teresa
Project Start
2002-09-30
Project End
2007-06-30
Budget Start
2004-07-01
Budget End
2005-06-30
Support Year
3
Fiscal Year
2004
Total Cost
$2,159,004
Indirect Cost
Name
University of Kansas Lawrence
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
076248616
City
Lawrence
State
KS
Country
United States
Zip Code
66045
Garabedian, Alyssa; Baird, Matthew A; Porter, Jacob et al. (2018) Linear and Differential Ion Mobility Separations of Middle-Down Proteoforms. Anal Chem 90:2918-2925
Jeanne Dit Fouque, Kevin; Garabedian, Alyssa; Porter, Jacob et al. (2017) Fast and Effective Ion Mobility-Mass Spectrometry Separation of d-Amino-Acid-Containing Peptides. Anal Chem 89:11787-11794
Alaofi, Ahmed; Farokhi, Elinaz; Prasasty, Vivitri D et al. (2017) Probing the interaction between cHAVc3 peptide and the EC1 domain of E-cadherin using NMR and molecular dynamics simulations. J Biomol Struct Dyn 35:92-104
Pang, Xiao-Yan; Wang, Suya; Jurczak, Michael J et al. (2017) Retinol saturase modulates lipid metabolism and the production of reactive oxygen species. Arch Biochem Biophys 633:93-102
McNiff, Michaela L; Chadwick, Jennifer S (2017) Metal-bound claMP Tag inhibits proteolytic cleavage. Protein Eng Des Sel 30:467-475
McNiff, M L; Haynes, E P; Dixit, N et al. (2016) Thioredoxin fusion construct enables high-yield production of soluble, active matrix metalloproteinase-8 (MMP-8) in Escherichia coli. Protein Expr Purif 122:64-71
Johnson, Troy A; Mcleod, Matthew J; Holyoak, Todd (2016) Utilization of Substrate Intrinsic Binding Energy for Conformational Change and Catalytic Function in Phosphoenolpyruvate Carboxykinase. Biochemistry 55:575-87
Tucker, Jenifer K; McNiff, Michaela L; Ulapane, Sasanka B et al. (2016) Mechanistic investigations of matrix metalloproteinase-8 inhibition by metal abstraction peptide. Biointerphases 11:021006
Yadav, Rahul; Vattepu, Ravi; Beck, Moriah R (2016) Phosphoinositide Binding Inhibits Actin Crosslinking and Polymerization by Palladin. J Mol Biol 428:4031-4047
Gurung, Ritu; Yadav, Rahul; Brungardt, Joseph G et al. (2016) Actin polymerization is stimulated by actin cross-linking protein palladin. Biochem J 473:383-96

Showing the most recent 10 out of 256 publications