This proposal describes a program for developing multidimensional analytical techniques for the analysis of complex biological mixtures that are extracted from Drosophila melanogaster as a function of the age of the organism. Preliminary data show that a new gas-phase ion mobility/time-of-flight mass spectrometry technique can be coupled to other separation techniques in order to separate and characterize complex mixtures of tryptic peptides obtained from digestion of soluble proteins. The gas-phase separation reduces spectral congestion and chemical noise associated with mass spectrometry alone, provides additional information about charge state and amino acid composition, and allows a parallel approach for obtaining fragmentation data (an important factor for assigning peptide sequence and identifying proteins). This proposal describes the further advancement of these technologies and their applications to the emerging field of proteomics. An aggressive plan that aims to map the proteome for the fundamental model Drosophila organism is proposed. This existence of a detailed proteomic map for this system is an important scientific step that will allow a range of genetic models to be investigated in detail. These models are chosen to display characteristics of diseased states (e.g., neurodegenerative conditions) for which genetic studies in humans are intractable.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG024547-03
Application #
7224853
Study Section
Special Emphasis Panel (ZRG1-BECM (01))
Program Officer
Velazquez, Jose M
Project Start
2005-05-15
Project End
2009-04-30
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
3
Fiscal Year
2007
Total Cost
$249,005
Indirect Cost
Name
Indiana University Bloomington
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
Atlasevich, Natalya; Holliday, Alison E; Valentine, Stephen J et al. (2012) Collisional activation of [14Pro+2H]2+ clusters: chiral dependence of evaporation and fission processes. J Phys Chem B 116:7644-51
Kurulugama, Ruwan T; Nachtigall, Fabiane M; Valentine, Stephen J et al. (2011) Overtone mobility spectrometry: part 4. OMS-OMS analyses of complex mixtures. J Am Soc Mass Spectrom 22:2049-60
Li, Zhiyu; Valentine, Stephen J; Clemmer, David E (2011) Complexation of amino compounds by 18C6 improves selectivity by IMS-IMS-MS: application to petroleum characterization. J Am Soc Mass Spectrom 22:817-27
Lee, Sunyoung; Ewing, Michael A; Nachtigall, Fabiane M et al. (2010) Determination of cross sections by overtone mobility spectrometry: evidence for loss of unstable structures at higher overtones. J Phys Chem B 114:12406-15
Liu, Xiaoyun; Afrane, Mary; Clemmer, David E et al. (2010) Identification of Chlamydia trachomatis outer membrane complex proteins by differential proteomics. J Bacteriol 192:2852-60
Robinson, Rena A S; Kellie, John F; Kaufman, Thomas C et al. (2010) Insights into aging through measurements of the Drosophila proteome as a function of temperature. Mech Ageing Dev 131:584-90
Merenbloom, Samuel I; Glaskin, Rebecca S; Henson, Zachary B et al. (2009) High-resolution ion cyclotron mobility spectrometry. Anal Chem 81:1482-7
Valentine, Stephen J; Stokes, Sarah T; Kurulugama, Ruwan T et al. (2009) Overtone mobility spectrometry: part 2. Theoretical considerations of resolving power. J Am Soc Mass Spectrom 20:738-50
Xun, Zhiyin; Kaufman, Thomas C; Clemmer, David E (2009) Stable isotope labeling and label-free proteomics of Drosophila parkin null mutants. J Proteome Res 8:4500-10
Kurulugama, Ruwan T; Nachtigall, Fabiane M; Lee, Sunyoung et al. (2009) Overtone mobility spectrometry: part 1. Experimental observations. J Am Soc Mass Spectrom 20:729-37

Showing the most recent 10 out of 29 publications