? Overall Advances in high-throughput phenotyping and molecular characterization technologies have had profound impacts on biological research. However, it is frequently difficult, for example, to study the functional consequences of genetic changes because of the lack of suitable analytical technologies to define the functional cellular state. Mass spectrometry (MS) is presently the most powerful approach for quantifying the molecular changes that arises from altered gene expression, but limitations have prevented it from being a routine and broadly available tool. Specifically, the sensitivity, throughput and precision of proteomics measurements are significantly less than other high-throughput technologies that are driving major advances in modern biology (e.g. sequencing and high-content imaging). In this renewal the Proteomics Resource has the goal of broadly impacting biomedical research by providing the abilities to: obtain high quality data from at least 10- to 100- fold smaller samples, produce much more comprehensive quantitative measurements, improve coverage of low abundance components such as problematic peptide isomers and post translational modifications, and enable the analysis of far larger sample sets than presently practical by providing large increases in measurement throughput. We will address the key deficiencies of proteomics using new Structures for Lossless Ion Manipulations (SLIM) ion mobility (IM)-MS based technologies that will vastly increase proteomic sample throughput as well as provide improved reproducibility, sensitivity, accuracy of quantification and coverage of proteomics measurements. These advances will be complemented by innovative approaches for rapid nanoliter scale robotic processing of much smaller samples than presently feasible, and include analyses of important functional `sub-proteomes' (e.g. phosphoproteomics and activity-based proteomics samples). The robotic sample processing will provide throughput matching the speed of the SLIM IM-MS platform. These advances will occur in conjunction with algorithmic and software developments needed to handle the SLIM IM-MS platform data flow and bioinformatics for obtaining biological insights from these data. In combination, our work will lead to the rapid implementation of the new capabilities through their application to a set of challenging biomedical projects. The developments will be disseminated to the broader community by both conventional (e.g. workshops and training activities) and direct approaches that include working directly to `seed' the new technology in a number of outside research laboratories with expertise in developing and implementing biomedical technologies, and also helping to facilitate commercial implementations from a number of vendors spanning multiple MS platform types. Our project will result in broad and impactful initial applications of advanced proteomics capabilities, and effective dissemination of these technologies by the end of this final renewal of the Resource.

Public Health Relevance

? Overall The Resource will address key present deficiencies of proteomics and enable large impacts across broad areas of biomedical research. Specifically, the advances will enable mass spectrometry-based proteomics measurements using much smaller protein samples than previously practical, providing greatly increased sample throughput and data of higher quality (including improved reproducibility and greater protein coverage). The Resource will accomplish this through the development, initial application, and dissemination of platform advances together with supporting software and bioinformatics tools that will enable a wide range of previously impractical lines of biomedical research, while also assuring their broad and sustained availability.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Biotechnology Resource Grants (P41)
Project #
5P41GM103493-18
Application #
9988423
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Sakalian, Michael
Project Start
2003-09-15
Project End
2023-07-31
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
18
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Battelle Pacific Northwest Laboratories
Department
Type
DUNS #
032987476
City
Richland
State
WA
Country
United States
Zip Code
99352
Prabhakaran, Aneesh; Hamid, Ahmed M; Garimella, Sandilya V B et al. (2018) A Hybrid Constant and Oscillatory Field Ion Mobility Analyzer Using Structures for Lossless Ion Manipulations. J Am Soc Mass Spectrom 29:342-351
Stevens, Susan L; Liu, Tao; Bahjat, Frances Rena et al. (2018) Preconditioning in the Rhesus Macaque Induces a Proteomic Signature Following Cerebral Ischemia that Is Associated with Neuroprotection. Transl Stroke Res :
Chouinard, Christopher D; Nagy, Gabe; Webb, Ian K et al. (2018) Improved Sensitivity and Separations for Phosphopeptides using Online Liquid Chromotography Coupled with Structures for Lossless Ion Manipulations Ion Mobility-Mass Spectrometry. Anal Chem 90:10889-10896
Petyuk, Vladislav A; Chang, Rui; Ramirez-Restrepo, Manuel et al. (2018) The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease target. Brain 141:2721-2739
Rodland, Karin D; Piehowski, Paul; Smith, Richard D (2018) Moonshot Objectives: Catalyze New Scientific Breakthroughs-Proteogenomics. Cancer J 24:121-125
Yi, Lian; Shi, Tujin; Gritsenko, Marina A et al. (2018) Targeted Quantification of Phosphorylation Dynamics in the Context of EGFR-MAPK Pathway. Anal Chem 90:5256-5263
Kyle, Jennifer E; Aly, Noor; Zheng, Xueyun et al. (2018) Evaluating lipid mediator structural complexity using ion mobility spectrometry combined with mass spectrometry. Bioanalysis 10:279-289
Zhu, Ying; Zhao, Rui; Piehowski, Paul D et al. (2018) Subnanogram proteomics: impact of LC column selection, MS instrumentation and data analysis strategy on proteome coverage for trace samples. Int J Mass Spectrom 427:4-10
Menachery, Vineet D; Schäfer, Alexandra; Burnum-Johnson, Kristin E et al. (2018) MERS-CoV and H5N1 influenza virus antagonize antigen presentation by altering the epigenetic landscape. Proc Natl Acad Sci U S A 115:E1012-E1021
Khanova, Elena; Wu, Raymond; Wang, Wen et al. (2018) Pyroptosis by caspase11/4-gasdermin-D pathway in alcoholic hepatitis in mice and patients. Hepatology 67:1737-1753

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