We propose to establish a Biomedical Technology Research Center (BTRC) in High Performance Computing for Multiscale Modeling of Biological Systems, as a joint effort between the U of Pittsburgh (Pitt; lead institution), Carnegie Mellon U (CMU), the Pittsburgh Supercomputing Center (PSC) and Salk Institute. The Center will develop technology and tools to facilitate research and training at the interface between computing technology and life sciences, and focus on a deeper understanding ofthe molecular and cellular organization and mechanisms that underlie synaptic signaling and regulation, thus facilitating the discovery of new treatments against nervous system disorders. The goal is to start filling the gap between modeling efforts at disparate scales of structural biology, cellular microphysiology and large scale image analysis. Computational technology research and development (TR&D) studies will be conducted in (i) molecular modeling and simulations, (ii) cell modeling and simulations, and (iii) bioimage processing and analysis. These activities will emphasize developing tools to tackle the spatial and molecular complexity inherent in signal transmission and will be driven by five experimental driving biomedical projects (at Pitt, Caltech, Harvard and UT Southwestern Medical Center) on (i) neurotransmitter transport by excitatory amino acid transporters, (ii) activation of CaMKII in spines, (iii) dopamine transporter trafficking in dopamie neurons, (iv) Itk as a regulator of T cell signaling, and (iv) neuronal circuit reconstruction from serial section transmission electron microscopy images. The Center will carry out a vigorous training and dissemination program in its areas of concentration, it will leverage the capabilities of the PSC which has been home to a BTRC for more than twenty years and, besides its biomedical technology research, has a long track record of service, training and dissemination. It will also take advantage ofthe unique strengths ofthe Computational & Systems Biology Department at Pitt, and the Lane Center for Computational Biology at CMU, building on numerous successful collaborative research and training efforts between the two universities, and cutting-edge research at the Computational Neurobiology Laboratory at the Salk Institute.

Public Health Relevance

This project will develop powerful computational tools for analyzing and relating observations of neural systems and the brain at scales varying from molecular to cellular to tissue. These, will provide insights into mechanisms that distinguish normal from defective proteins, cells or organisms. These results will help accelerate the discovery of new pharmacological approaches for treating nervous system diseases associated with signaling disorders

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Biotechnology Resource Grants (P41)
Project #
4P41GM103712-05
Application #
9118310
Study Section
Special Emphasis Panel (ZRG1-BST-N (40)P)
Program Officer
Ravichandran, Veerasamy
Project Start
2012-09-24
Project End
2017-07-31
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
5
Fiscal Year
2016
Total Cost
$1,557,310
Indirect Cost
$167,769
Name
University of Pittsburgh
Department
Biology
Type
Schools of Medicine
DUNS #
004514360
City
Pittsburgh
State
PA
Country
United States
Zip Code
15213
Bromer, Cailey; Bartol, Thomas M; Bowden, Jared B et al. (2018) Long-term potentiation expands information content of hippocampal dentate gyrus synapses. Proc Natl Acad Sci U S A 115:E2410-E2418
Spealman, Pieter; Naik, Armaghan W; May, Gemma E et al. (2018) Conserved non-AUG uORFs revealed by a novel regression analysis of ribosome profiling data. Genome Res 28:214-222
Debiec, Karl T; Whitley, Matthew J; Koharudin, Leonardus M I et al. (2018) Integrating NMR, SAXS, and Atomistic Simulations: Structure and Dynamics of a Two-Domain Protein. Biophys J 114:839-855
Pino-Angeles, Almudena; Lazaridis, Themis (2018) Effects of Peptide Charge, Orientation, and Concentration on Melittin Transmembrane Pores. Biophys J 114:2865-2874
Ponzoni, Luca; Bahar, Ivet (2018) Structural dynamics is a determinant of the functional significance of missense variants. Proc Natl Acad Sci U S A 115:4164-4169
Jia, Shanhang; Miedel, Mark T; Ngo, Marilyn et al. (2018) Clinically Observed Estrogen Receptor Alpha Mutations within the Ligand-Binding Domain Confer Distinguishable Phenotypes. Oncology 94:176-189
Sauerwald, Natalie; Kingsford, Carl (2018) Quantifying the similarity of topological domains across normal and cancer human cell types. Bioinformatics 34:i475-i483
Cheng, Mary Hongying; Kaya, Cihan; Bahar, Ivet (2018) Quantitative Assessment of the Energetics of Dopamine Translocation by Human Dopamine Transporter. J Phys Chem B 122:5336-5346
Lee, Ji Young; Krieger, James; Herguedas, Beatriz et al. (2018) Druggability Simulations and X-Ray Crystallography Reveal a Ligand-Binding Site in the GluA3 AMPA Receptor N-Terminal Domain. Structure :
Han, Ligong; Murphy, Robert F; Ramanan, Deva (2018) Learning Generative Models of Tissue Organization with Supervised GANs. IEEE Winter Conf Appl Comput Vis 2018:682-690

Showing the most recent 10 out of 180 publications