Welcome to our Center!
Our P30 Center, funded by the National Institute on Drug Abuse (NIDA), provides proteomics, metabolomics and bioinformatics technologies to biological collaborators at the University of Illinois at Urbana-Champaign, and to members of the neuroscience community at other institutions in the United States and throughout the world. Our Center is built around the overarching theme of cell-cell signaling to advance state-of-the-art proteomics/metabolomics technologies focused on the study of addiction mechanisms in the central nervous system.
Why focus on cell-cell signaling? Intercellular signaling plays a crucial role in the organization and coordination of biological systems. A surprisingly large number of physicochemically and structurally distinct molecules are involved in communication among the cells of the brain, with more being discovered each year. These molecules range in size from the small nitric oxide molecule to large >100 kDa heavily post-translationally modified proteins. In addition, these are the endogenous molecules many of the drugs of abuse mimic in terms of receptor binding and other functions. Therefore, these molecules are particularly relevant in drug abuse research and present high-value targets for pharmacological intervention.
Services are provided to support our collaborators' projects via three synergistic scientific research cores: Sampling & Separation, Molecular Profiling & Characterization, and Bioinformatics, Data Analytics & Predictive Modeling. The Administrative core offers the support necessary to promote and maintain innovative scientific interactions while facilitating interactions among the three individual research cores and Center collaborators. Interested in collaborating with us? Find out how.
Learn more about our cores....
Our Center's Goals include:
Providing metabolomics / peptidomics / proteomics measurement capabilities and bioinformatics services to the Illinois, national and international neuroscience communities working on both fundamental neuroscience research and the study of drug addiction mechanisms.
Discovering the functional roles of metabolites, peptides and proteins in cell-cell signaling, memory, behavior and addiction.
Creating improved MS-based molecular characterization technologies to enable new investigations of cell-cell signaling.
Integrating proteomic and transcriptomic information in support of more accurate molecular identification and molecular network inference using systems biology approaches.
Leslie Sombers is an Associate Professor of Analytical Chemistry and University Faculty Scholar at North Carolina State University. Her area of interest and expertise is in development, characterization, and application of electroanalytical techniques to study real-time neurochemical fluctuations in biological systems ranging from single cells in culture to the brain of an awake, behaving animal.
Sombers works with us on evaluating opioid peptide secretion in the striatum and the ventral tegmental area in response to electrical stimulation and correlation of secreted peptide profiles to the strength of an electrical stimulus. Using fast-scan cyclic voltammetry and carbon-fiber microelectrodes to stimulate and monitor select peptide secretion from brain slices, Sombers then relies on our unique small-scale solid phase extraction sampling of cerebro-spinal fluid in the vicinity of the brain slice to collect peptides for follow-up peptidomic analysis using our mass spectrometry methods. This integrative, multi-modal analytical approach validates electrochemically detected peptides and reveals potential unexpected peptides not picked up by electrochemical detection. Sombers' study is a critical step toward elucidating how the release and clearance dynamics of several neuropeptides and small molecules underlie discrete aspects of motivated behavior. It will enable direct quantification of endogenous opioid peptides in live brain tissue to clarify outstanding questions regarding the fundamental nature of endogenous opioid peptide signaling and help establish the precise role that these molecules play in devastating substance abuse disorders.
Exploring Exercise- and Context-Induced Peptide Changes in Mice by Quantitative Mass Spectrometry, S.E. Dowd, M.L. Mustroph, E.V. Romanova, B.R. Southey, H. Pinardo, J.S. Rhodes, J.V. Sweedler, ACS Omega 3, 2018, 13817–13827. [Selected as an ACS Editors' Choice open access article.]
Multimodal Chemical Analysis of the Brain by High Mass Resolution Mass Spectrometry and Infrared Spectroscopic Imaging, E.K. Neumann, T.J. Comi, N. Spegazzini, J.W. Mitchell, S.S. Rubakhin, M.U. Gillette, R. Bhargava, J.V. Sweedler, Anal. Chem. 90, 11572–11580.
Disruption of Microglia Histone Acetylation and Protein Pathways in Mice Exhibiting Inflammation-Associated Depression-Like Symptoms, S.L. Rodriguez-Zas, C. Wu, B.R. Southey, J.C. O’Connor, S.E. Nixon, R. Garcia, C. Zavala, M. Lawson, R.H. McCusker, E.V. Romanova, J.V. Sweedler, K.W. Kelley, R. Dantzer, Psychoneuroendocrinology 97, 2018, 47–58.
Molecular and Physiological Characterization of a D-Amino Acid-Containing Neuropeptide Receptor, J.W. Checco, G. Zhang, W. Yuan, K. Yu, S. Yin, R.H. Roberts-Galbraith, P.M. Yau, E.V. Romanova, J. Jing, J.V. Sweedler, ACS Chem. Biol. 13, 2018,1343–1352.
Neuropeptidomics of the Rat Habenular Nuclei, N. Yang, K.D.B. Anapindi, S.S. Rubakhin, P. Wei, Q. Yu, L. Li, P.J. Kenny, J.V. Sweedler, J. Proteome Res. 17, 2018, 1463–1473.