The X-ray Crystallography Shared Facility provides a unique, state-of-the art crystallography facility for Cancer Center members and other regional scientists. In the last five years, the facility has acquired extensive high through put capabilities, including dedicated access to two beamlines at the Argonne Synchrotron Facility, a fully-automated nano-crystallization laboratory and a liquid diffusion crystallization via an automated microfluidics system. The facility also has four rotating anode generators with multiple image plate detection systems, crystallographic computing and graphics packages to support structural studies. The facility is currently supporting more than twenty different cancer related projects. The Core is currently being used to support structural studies of major Cancer Center programs such as structural studies, of lymphokines and cytokines, the Cancer Center SPORE program involving 'preclinical/clinical development of novel retinoids for breast cancer prevention'. The Core is currently being used to crystallize novel retinoid-retinoic acid nuclear receptor complexes (RARs) to support drug development to prevent skin cancer and to treat breast cancer and leukemia. Other structural studies include ligand/DNA interactions, chaperone proteins, Apo-lipoprotein A-I, a DNA repair endonuclease, several different toll-like receptors, Mark-3 kinase and the development of novel pirn kinase inhibitors. The value of the Core's novel crystallization capabilities is highlighted by results produced from multiple investigators from the NCI. In the last six months the Core was able to produce crystals of five different NCI proteins.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013148-34
Application #
7102511
Study Section
Subcommittee G - Education (NCI)
Project Start
2005-04-28
Project End
2010-03-31
Budget Start
2005-04-28
Budget End
2006-03-31
Support Year
34
Fiscal Year
2005
Total Cost
$175,589
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Gowda, Pramod S; Wildman, Benjamin J; Trotter, Timothy N et al. (2018) Runx2 Suppression by miR-342 and miR-363 Inhibits Multiple Myeloma Progression. Mol Cancer Res 16:1138-1148
Dix, Daniel B; McDonald, Andrew M; Gordetsky, Jennifer B et al. (2018) How Would MRI-targeted Prostate Biopsy Alter Radiation Therapy Approaches in Treating Prostate Cancer? Urology 122:139-146
Prince, Andrew C; Moore, Lindsay S; Tipirneni, Kiranya E et al. (2018) Evaluation of optical imaging agents in a fluorescence-guided surgical model of head and neck cancer. Surg Oncol 27:225-230
Gangrade, Abhishek; Pathak, Vibha; Augelli-Szafran, Corinne E et al. (2018) Preferential Inhibition of Wnt/?-Catenin Signaling by Novel Benzimidazole Compounds in Triple-Negative Breast Cancer. Int J Mol Sci 19:
Buford, Thomas W; Carter, Christy S; VanDerPol, William J et al. (2018) Composition and richness of the serum microbiome differ by age and link to systemic inflammation. Geroscience 40:257-268
Kim, Harrison (2018) Variability in Quantitative DCE-MRI: Sources and Solutions. J Nat Sci 4:
Pruitt, Hawley C; Metge, Brandon J; Weeks, Shannon E et al. (2018) Conditional knockout of N-Myc and STAT interactor disrupts normal mammary development and enhances metastatic ability of mammary tumors. Oncogene 37:1610-1623
Frugé, Andrew D; Van der Pol, William; Rogers, Laura Q et al. (2018) Fecal Akkermansia muciniphila Is Associated with Body Composition and Microbiota Diversity in Overweight and Obese Women with Breast Cancer Participating in a Presurgical Weight Loss Trial. J Acad Nutr Diet :
Jo, SeongHo; Chen, Junqin; Xu, Guanlan et al. (2018) miR-204 Controls Glucagon-Like Peptide 1 Receptor Expression and Agonist Function. Diabetes 67:256-264
Boitano, Teresa K L; Smith, Haller J; Rushton, Tullia et al. (2018) Impact of enhanced recovery after surgery (ERAS) protocol on gastrointestinal function in gynecologic oncology patients undergoing laparotomy. Gynecol Oncol 151:282-286

Showing the most recent 10 out of 747 publications