The Chemistry Biology Interface Training Program (CBIT) provides graduate students at the University of Wisconsin-Madison with a training experience designed to allow them to apply interdisciplinary approaches and ideas to make major breakthroughs. This project has two inter-related objectives. The first is to train graduate students to address synthetic and mechanistic problems that transcend the traditional boundaries of chemistry and biology. In this way, trainees will be prepared for careers in which they illuminate key issues in human health through innovative approaches. The second is to provide career advice and assistance so that trainees can use their training and skills to maximize their impact. These objectives are achieved through the unique training plan offered graduate student trainees. This renewal requests support for twelve predoctoral trainees per year; each trainee will be appointed to the program for up to three years. CBIT trainees enroll in three courses including a didactic course in the field of chemical biology that introduces graduate students to research and concepts at the intersection of chemistry and biology, an advanced literature seminar course in chemical biology where students present and discuss recent key publications in the field, and a research seminar in which trainees present their personal research results. Through this program, CBIT trainees receive experience in analysis of the literature, grant writing, and peer review. They also develop their oral communication skills through giving different types of presentations and receiving extensive feedback on how to enhance the effectiveness of their presentations. Another key element of the CBIT is career advising and development for all trainees, which occurs through the creation of individual development plans and participation in a newly implemented Midwest Chemistry Biology Interface Career Development Conference. Finally, CBIT trainees benefit from the opportunity to participate in a 10-12-week internship. The goal of this feature is to immerse them in an environment that provides direct experience in a relevant setting distinct from a research university.

Public Health Relevance

The Chemistry Biology Interface Training Program (CBIT) provides graduate students at the University of Wisconsin-Madison with a training experience designed to allow them to use interdisciplinary ideas and approaches to make major biomedical breakthroughs. The program trains graduate students to address problems that transcend the traditional boundaries of chemistry and biology and also provides trainees with career plan development assistance. Training at the chemistry---biology interface is ideal preparation for designing, discovering, and developing the next generation of therapeutic agents, which will directly impact human health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM008505-24
Application #
9302785
Study Section
NIGMS Initial Review Group (TWD)
Program Officer
Fabian, Miles
Project Start
1993-09-01
Project End
2019-06-30
Budget Start
2017-07-01
Budget End
2018-06-30
Support Year
24
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Lee, Hye Jin; Ehlerding, Emily B; Cai, Weibo (2018) Antibody-Based Tracers for PET/SPECT Imaging of Chronic Inflammatory Diseases. Chembiochem :
Wei, Weijun; Ni, Dalong; Ehlerding, Emily B et al. (2018) PET Imaging of Receptor Tyrosine Kinases in Cancer. Mol Cancer Ther 17:1625-1636
Ni, Dalong; Ehlerding, Emily B; Cai, Weibo (2018) Multimodality Imaging Agents with PET as the Fundamental Pillar. Angew Chem Int Ed Engl :
Ellison, Aubrey J; Raines, Ronald T (2018) A pendant peptide endows a sunscreen with water-resistance. Org Biomol Chem 16:7139-7142
Palmer, Andrew G; Senechal, Amanda C; Haire, Timothy C et al. (2018) Selection of Appropriate Autoinducer Analogues for the Modulation of Quorum Sensing at the Host-Bacterium Interface. ACS Chem Biol 13:3115-3122
Ni, Dalong; Jiang, Dawei; Ehlerding, Emily B et al. (2018) Radiolabeling Silica-Based Nanoparticles via Coordination Chemistry: Basic Principles, Strategies, and Applications. Acc Chem Res 51:778-788
England, Christopher G; Jiang, Dawei; Ehlerding, Emily B et al. (2018) 89Zr-labeled nivolumab for imaging of T-cell infiltration in a humanized murine model of lung cancer. Eur J Nucl Med Mol Imaging 45:110-120
Ehlerding, Emily B; Sun, Lingyi; Lan, Xiaoli et al. (2018) Dual-Targeted Molecular Imaging of Cancer. J Nucl Med 59:390-395
Liu, Zhen; Ehlerding, Emily B; Cai, Weibo et al. (2018) One-step synthesis of an 18F-labeled boron-derived methionine analog: a substitute for 11C-methionine? Eur J Nucl Med Mol Imaging 45:582-584
Hodges, Heather L; Brown, Robert A; Crooks, John A et al. (2018) Imaging mycobacterial growth and division with a fluorogenic probe. Proc Natl Acad Sci U S A 115:5271-5276

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