(Macromolecular Crystallography Laboratory) The three-dimensional structure determination of macromolecules such as proteins and nucleic acids using X- ray crystallography provides unique insights into the function of the molecule or molecular complex. The OU- Norman Macromolecular Crystallography Laboratory Core (MCL) provides expertise and state-of-the-art instrumentation to support the Oklahoma COBRE in Structure Biology (OCSB) affiliated research groups and other research groups involved in structural biology research, particularly in protein crystallography, across the State of Oklahoma. The MCL accomplishes this by utilizing robotic instrumentation for the screening of crystallization conditions, the utilization of a high flux micro focus X-ray generator and a state-of-the-art hybrid pixel X-ray detector for data collection along with up to date maintenance of computational resources to process and determine the structure of the macromolecules of interest. The MCL director, Dr. Leonard Thomas, is a full time Ph.D. crystallographer. The facility also employs a Graduate Assistant to aid in the screening of crystallization conditions and the preparation of samples for collection of X-ray data. The MCL provides training to students, postdoctoral fellows and faculty who are interested in macromolecular structure determination. During the OCSB Phase I funding the MCL user base has been greatly expanded and the facility will continue to expand its user base by providing expertise, state-of-the-art facilities and training during the OCSB Phase II.

Public Health Relevance

The OU-Norman Macromolecular Crystallography Laboratory Core provides expertise and instrumentation to determine the three-dimensional structures of proteins for investigators involved in the study of disease mechanisms and drug design. The facility also provides training in all aspects of protein crystallography.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM103640-09
Application #
9934238
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
9
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Oklahoma Norman
Department
Type
DUNS #
848348348
City
Norman
State
OK
Country
United States
Zip Code
73019
Hebdon, Skyler D; Menon, Smita K; Richter-Addo, George B et al. (2018) Regulatory Targets of the Response Regulator RR_1586 from Clostridioides difficile Identified Using a Bacterial One-Hybrid Screen. J Bacteriol 200:
Cruz-Reyes, Jorge; Mooers, Blaine H M; Doharey, Pawan K et al. (2018) Dynamic RNA holo-editosomes with subcomplex variants: Insights into the control of trypanosome editing. Wiley Interdiscip Rev RNA 9:e1502
Booe, Jason M; Warner, Margaret L; Roehrkasse, Amanda M et al. (2018) Probing the Mechanism of Receptor Activity-Modifying Protein Modulation of GPCR Ligand Selectivity through Rational Design of Potent Adrenomedullin and Calcitonin Gene-Related Peptide Antagonists. Mol Pharmacol 93:355-367
Muthuramalingam, Meenakumari; White, John C; Murphy, Tamiko et al. (2018) The toxin from a ParDE toxin-antitoxin system found in Pseudomonas aeruginosa offers protection to cells challenged with anti-gyrase antibiotics. Mol Microbiol :
Roehrkasse, Amanda M; Booe, Jason M; Lee, Sang-Min et al. (2018) Structure-function analyses reveal a triple ?-turn receptor-bound conformation of adrenomedullin 2/intermedin and enable peptide antagonist design. J Biol Chem 293:15840-15854
Van Orden, Mason J; Klein, Peter; Babu, Kesavan et al. (2017) Conserved DNA motifs in the type II-A CRISPR leader region. PeerJ 5:e3161
Murugan, Karthik; Babu, Kesavan; Sundaresan, Ramya et al. (2017) The Revolution Continues: Newly Discovered Systems Expand the CRISPR-Cas Toolkit. Mol Cell 68:15-25
Li, Yangxiong; Lavey, Nathan P; Coker, Jesse A et al. (2017) Consequences of Depsipeptide Substitution on the ClpP Activation Activity of Antibacterial Acyldepsipeptides. ACS Med Chem Lett 8:1171-1176
Wang, Bing; Powell, Samantha M; Guan, Ye et al. (2017) Nitrosoamphetamine binding to myoglobin and hemoglobin: Crystal structure of the H64A myoglobin-nitrosoamphetamine adduct. Nitric Oxide 67:26-29
Sundaresan, Ramya; Parameshwaran, Hari Priya; Yogesha, S D et al. (2017) RNA-Independent DNA Cleavage Activities of Cas9 and Cas12a. Cell Rep 21:3728-3739

Showing the most recent 10 out of 47 publications