A modern, state-of-the-art triple quadrupole mass spectrometer, equipped with on-line HPLC capabilities, a high-throughput autosampler, and electrospray ionization (ESI) and atmospheric pressure chemical ionization (APCI) sources, for quantitative and qualitative analysis is requested. This instrument will be a vital component to support the specific aims of over 10 NIH-funded projects. The NIH-funded projects involve the measurement of a variety of molecular species, including lipids and phospholipids, cholesterol, fatty acids and triglycerides, steroids and prostaglandins, peptides, and nucleosides and nucleotides. With selected reaction monitoring (SRM) and multiple reaction monitoring (MRM) using the triple quadrupole analyzer, excellent precision and sensitive limits of detection (LOD) from complex matrices can be achieved that is unparalleled by most mass analyzers. Sub-ng/mL limits of quantification (LOQ) with internal standards can be achieved for many compounds using triple quadrupole analyzers. For detecting protein biomarkers of disease, the MRM functionality of the triple quadrupole MS allows for monitoring multiple proteins simultaneously with low coefficients of variation (CVs) in a single experiment. Thus, studies that focus on the discovery of novel protein biomarkers of disease would benefit from the MRM-based methodology (with enrichment of specific target, low abundance peptides) for validation of candidate or proposed biomarkers. The proposed LC-triple quadrupole mass spectrometer system will be supported and administered by the UCLA Molecular Instrumentation Center (MIC), a campus-wide, integrated facility formed to enhance the accessibility of existing shared, sophisticated instrumentation facilities to the broader research community at the institution. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR024605-01
Application #
7389810
Study Section
Special Emphasis Panel (ZRG1-BCMB-M (30))
Program Officer
Tingle, Marjorie
Project Start
2007-09-20
Project End
2008-09-19
Budget Start
2007-09-20
Budget End
2008-09-19
Support Year
1
Fiscal Year
2007
Total Cost
$423,773
Indirect Cost
Name
University of California Los Angeles
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
He, Cuiwen H; Black, Dylan S; Allan, Christopher M et al. (2017) Human COQ9 Rescues a coq9 Yeast Mutant by Enhancing Coenzyme Q Biosynthesis from 4-Hydroxybenzoic Acid and Stabilizing the CoQ-Synthome. Front Physiol 8:463
Xie, Letian X; Williams, Kevin J; He, Cuiwen H et al. (2015) Resveratrol and para-coumarate serve as ring precursors for coenzyme Q biosynthesis. J Lipid Res 56:909-19
Allan, Christopher M; Awad, Agape M; Johnson, Jarrett S et al. (2015) Identification of Coq11, a new coenzyme Q biosynthetic protein in the CoQ-synthome in Saccharomyces cerevisiae. J Biol Chem 290:7517-34
Nguyen, Theresa P T; Casarin, Alberto; Desbats, Maria Andrea et al. (2014) Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis. Biochim Biophys Acta 1841:1628-38
He, Cuiwen H; Xie, Letian X; Allan, Christopher M et al. (2014) Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants. Biochim Biophys Acta 1841:630-44
Gerling, Kimberly A; Rezayee, Nomaan M; Rheingold, Arnold L et al. (2014) Synthesis and structures of bis-ligated zinc complexes supported by tridentate ketoimines that initiate L-lactide polymerization. Dalton Trans 43:16498-508
Buehler, Daniel C; Marsden, Matthew D; Shen, Sean et al. (2014) Bioengineered vaults: self-assembling protein shell-lipophilic core nanoparticles for drug delivery. ACS Nano 8:7723-32
Rezayee, Nomaan M; Gerling, Kimberly A; Rheingold, Arnold L et al. (2013) Synthesis and structures of tridentate ketoiminate zinc complexes bearing trifluoromethyl substituents that act as L-lactide ring opening polymerization initiators. Dalton Trans 42:5573-86
Ashraf, Shazia; Gee, Heon Yung; Woerner, Stephanie et al. (2013) ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. J Clin Invest 123:5179-89
Gasser, David L; Winkler, Cheryl A; Peng, Min et al. (2013) Focal segmental glomerulosclerosis is associated with a PDSS2 haplotype and, independently, with a decreased content of coenzyme Q10. Am J Physiol Renal Physiol 305:F1228-38

Showing the most recent 10 out of 23 publications