This re-submission proposal is a request for a renewal of an existing program at the University of Pennsylvania in Structural Biology and Molecular Biophysics. This pre-doctoral Training Program is a University-wide, interdepartmental and inter-school program that was designed to provide teaching and research experience in the application of physical methods towards biological problems. This past few years the program has been extensively modified both in philosophy and organization. The training program brings together 23 faculty trainers dedicated to providing the highest standards for graduate education. In this resubmission we have made many changes that strengthen all aspects of this program. In particular, we have recruited new faculty, obtained instrumentation, developed a new curriculum and revamped the organization and administrative aspects of the program. We have maintained our strength in spectroscopic analysis of proteins while adding 5 new faculty in structural biology. The training program molds a highly interactive group of students and faculty from many departments into a well organized unit who are dedicated to the mission of this program and the application of physical methodologies to solve significant biological and medically relevant problems. The goal of this training program is to exploit the resources available at the University of Pennsylvania to generate an integrated structural biology and molecular biophysics training program. Specifically the program is intended to provide students with a well rounded didactic training in the biological and physical sciences. The training program will produce the next generation of scientists, that are competent in both identifying the important biological problems of the 21st century and the ability to tackle these problems using the appropriate tools of molecular biophysics.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
2T32GM008275-11A1
Application #
2720966
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Project Start
1988-09-30
Project End
2004-06-30
Budget Start
1999-07-01
Budget End
2000-06-30
Support Year
11
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Biochemistry
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Sutherland, George A; Grayson, Katie J; Adams, Nathan B P et al. (2018) Probing the quality control mechanism of the Escherichia coli twin-arginine translocase with folding variants of a de novo-designed heme protein. J Biol Chem 293:6672-6681
O'Brien, Evan S; Lin, Danny W; Fuglestad, Brian et al. (2018) Improving yields of deuterated, methyl labeled protein by growing in H2O. J Biomol NMR 71:263-273
Vara, Brandon A; Li, Xingpin; Berritt, Simon et al. (2018) Scalable thioarylation of unprotected peptides and biomolecules under Ni/photoredox catalysis. Chem Sci 9:336-344
Caro, José A; Wand, A Joshua (2018) Practical aspects of high-pressure NMR spectroscopy and its applications in protein biophysics and structural biology. Methods 148:67-80
Bagchi, Atrish; Haidar, Jaafar N; Eastman, Scott W et al. (2018) Molecular Basis for Necitumumab Inhibition of EGFR Variants Associated with Acquired Cetuximab Resistance. Mol Cancer Ther 17:521-531
Yuan, Zuo-Fei; Sidoli, Simone; Marchione, Dylan M et al. (2018) EpiProfile 2.0: A Computational Platform for Processing Epi-Proteomics Mass Spectrometry Data. J Proteome Res 17:2533-2541
Guo, Lin; Kim, Hong Joo; Wang, Hejia et al. (2018) Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains. Cell 173:677-692.e20
Walters, Christopher R; Ferrie, John J; Petersson, E James (2018) Dithioamide substitutions in proteins: effects on thermostability, peptide binding, and fluorescence quenching in calmodulin. Chem Commun (Camb) 54:1766-1769
Armour, Sean M; Remsberg, Jarrett R; Damle, Manashree et al. (2017) An HDAC3-PROX1 corepressor module acts on HNF4? to control hepatic triglycerides. Nat Commun 8:549
Das, Arunika; Smoak, Evan M; Linares-Saldana, Ricardo et al. (2017) Centromere inheritance through the germline. Chromosoma 126:595-604

Showing the most recent 10 out of 209 publications