The field of structural biology has developed dramatically over the last ten years, largely because of improvements in the techniques and applications of X-ray crystallography and multidimensional NMR spectroscopy. The three-dimensional structures and dynamics of macromolecules reveal mechanistic insights into protein function that cannot be gained in studies of whole cells, tissues or organisms. In turn, these insights provide molecular and cellular biologists with a rational framework for testing hypotheses about protein function. It is expected that the three-dimensional structures of proteins and their complexes will continue to have a substantial impact on our understanding of GI biology. Yet, the experimental determination of three-dimensional structures cannot keep pace with the rapid accumulation of novel gene sequences implicated in GI processes. Homology models derived from the known structures of related proteins will assist investigators in developing hypotheses that can be tested experimentally by mutagenesis and/or chemical modification of the protein and ligand. The major objective of the Protein Structure and Macromolecular Graphics (PSMG) Core is to provide DDRCC investigators with access to structural information specific to their research systems. This includes: 1) training and assistance in macromolecular modeling (homology modeling, mutational simulation, molecular docking) using continually updated graphics systems; 2) generation of structure images for slides, posters and publications; and 3) consultation and assistance with feasibility studies for protein structure determination by X-ray crystallography and/or NMR. The development of a central computing facility is a cost-effective means of utilizing the expensive software licenses and graphics workstations needed for this type of work. More importantly, it will provide investigators not principally engaged in protein structural analyses with training and guidance in molecular visualization and model building. Moreover, the PMSG facility will catalyze the structure determination process for new GI proteins by offering the resources and guidance needed for X-ray and NMR feasibility studies. The location of the facility within the Department of Biochemistry & Molecular Biophysics at the School of Medicine places it adjacent to laboratories principally focused on structural analysis of proteins and easily accessible to other users participating in the DDRCC.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK052574-02
Application #
6410332
Study Section
Special Emphasis Panel (ZDK1)
Project Start
2000-12-01
Project End
2001-11-30
Budget Start
Budget End
Support Year
2
Fiscal Year
2001
Total Cost
$180,000
Indirect Cost
Name
Washington University
Department
Type
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Gathungu, Grace; Zhang, Yuanhao; Tian, Xinyu et al. (2018) Impaired granulocyte-macrophage colony-stimulating factor bioactivity accelerates surgical recurrence in ileal Crohn's disease. World J Gastroenterol 24:623-630
Feng, Jing; Luo, Jialie; Yang, Pu et al. (2018) Piezo2 channel-Merkel cell signaling modulates the conversion of touch to itch. Science 360:530-533
Eberth, Jan M; Josey, Michele J; Mobley, Lee R et al. (2018) Who Performs Colonoscopy? Workforce Trends Over Space and Time. J Rural Health 34:138-147
Zhang, Daoxiang; Li, Lin; Jiang, Hongmei et al. (2018) Tumor-Stroma IL1?-IRAK4 Feedforward Circuitry Drives Tumor Fibrosis, Chemoresistance, and Poor Prognosis in Pancreatic Cancer. Cancer Res 78:1700-1712
Sullender, Meagan E; Baldridge, Megan T (2018) Norovirus interactions with the commensal microbiota. PLoS Pathog 14:e1007183
Brenot, Audrey; Knolhoff, Brett L; DeNardo, David G et al. (2018) SNAIL1 action in tumor cells influences macrophage polarization and metastasis in breast cancer through altered GM-CSF secretion. Oncogenesis 7:32
Luo, Jialie; Feng, Jing; Yu, Guang et al. (2018) Transient receptor potential vanilloid 4-expressing macrophages and keratinocytes contribute differentially to allergic and nonallergic chronic itch. J Allergy Clin Immunol 141:608-619.e7
Tarr, Gillian A M; Oltean, Hanna N; Phipps, Amanda I et al. (2018) Strength of the association between antibiotic use and hemolytic uremic syndrome following Escherichia coli O157:H7 infection varies with case definition. Int J Med Microbiol 308:921-926
Baumann-Dudenhoeffer, Aimee M; D'Souza, Alaric W; Tarr, Phillip I et al. (2018) Infant diet and maternal gestational weight gain predict early metabolic maturation of gut microbiomes. Nat Med 24:1822-1829
Kumar, Pardeep; Kuhlmann, F Matthew; Chakraborty, Subhra et al. (2018) Enterotoxigenic Escherichia coli-blood group A interactions intensify diarrheal severity. J Clin Invest 128:3298-3311

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