Currently, the UCSF Mass Spectrometry Facility is equipped with two PerSeptive Biosystems Voyager and one AutoSpec MALDI instruments. Optimization of methods of sample preparation and laser configuration would enable the most efficient and productive use of the available instruments. Sensitivity enhancement would improve the data quality for researchers. Comparison of the two Voyager instruments has established equivalent sensitivity for both in linear and reflectron modes using standard dried droplet matrix preparation on a cze standard with chca matrix. The minimum requirement for detection with this method is from 10 to 100 fmol. To improve upon these limits, a protocol involving nitrocullulose/chca mixtures is being tested and has been demonstrated to allow detection at low fmol levels, with reproducibility in question at lower levels. Increased laser focus has been tested without improvement, but needs to be tested in conjunctuion with the nitrocullulose/chca sample preparation techniques. Usefulness for lab samples such as in gel digests will be evaluated once clear improvements on standards have been demonstrated. A second area of development is the use of alternative matrices and comparison of the UV and IR laser for MALDI. IR laser in conjunction with suitable matrices has been shown to reduce metastable decay of sialated and phosphorylated peptides. However, difficulties with laser stability and sample crystallization impede widespread use of the technique. Thus, development of appropriate sample preparation methods and optimal laser settings on the Voyager DE-STR IR system will be continued. Samples currently of interest to the group will take priority, such as sulfated peptides.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001614-18
Application #
6120205
Study Section
Project Start
1999-03-01
Project End
2000-02-29
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
18
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
MacRae, Andrew J; Mayerle, Megan; Hrabeta-Robinson, Eva et al. (2018) Prp8 positioning of U5 snRNA is linked to 5' splice site recognition. RNA 24:769-777
Katsuno, Yoko; Qin, Jian; Oses-Prieto, Juan et al. (2018) Arginine methylation of SMAD7 by PRMT1 in TGF-?-induced epithelial-mesenchymal transition and epithelial stem-cell generation. J Biol Chem 293:13059-13072
Sahoo, Pabitra K; Smith, Deanna S; Perrone-Bizzozero, Nora et al. (2018) Axonal mRNA transport and translation at a glance. J Cell Sci 131:
Tran, Vy M; Wade, Anna; McKinney, Andrew et al. (2017) Heparan Sulfate Glycosaminoglycans in Glioblastoma Promote Tumor Invasion. Mol Cancer Res 15:1623-1633
Liu, Tzu-Yu; Huang, Hector H; Wheeler, Diamond et al. (2017) Time-Resolved Proteomics Extends Ribosome Profiling-Based Measurements of Protein Synthesis Dynamics. Cell Syst 4:636-644.e9
Bikle, Daniel D (2016) Extraskeletal actions of vitamin D. Ann N Y Acad Sci 1376:29-52
Twiss, Jeffery L; Fainzilber, Mike (2016) Neuroproteomics: How Many Angels can be Identified in an Extract from the Head of a Pin? Mol Cell Proteomics 15:341-3
Cil, Onur; Phuan, Puay-Wah; Lee, Sujin et al. (2016) CFTR activator increases intestinal fluid secretion and normalizes stool output in a mouse model of constipation. Cell Mol Gastroenterol Hepatol 2:317-327
Posch, Christian; Sanlorenzo, Martina; Vujic, Igor et al. (2016) Phosphoproteomic Analyses of NRAS(G12) and NRAS(Q61) Mutant Melanocytes Reveal Increased CK2? Kinase Levels in NRAS(Q61) Mutant Cells. J Invest Dermatol 136:2041-2048
Julien, Olivier; Zhuang, Min; Wiita, Arun P et al. (2016) Quantitative MS-based enzymology of caspases reveals distinct protein substrate specificities, hierarchies, and cellular roles. Proc Natl Acad Sci U S A 113:E2001-10

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