This is the second renewal of Chemistry-Biology Interface (CBI) training grant T32 GM08804. We have designed an interdisciplinary program for training students (and faculty) at the interface of biological, medicinal, and traditional chemistr, called the Biological Chemistry Program (BCP). The BCP began in the fall of 2000 and provides a focused, cross-disciplinary education for students at the interface of biology and chemistry. The BCP is fully integrated into the departments of Chemistry and Biochemistry (Colleges of Science and Medicine), and Pharmacology and Toxicology (Division of Drug Discovery and Development, College of Pharmacy). Students may obtain a degree in Chemistry, Biochemistry, or Pharmaceutical Sciences while following the Biological Chemistry Training Program. Students undertake graduate coursework in Chemistry and Biology, perform research rotations in at least two research disciplines and participate in the weekly BCP Research Forum, where students and faculty present research results. Importantly, students may work with anyone in the program, regardless of departmental affiliation, allowing for true multidisciplinary research efforts. The training faculty includes 30 highly active research groups. Students remain in the BCP until graduation. There are 39 students currently following the training program, 23 of whom are training grant eligible. An additional 15 students (14 TGE) are expected to join the BCP next fall, out of an entering class of 35 students. Training grant slots are generally awarded for years 2 and 3 in the program, allowing training grant recipients great flexibility in assemblin a multidisciplinary research project. Fellowships are awarded in May to help first-year students assemble a broad- based mentoring team. For years 11-15, we request 6 training grant slots per year, allowing for ~20% of our training-grant-eligible students to be funded at any given time. Training at the Chemistry-Biology Interface is highly relevant for advances in public health. By blending Chemistry, Medicinal Chemistry and Biochemistry, our trainees are poised to make the next breakthroughs in drug discovery, disease detection, disease prevention, and the discovery of the underlying principles governing life and disease. Our 42 BCP graduates populate both academic science centers and disease-oriented private-sector companies.

Public Health Relevance

The Biological Chemistry Program trains PhD students at the interface of Chemistry and Biology, with particular emphases on drug discovery and the underlying principles governing healthy cells. Our students are poised to make the next great discoveries in disease detection and cures.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008804-15
Application #
9509461
Study Section
NIGMS Initial Review Group (TWD)
Program Officer
Fabian, Miles
Project Start
2003-07-01
Project End
2019-06-30
Budget Start
2018-07-01
Budget End
2019-06-30
Support Year
15
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Arizona
Department
Biochemistry
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Dodson, Matthew; Liu, Pengfei; Jiang, Tao et al. (2018) Increased O-GlcNAcylation of SNAP29 drives arsenic-induced autophagic dysfunction. Mol Cell Biol :
Zhang, Jiantao; Hu, Yanmei; Foley, Christopher et al. (2018) Exploring Ugi-Azide Four-Component Reaction Products for Broad-Spectrum Influenza Antivirals with a High Genetic Barrier to Drug Resistance. Sci Rep 8:4653
Musharrafieh, Rami; Ma, Chunlong; Wang, Jun (2018) Profiling the in vitro drug-resistance mechanism of influenza A viruses towards the AM2-S31N proton channel blockers. Antiviral Res 153:10-22
Foley, Christopher; Shaw, Arthur; Hulme, Christopher (2018) Aza-Riley Oxidation of Ugi-Azide and Ugi-3CR Products toward Vicinal Tricarbonyl Amides: Two-Step MCR-Oxidation Methodology Accessing Functionalized ?,?-Diketoamides and ?,?-Diketotetrazoles. Org Lett 20:1275-1278
Wales, Jessica A; Chen, Cheng-Yu; Breci, Linda et al. (2018) Discovery of stimulator binding to a conserved pocket in the heme domain of soluble guanylyl cyclase. J Biol Chem 293:1850-1864
Tillotson, Joseph; Zerio, Christopher J; Harder, Bryan et al. (2017) Arsenic Compromises Both p97 and Proteasome Functions. Chem Res Toxicol 30:1508-1514
Parent, Kate L; Hill, Daniel F; Crown, Lindsey M et al. (2017) Platform to Enable Combined Measurement of Dopamine and Neural Activity. Anal Chem 89:2790-2799
Ambrose, Andrew J; Santos, Evelyne A; Jimenez, Paula C et al. (2017) Ritterostatin GN 1N , a Cephalostatin-Ritterazine Bis-steroidal Pyrazine Hybrid, Selectively Targets GRP78. Chembiochem 18:506-510
Montfort, William R; Wales, Jessica A; Weichsel, Andrzej (2017) Structure and Activation of Soluble Guanylyl Cyclase, the Nitric Oxide Sensor. Antioxid Redox Signal 26:107-121
Hu, Yanmei; Zhang, Jiantao; Musharrafieh, Rami Ghassan et al. (2017) Discovery of dapivirine, a nonnucleoside HIV-1 reverse transcriptase inhibitor, as a broad-spectrum antiviral against both influenza A and B viruses. Antiviral Res 145:103-113

Showing the most recent 10 out of 72 publications