Mass spectrometry (MS) based protein footprinting is a new addition to structural biology tool box. The sensitivity and speed of MS provide a bridge between low resolution methods, like circular dichroism, and high resolution methods, like NMR and X-ray crystallography. Footprinting modifies proteins in biologically relevant environments. The modified peptides can be qualitatively and quantitatively analyzed by MS to generate maps of the solvent accessibility of target proteins. This view of the protein structure at the peptide level is sufficient to determine protein conformational changes introduced by the functional switch of proteins and can be investigated without limitations of purity and size. Two approaches are deuterium (hydrogen deuterium exchange, or HDX) and hydroxyl radical labeling (fast photochemical oxidation of proteins, or FPOP). Both of them can label more than half of the amino acids in biologically relevant environments. FPOP can monitor very fast events, down to a microsecond. Phenomena such as fast protein folding, conformational changes, and aggregation can now be probed. In addition, other radicals that react with specific residues will be developed. Combining HDX with MS allows much deeper investigation. Titration-based HDX will be exploited to provide protein-ligand binding affinities. Pulsed HDX will be developed to look at challenging protein aggregates such as amyloid beta (implicated in Alzheimer's Disease). Both technologies will be pushed to determine if they can provide information at the amino acid residue level.

Public Health Relevance

-Public Health Relevance. The Washington University Biomedical Mass Spectrometry Resource has a longstanding history as an active and productive citizen in the NIH Biotechnology Research Resources community. We propose to extend our mission by advancing mass spectrometry technology, development, and research, applying these discoveries to answer critical biomedical research questions, and training the next generation of researchers, towards the ultimate goal of improving public health.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Biotechnology Resource Grants (P41)
Project #
5P41GM103422-40
Application #
9199434
Study Section
Special Emphasis Panel (ZRG1-IMST-B)
Project Start
Project End
Budget Start
2017-01-01
Budget End
2017-12-31
Support Year
40
Fiscal Year
2017
Total Cost
$105,120
Indirect Cost
$36,189
Name
Washington University
Department
Type
Domestic Higher Education
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Illes-Toth, Eva; Rempel, Don L; Gross, Michael L (2018) Pulsed Hydrogen-Deuterium Exchange Illuminates the Aggregation Kinetics of ?-Synuclein, the Causative Agent for Parkinson's Disease. ACS Chem Neurosci 9:1469-1476
Johnston, Adam B; Hilton, Denise M; McConnell, Patrick et al. (2018) A novel mode of capping protein-regulation by twinfilin. Elife 7:
Ikon, Nikita; Hsu, Fong-Fu; Shearer, Jennifer et al. (2018) Evaluation of cardiolipin nanodisks as lipid replacement therapy for Barth syndrome J Biomed Res 32:107-112
Schweitzer, George G; Collier, Sara L; Chen, Zhouji et al. (2018) Loss of lipin 1-mediated phosphatidic acid phosphohydrolase activity in muscle leads to skeletal myopathy in mice. FASEB J :fj201800361R
Howard, Nicole C; Marin, Nancy D; Ahmed, Mushtaq et al. (2018) Mycobacterium tuberculosis carrying a rifampicin drug resistance mutation reprograms macrophage metabolism through cell wall lipid changes. Nat Microbiol 3:1099-1108
Li, Ke Sherry; Shi, Liuqing; Gross, Michael L (2018) Mass Spectrometry-Based Fast Photochemical Oxidation of Proteins (FPOP) for Higher Order Structure Characterization. Acc Chem Res 51:736-744
Chanthamontri, C Ken; Jordan, David; Wang, Wenjie et al. (2018) Ebola Viral Protein 35 N-terminus is a Parallel Tetramer. Biochemistry :
Turk, John; White, Tayleur D; Nelson, Alexander J et al. (2018) iPLA2? and its role in male fertility, neurological disorders, metabolic disorders, and inflammation. Biochim Biophys Acta Mol Cell Biol Lipids :
Shen, Guomin; Li, Shuang; Cui, Weidong et al. (2018) Membrane Protein Structure in Live Cells: Methodology for Studying Drug Interaction by Mass Spectrometry-Based Footprinting. Biochemistry 57:286-294
Mukherjee, Sumit; Xu, Wei; Hsu, Fong-Fu et al. (2018) Sterol methyltransferase is required for optimal mitochondrial function and virulence in Leishmania major. Mol Microbiol :

Showing the most recent 10 out of 323 publications