Overall goals of this research are two in number;(1) to continue the development of mass spectrometry instrumentation, software, and methodology for the identification and sequence analysis of proteins in complex mixtures at the attomole/femtomole level and (2) to employ the technology to solve structural problems at the cutting edge health related biological research.
Specific Aims are 5 in number: (1) to develop instrumentation, software, and chemistry that will facilitate the use of electron transfer dissociation (ETD) mass spectrometry for the characterization, differential display, and quantitation of intact proteins (and their posttranslational modifications) expressed in two or more different cell trypes or states;(2) to decipher the histone code, patterns of post-translational modifications on histone variants that regulate transcription, gene and chromosome silencing, cellular differentiation and reprogramming, DMA damage/repair and chromosome condensation in apoptosis;(3) to immunopurify and characterize proteins that are posttranslationally modified by polyglutamylation;(4) to characterize novel antimicrobial, alpha- defensins/cryptdins and related cysteine-rich sequence (CRS) peptides by ETD mass spectrometry, and (5) to indentify components of kinetochore, the large multiprotein structure that coordinates chromosome segregation during cell division. Continued development of novel mass spectrometry technology is highly relevant to public health because it facilitates identification of proteins and their post-translational modifications that are uniquely expressed as a function of cellular perturbations such as disease, injury, drug treatment, hormone regulation, genetics and environmental impact. Enzymes responsible for introducing and removing post-translational modifications along with protein binding partners that recognize the post- translational modifications are implicated in many types diseases including cancer and autoimmune disorders and, thus, are targets for development of both disease diagnostics and candidates for therapeutic intervention.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM037537-24
Application #
7925581
Study Section
Enabling Bioanalytical and Biophysical Technologies Study Section (EBT)
Program Officer
Edmonds, Charles G
Project Start
1987-01-12
Project End
2011-08-31
Budget Start
2010-09-01
Budget End
2011-08-31
Support Year
24
Fiscal Year
2010
Total Cost
$953,009
Indirect Cost
Name
University of Virginia
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Martínez-Turiño, Sandra; Pérez, José De Jesús; Hervás, Marta et al. (2018) Phosphorylation coexists with O-GlcNAcylation in a plant virus protein and influences viral infection. Mol Plant Pathol 19:1427-1443
Simon, Dan N; Wriston, Amanda; Fan, Qiong et al. (2018) OGT (O-GlcNAc Transferase) Selectively Modifies Multiple Residues Unique to Lamin A. Cells 7:
Malaker, Stacy A; Penny, Sarah A; Steadman, Lora G et al. (2017) Identification of Glycopeptides as Posttranslationally Modified Neoantigens in Leukemia. Cancer Immunol Res 5:376-384
Weisbrod, Chad R; Kaiser, Nathan K; Syka, John E P et al. (2017) Front-End Electron Transfer Dissociation Coupled to a 21 Tesla FT-ICR Mass Spectrometer for Intact Protein Sequence Analysis. J Am Soc Mass Spectrom 28:1787-1795
Zentella, Rodolfo; Sui, Ning; Barnhill, Benjamin et al. (2017) The Arabidopsis O-fucosyltransferase SPINDLY activates nuclear growth repressor DELLA. Nat Chem Biol 13:479-485
Stankovic, Ana; Guo, Lucie Y; Mata, João F et al. (2017) A Dual Inhibitory Mechanism Sufficient to Maintain Cell-Cycle-Restricted CENP-A Assembly. Mol Cell 65:231-246
Zhang, Lichao; English, A Michelle; Bai, Dina L et al. (2016) Analysis of Monoclonal Antibody Sequence and Post-translational Modifications by Time-controlled Proteolysis and Tandem Mass Spectrometry. Mol Cell Proteomics 15:1479-88
Bailey, Aaron O; Panchenko, Tanya; Shabanowitz, Jeffrey et al. (2016) Identification of the Post-translational Modifications Present in Centromeric Chromatin. Mol Cell Proteomics 15:918-31
Zentella, Rodolfo; Hu, Jianhong; Hsieh, Wen-Ping et al. (2016) O-GlcNAcylation of master growth repressor DELLA by SECRET AGENT modulates multiple signaling pathways in Arabidopsis. Genes Dev 30:164-76
Anderson, Lissa C; Karch, Kelly R; Ugrin, Scott A et al. (2016) Analyses of Histone Proteoforms Using Front-end Electron Transfer Dissociation-enabled Orbitrap Instruments. Mol Cell Proteomics 15:975-88

Showing the most recent 10 out of 189 publications