Protein Science and

RTI International provides comprehensive analysis and proteomics profiling using state-of-the-art instrumentation. Our research activities include protein identification, mapping, characterization of sites of protein modification, and use of label-free and stable-isotope-labeled differential proteomics approaches for unsupervised protein target discovery and validation. We use subcellular fractionation, enrichment, and targeted multiple reaction monitoring (MRM) approaches to characterize subproteome, post- translational modifications, and protein binding partners.

Protein sciences and proteomics measure the expression, material, including bacterial and mammalian cultures, post-translational state, and biological function of , serum, plasma, saliva, and both fresh and formalin-fixed allowing us to derive detailed information about the paraffin-embedded tissues. molecular of the living cell and the organism. Our protein science and proteomics laboratory supports Approach and Capabilities several sample preparation methods, such as high- abundant-serum-protein depletion; membrane isolation; RTI applies proteomics-based approaches in multiple lipid-raft isolation and mitochondrial isolation; and scientific disciplines, including toxicology, drug discovery, enrichment of phosphopeptides, glycol-proteins, and and molecular . For example, we identified and palmitoylated proteins. We support labeled differential validated a novel role of proteasome in the activation of proteomics analysis such as SILAC (stable isotope labeling extracellular regulatory . of cell culture) and iTRAQ technologies and label-free In addition to broad-spectrum proteomics, we use targeted differential proteomics analysis for both gel-based and proteomics to investigate subcellular and gel-free samples using high-resolution as the generate the highest quality data relevant to the biological mass analyzer. Additional research activities include question. By employing different subcellular fractionation characterization of a purified protein or , protein- and enrichment techniques, we can characterize protein interaction mapping, and mapping. subproteome or post-translational modifications. For example, we use biotin-acyl chemistry to selectively enrich and profile palmitoylated membrane proteins.

We have also performed large-scale studies using 2-D , , target protein quantification and identification, and post-translational modification characterization on a variety of starting

www.rti.org Protein Science and Proteomics

Border, M.B., S. Schwartz, J. Carlson, C.F. Dibble, H. Kohltfarber, S. Offenbacher, J.B. Buse, and S. Bencharit. (2012). Exploring salivary proteomes in edentulous patients with type 2 diabetes. Molecular BioSystems 8(4), 1304–1310.

Merrick, A.B., S. Dhungana, J.G. Williams, J.J. Aloor, S. Peddada, K.B. Tomer, and M.B. Fessler. (2011). Proteomic profiling of S-acylated macrophage proteins identifies a role for palmitoylation in mitochondrial targeting of phospholipid scramblase 3. Molecular and Cellular Proteomics 10, 1–13.

Dhungana, S., B.A. Merrick, K.B. Tomer, and M.B. Fessler. (2009). Quantitative proteomic analysis of macrophage rafts reveals compartmentalized activation of the proteasome Instrumentation and Informatics and of proteasome-mediated ERK activation in response Our instrumentation capabilities include high-resolution to lipopolysaccharide. Molecular and Cellular Proteomics 8, platforms, high-throughput discovery 201–213. proteomics platforms, and quantitative targeted proteomics Dhungana, S., J.G. Williams, M.B. Fessler, and K.B. Tomer. platforms. The workflow of our protein (2009). Epitope mapping by of antigen— sciences and proteomics pipeline is supported by MASCOT, complexes. Invited book chapter. Pp. 87–110 in Methods in SEQUEST, and X!-Tandem for database searches and by Molecular Biology, Epitope Mapping Protocols 524. Edited by Scaffold and ProteoIQ for data processing and compilation. U. Reineke and M. Schutkowski. Clifton, NJ: Humana Press. The GeneGo pathway mapping tool is available to compile differential proteomics data and determine the target protein Dhungana, S., M.B. Fessler, and K.B. Tomer. (2009). Epitope or pathway. Our protein sciences and proteomics program mapping by differential chemical modification of antigens. emphasizes the importance of sample preparation, analytical Invited book chapter, Pp. 119–134 in Methods in Molecular data collection, and proper bioinformatics distillation of Biology, Epitope Mapping Protocols 524. Edited by U. Reineke analytical data to minimize false discovery rates. and M. Schutkowski. Clifton, NJ: Humana Press.

Selected Publications and Presentations More Information Bencharit, S., S. Baxter, J. Carlson, W.C. Byrd, M.V. Mayo, Suraj Dhungana, PhD M.B. Border, H. Kohltfarber, E. Urrutia, I. Saldarriaga, E.L. Systems and Translational Sciences 919.541.6601 Howard-Williams, S. Offenbacher, M.C. Wu, and J.B. Buse. [email protected] (2013). Salivary proteins associated with hyperglycemia in RTI International diabetes: A proteomic analysis. Molecular BioSystems 9(11), 3040 E. Cornwallis Road, PO Box 12194 2785–2797. Research Triangle Park, NC 27709-2194 USA Carlson, J., S.A. Baxter, D. Dreau, and I.V. Nesmelova. (2013). RTI 8816 0314 The heterodimerization of platelet-derived chemokines. Biochimica et Biophysica Acta—Proteins and Proteomics 1834(1), 158–168.

RTI International is one of the world’s leading research institutes, dedicated to improving the human condition by turning knowledge into practice. Our staff of more than 3,700 provides research and technical services to governments and businesses in more than 75 countries in the areas of health and pharmaceuticals, education and training, surveys and statistics, advanced technology, international development, economic and social policy, energy and the environment, and laboratory testing and chemical analysis. For more information, visit www.rti.org. RTI International is a trade name of Research Triangle Institute.