Hongwei Xie, Getiria Onsongo, Jonathan Popko, Ebbing P. de Jong,
Jing Cao, John V. Carlis, Robert J. Griffin, Nelson L. Rhodus and Timothy J. Griffin.
“ Proteomics Analysis of Cells in Whole Saliva from Oral Cancer Patients via Value-added
Three-dimensional Peptide Fractionation and Tandem Mass Spectrometry ” .
In journal Molecular & Cellular Proteomics 2008, Mar; 7(3): 486-98.
- Fulltext: Link to article in PubMed
- Summary of main contribution:
- This paper presents a novel proteomics methods used to characterize for the first time cells contained
in whole saliva from patients diagnosed with oral squamous cell cell carcinoma. Our results confirm the
potential of analyzing cells in whole saliva using our proteomics method to detect salivary markers of oral
cancer and possibly other conditions of the oral cavity.
Ebbing P. de Jong, Hongwei Xie, Getiria Onsongo, Matthew D. Stone, Xiao-Bing Chen,
Joel A. Kooren, Eric W. Refsland, Robert J. Griffin, Frank G. Ondrey, Baolin Wu, Chap T. Le, Nelson L. Rhodus,
John V. Carlis and Timothy J. Griffin.
“ Quantitative Proteomics Reveals Myosin and Actin as Promising Saliva Biomarkers for Distinguishing
Pre-Malignant and Malignant Oral Lesions ” .
In journal PLoS ONE 2010, June 17; 5(6): e11148.
- Fulltext: Link to article in PubMed
- Summary of main contribution:
- In this first-of-its kind study we used advanced mass spectrometry-based quantitative proteomics analysis
to identify actin and myosin as promising saliva biomarkers for distinguishing
pre-malignant and malignant oral lesions. We prioritize candidate biomarkers via bioinformatics and validate
actin and myosin using western blotting. We show abundances for salivary actin and
myosin distinguish oral lesion types with sensitivity and specificity rivaling other non-invasive oral
cancer tests.
Sricharan Bandhakavi, Matthew D. Stone, Getiria Onsongo, Susan K. Van Riper
and Timothy J. Griffin.
“ A Dynamic Range Compression and Three-Dimensional Peptide Fractionation Analysis Platform
Expands Proteome Coverage and the Diagnostic Potential of Whole Saliva ” .
In journal of Proteome Research 2009, Dec; 8(12): 5590-5600.
- Fulltext: Link to article in PubMed
- Summary of main contribution:
- The large dynamic range of protein abundance in saliva hinders a comprehensive identification of
proteins limiting its full diagnostic potential. In this work we use an analysis platform that coupled
hexapeptide libraries for dynamic range compression (DRC) with three-dimensional (3D) peptide fractionation.
This approach identified 2340 proteins in whole saliva and represents the largest saliva proteomic
dataset generated using a single platform analysis. These results expand the potential for whole saliva in
health monitoring/diagnostics and provide a general platform for improving proteomic coverage of complex
biological fluids.
Matthew D. Stone, Rick M. Odland, Thomas McGowan, Getiria Onsongo, Chaunning Tang,
Nelson L. Rhodus, Pratik Jagtap, Sricharan Bandhakavi and Timothy J. Griffin.
“ Novel In Situ Collection of Tumor Interstitial Fluid from Head and Neck Squamous Carcinoma
Reveals a Unique Proteome with Diagnostic Potential ” .
In journal Clin. Proteom. 2010, Epub 25 July.
- Fulltext: Link to article in SpringerLink
- Summary of main contribution:
- Tumors lack normal drainage of secreted fluids and consequently build up tumor interstitial fluid (TIF).
Unlike other bodily fluids, TIF likely contains a high proportionof tumor-specific proteins with potential
as biomarkers. We evaluate a novel technique using a unique ultrafiltration catheter for in situ collection of
TIF and used it to generate the first catalog of TIF proteins from head and neck squamous cell carcinoma (HNSCC).
Elizabeth Shoop, Paulo Casaes, Getiria Onsongo, Lisa Lesnett,
Erla Osk Petursdottir, Edward Kofi Yeboah Donkor, Dennis Tkach and Michael Cosimini.
“ Data exploration tools for the Gene Ontology database ” .
In journal Bioinformatics. 2004, Dec 12; 20(18):3442-54.
- Fulltext: Link to article in PubMed
- Summary of main contribution:
- We develop two new tools (GoGet and GoView) built as part of an extensible web application system based
on Java 2 Enterprise Edition technology that improve the ability of biologists to ask biologically interesting
questions of the Gene Ontology (GO) database. GoGet has a user interface that enables users to ask biologically
interesting questions such as “ What are the DNA binding proteins involved in DNA repair, but not
in DNA replication? ” . GoView enables users to explore the large directed acyclic graph structure
of the ontologies in the GO database.
Sara Mullen and Getiria Onsongo.
“ Decentralized agent-based underfrequency load shedding ” .
In journal Integrated Computer-Aided Engineering accepted, 2010.
- Fulltext: Will be made available as soon as the article is published.
- Summary of main contribution:
- As part of the transition to a smart grid efforts are being made to decentralize control of electric power
systems and modernize protection schemes that are currently in use. One specific application of distributed
control is underfrequency load shedding (UFLS), which is used to restore the load/generation balance in a power
system following unusual disturbances e.g., loss of a generator. UFLS is currently performed by automatically
shedding preset amounts of load without situational awareness. We develop an agent-based UFLS scheme that allows
for an adaptive response to emergency loading conditions. We show the amount of load shed using this new scheme
is reduced considerably compared to a traditional UFLS scheme.
Sricharan Bandhakavi, Young-Mi Kim, Seung-Hyun Ro, Hongwei Xie, Getiria Onsongo,
Chang-Bong Jun, Do-Hyung Kim and Timothy J. Griffin.
“ Quantitative Nuclear Proteomics Identifies mTOR Regulation of DNA Damage Response ” .
In journal Molecular & Cellular Proteomics 2010, Feb; 9(2): 403-14.
- Fulltext: Link to article in PubMed
- Summary of main contribution:
- Cellular nutritional and energy status regulates a wide range of nuclear processes important for cell
growth, survival and metabolic homeostasis. Mammalian target of rapamycin (mTOR) plays a key role in the
cellular responses to nutrients. However, the nuclear processes governed mTOR have not been clearly defined.
Using mass spectrometry techniques, we performed quantitative proteomics analysis to identify nuclear processes
in human cells under control of mTOR. Results reveal a novel functional link between mTOR and DNA Damage Response
(DDR) pathways in the nucleus potentially operating as a survival mechanism against unfavorable growth conditions.