The development of innovative measurement and analysis tools enables new information on brain function, often allowing a range of novel questions to be addressed. Rapidly evolving metabolomics, peptidomics and proteomics tools facilitate new findings in both discovery and targeted modes. The Neuroproteomics and Neurometabolomics Center on Cell-Cell Signaling provides high-end 'omics-scale characterization of the small molecules, peptides and proteins for samples obtained from brain sub-regions like defined nuclei and even specific single cells. Our sampling methods allow molecular localization via discrete cell isolation, mass spectrometry imaging, measurement of activity dependent release, and quantitation of level changes as a function of exposure to drugs. We then characterize the most important molecular targets in these samples using metabolomics, peptidomics and proteomics via a broad array of mass spectrometry-based technologies. Finally, we provide the critical expertise for capturing the value of data via expert bioinformatics support that integrates disparate data types, develops advanced analytical approaches for complex metabolomics and proteomic experiments, and provides community support through several web platforms. At the beginning of the next granting period, we will be supporting an initial group of 17 major users representing 23 separately funded research projects across the fields of neuroscience, including projects targeting neuropeptides, transmitters and proteins that are involved in multiple aspects of drug escalation, exposure and addiction. We also will address fundamental questions of neuron/glia communication, dendritic protein expression and neuronal plasticity. The Neuroproteomics and Neurometabolomics Center on Cell- Cell Signaling is divided into three scientific cores: Sampling and Separation, Molecular Profiling and Characterization, and Bioinformatics and Systems Biology (plus an Administrative Core). The high level of synergy between the neuroscientists and technologists affiliated with the Center ensures progress in our broad suite of supported research projects, and promises continued advancements in the knowledge of how systems of neurons interact in both the healthy nervous system and upon exposure to drugs of abuse Lastly, a series of outreach initiatives assures that our protocols and approaches are broadly available to the appropriate scientific communities.

Public Health Relevance

Literally hundreds of thousands of chemically distinct entities are present in every cell in the brain and can be modified based on exposure to drugs of abuse, and yet the technologies to measure and follow such chemical complexity are not broadly available. Our Center offers unparalleled measurement capabilities and analytical support to a broad range of drug abuse and fundamental science projects ensuring their success.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Center Core Grants (P30)
Project #
5P30DA018310-13
Application #
9069766
Study Section
Special Emphasis Panel (ZDA1)
Program Officer
Rapaka, Rao
Project Start
2004-08-23
Project End
2019-05-31
Budget Start
2016-06-01
Budget End
2017-05-31
Support Year
13
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Green, Daniel J; Huang, Rong-Chi; Sudlow, Leland et al. (2018) cAMP, Ca2+, pHi, and NO Regulate H-like Cation Channels That Underlie Feeding and Locomotion in the Predatory Sea Slug Pleurobranchaea californica. ACS Chem Neurosci 9:1986-1993
Rodriguez-Zas, Sandra L; Wu, Cong; Southey, Bruce R et al. (2018) Disruption of microglia histone acetylation and protein pathways in mice exhibiting inflammation-associated depression-like symptoms. Psychoneuroendocrinology 97:47-58
Do, Thanh D; Ellis, Joseph F; Neumann, Elizabeth K et al. (2018) Optically Guided Single Cell Mass Spectrometry of Rat Dorsal Root Ganglia to Profile Lipids, Peptides and Proteins. Chemphyschem 19:1180-1191
Atkins Jr, Norman; Ren, Shifang; Hatcher, Nathan et al. (2018) Functional Peptidomics: Stimulus- and Time-of-Day-Specific Peptide Release in the Mammalian Circadian Clock. ACS Chem Neurosci 9:2001-2008
Tai, Hua-Chia; Checco, James W; Sweedler, Jonathan V (2018) Non-targeted Identification of D-Amino Acid-Containing Peptides Through Enzymatic Screening, Chiral Amino Acid Analysis, and LC-MS. Methods Mol Biol 1719:107-118
Davis, Roderick G; Park, Hae-Min; Kim, Kyunggon et al. (2018) Top-Down Proteomics Enables Comparative Analysis of Brain Proteoforms Between Mouse Strains. Anal Chem 90:3802-3810
Qi, Meng; Philip, Marina C; Yang, Ning et al. (2018) Single Cell Neurometabolomics. ACS Chem Neurosci 9:40-50
Neumann, Elizabeth K; Comi, Troy J; Spegazzini, Nicolas et al. (2018) Multimodal Chemical Analysis of the Brain by High Mass Resolution Mass Spectrometry and Infrared Spectroscopic Imaging. Anal Chem 90:11572-11580
Yang, Ning; Anapindi, Krishna D B; Rubakhin, Stanislav S et al. (2018) Neuropeptidomics of the Rat Habenular Nuclei. J Proteome Res 17:1463-1473
Tillmaand, Emily G; Sweedler, Jonathan V (2018) Integrating Mass Spectrometry with Microphysiological Systems for Improved Neurochemical Studies. Microphysiol Syst 2:

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