The primary objective of the Midwest Center for Structural Genomics (MCSG) is to operate the high-throughput protein characterization pipeline as a resource for Biology Community. The platform is well established, highly integrated and cost effective. Is comprised of the following components: bioinformatics, gene cloning, protein expression, protein purification and characterization, crystallization as well as data collection and structure determination using X-ray crystallography at 3rd generation synchrotron. As a part of its mandate, the MCSG will apply its resources for targets nominated by the individual investigators and will serve as a user facility for the U.S. academic and research institutions. The MCSG site has fully functional instrumentation and expertise in place for the task. The MCSG will actively interact with other scientists, conduct technology training and will make all results produced in the course of this program readily available to the scientific community. The MCSG is located in the Advanced Protein Characterization Facility (APCF) at Argonne National Laboratory (ANL) that is directly attached to the Advanced Photon Source (APS) at sector 19. The APCF is a state-of-the-art scientific collaborative facility that provides new, specialized laboratory space devoted to molecular, structural and systems biology.

Public Health Relevance

The high-throughput protein production and characterization technologies are well established, cost effective, and are essential to understand molecular and biochemical processes important for human health and disease, including studies of pathogens, developing new drugs, and combat antibiotic resistance. The protein production and characterization resource, located in the Advanced Protein Characterization Facility at Argonne National Laboratory, directly attached to the Advanced Photon Source, employs state-of-the-art technologies and is perfectly posed to serve the needs of U. S. academic and research institutions and provide a scientific collaboration place. Outreach to the Biology Community, hosting and training users and dissemination data and materials are essential components of this facility.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Resource-Related Research Projects (R24)
Project #
5R24GM115586-02
Application #
9115648
Study Section
Special Emphasis Panel (ZGM1)
Program Officer
Edmonds, Charles G
Project Start
2015-08-01
Project End
2018-07-31
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
2
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Chicago
Department
Biostatistics & Other Math Sci
Type
Schools of Arts and Sciences
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Gao, Jianzhao; Wu, Zhonghua; Hu, Gang et al. (2018) Survey of Predictors of Propensity for Protein Production and Crystallization with Application to Predict Resolution of Crystal Structures. Curr Protein Pept Sci 19:200-210
van den Bosch, Tijs J M; Tan, Kemin; Joachimiak, Andrzej et al. (2018) Functional profiling and crystal structures of isothiocyanate hydrolases found in gut-associated and plant pathogenic bacteria. Appl Environ Microbiol :
Michalska, Karolina; Quan Nhan, Dinh; Willett, Julia L E et al. (2018) Functional plasticity of antibacterial EndoU toxins. Mol Microbiol 109:509-527
Kryshtafovych, Andriy; Albrecht, Reinhard; Baslé, Arnaud et al. (2018) Target highlights from the first post-PSI CASP experiment (CASP12, May-August 2016). Proteins 86 Suppl 1:27-50
Khusnutdinova, Anna N; Flick, Robert; Popovic, Ana et al. (2017) Exploring Bacterial Carboxylate Reductases for the Reduction of Bifunctional Carboxylic Acids. Biotechnol J 12:
Kim, Youngchang; Chhor, Gekleng; Tsai, Ching-Sung et al. (2017) X-ray crystal structures of the pheromone-binding domains of two quorum-hindered transcription factors, YenR of Yersinia enterocolitica and CepR2 of Burkholderia cenocepacia. Proteins 85:1831-1844
Hajighasemi, Mahbod; Nocek, Boguslaw P; Tchigvintsev, Anatoli et al. (2016) Biochemical and Structural Insights into Enzymatic Depolymerization of Polylactic Acid and Other Polyesters by Microbial Carboxylesterases. Biomacromolecules 17:2027-39
Kim, Youngchang; Joachimiak, Grazyna; Bigelow, Lance et al. (2016) How Aromatic Compounds Block DNA Binding of HcaR Catabolite Regulator. J Biol Chem 291:13243-56
Jha, Ramesh K; Kern, Theresa L; Kim, Youngchang et al. (2016) A microbial sensor for organophosphate hydrolysis exploiting an engineered specificity switch in a transcription factor. Nucleic Acids Res 44:8490-500
Paul, Sangeeta; Aggarwal, Chetana; Thakur, Jyoti Kumar et al. (2015) Induction of osmoadaptive mechanisms and modulation of cellular physiology help Bacillus licheniformis strain SSA 61 adapt to salt stress. Curr Microbiol 70:610-7