This proposal requests continued support for the pre-doctoral Molecular Biophysics Training Program at Northwestern University. Since its establishment in 1990, the training program has played a major role in strengthening intellectual ties and stimulating interdisciplinary collaborations between preceptors and students in seven departments in the schools of arts & sciences, medicine, and engineering. Program preceptors conduct basic biomedical research on a broad range of topics that fall into one or more of the following categories: biophysics, biochemistry, structural biology, and computational biology. A variety of biological questions exploring molecular phenomena that impact gene transcription, translation, metal trafficking and homeostasis, electron transfer, mitochondrial positioning, viral fusion, chromosome structure, DNA-centric processes, RNA maturation, proteostasis, transport processes within the cell and across cell membranes, metabolic networks, and cellular signaling are being studied using physical approaches and/or principles. Crucial to the success of these endeavors is the ready availability of an extraordinary array of state-of-the-art instrumentation i research facilities staffed with highly-qualified personnel. Trainees of the program thus have unparalleled opportunities to receive training in many areas of contemporary molecular biophysics. Potential student trainees enter the training program through one of seven graduate programs. The training program has established a core biophysics curriculum that is taken by every trainee, allowing students from diverse backgrounds to share a common didactic experience. Trainees have numerous opportunities to develop oral presentation skills at a variety of program-sponsored forums that range from intimate settings including journal clubs and trainee seminars held every month to larger audiences at the monthly intra-mural seminars and the annual symposium. Extramural seminars and the annual symposium provide trainees opportunities for keeping abreast of the latest developments in the field and for networking with leaders in many scientific areas. Support for six trainees in their formative years of graduate education is requested, since it would allow the training program to have the greatest impact on student career development as they complete required coursework, learn to frame research questions, acquire and hone skills to answer those questions and develop skills to communicate their findings. Each trainee will be supported for a maximum of two years. Graduate training in molecular biophysics allows students to acquire a quantitative foundation based on chemical and physical principles for studying biological processes relevant to a wide range of public health issues; students trained in this area will be well-positioned to further our knowledge of human diseases and devise effective strategies for intervention.

Public Health Relevance

The overarching goal of this proposal is to train pre-doctoral graduate students of exceptional promise for scientific research careers in molecular biophysics, which is an area that embraces principles and concepts from diverse fields in the natural sciences including biology, chemistry, physics, and mathematics. A strong quantitative foundation in molecular biophysics is essential for developing an understanding of the biological processes that underlie a wide range of public health issues; this in turn can inform and ultimately lead to effective therapeutic strategies for mitigation. The training program will thus address an urgent and critical need for qualified research personnel in an area of vital importance to public health and ensure the country's continued competitiveness and leadership in this field.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
2T32GM008382-24
Application #
9073030
Study Section
Training and Workforce Development Subcommittee - D (TWD)
Program Officer
Flicker, Paula F
Project Start
1990-07-11
Project End
2021-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
24
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Purohit, Rahul; Ross, Matthew O; Batelu, Sharon et al. (2018) Cu+-specific CopB transporter: Revising P1B-type ATPase classification. Proc Natl Acad Sci U S A 115:2108-2113
Ro, Soo Y; Ross, Matthew O; Deng, Yue Wen et al. (2018) From micelles to bicelles: Effect of the membrane on particulate methane monooxygenase activity. J Biol Chem 293:10457-10465
Hong, Bong Jin; Iscen, Aysenur; Chipre, Anthony J et al. (2018) Highly Stable, Ultrasmall Polymer-Grafted Nanobins (usPGNs) with Stimuli-Responsive Capability. J Phys Chem Lett 9:1133-1139
Wytock, Thomas P; Fiebig, Aretha; Willett, Jonathan W et al. (2018) Experimental evolution of diverse Escherichia coli metabolic mutants identifies genetic loci for convergent adaptation of growth rate. PLoS Genet 14:e1007284
Tanaka, Kari J; Song, Saemee; Mason, Kevin et al. (2018) Selective substrate uptake: The role of ATP-binding cassette (ABC) importers in pathogenesis. Biochim Biophys Acta Biomembr 1860:868-877
Yeung, Priscilla S-W; Yamashita, Megumi; Ing, Christopher E et al. (2018) Mapping the functional anatomy of Orai1 transmembrane domains for CRAC channel gating. Proc Natl Acad Sci U S A 115:E5193-E5202
Chan, Clarence W; Kiesel, Benjamin R; Mondragón, Alfonso (2018) Crystal Structure of Human Rpp20/Rpp25 Reveals Quaternary Level Adaptation of the Alba Scaffold as Structural Basis for Single-stranded RNA Binding. J Mol Biol 430:1403-1416
Chen, WeiTing; Ping, Holly A; Lackner, Laura L (2018) Direct membrane binding and self-interaction contribute to Mmr1 function in mitochondrial inheritance. Mol Biol Cell 29:2346-2357
Daffern, Nicolas; Chen, Zhonglei; Zhang, Yongbo et al. (2018) Solution Nuclear Magnetic Resonance Studies of the Ligand-Binding Domain of an Orphan Nuclear Receptor Reveal a Dynamic Helix in the Ligand-Binding Pocket. Biochemistry 57:1977-1986
Yeung, Priscilla See-Wai; Prakriya, Murali (2018) The exquisitely cooperative nature of Orai1 channel activation. J Gen Physiol 150:1352-1355

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