The Mass Spectrometry (MS) Shared Resource offers a wide range of analytical capabilities to support the needs of UTHSCSA investigators and others in the nearby research community. The core facility is directed by Susan T. Weintraub, Ph.D., and is located on the main UTHSCSA campus. The facility includes the following instrumentation: 1) Finnigan LCQ ion trap mass spectrometer capable of nanospray and micro-HPLC-ESI/MSn measurements, used in conjunction with a Michrom BioResources MAGIC 2002 micro-HPLC; 2) Applied Biosystems Voyager DE-STR MALDI-TOF/MS; 3) Applied Biosystems Voyager Elite MALDI-TOF/MS; and 4) Finnigan SSQ700 quadrupole mass spectrometer which is able to perform GC/MS and direct probe analyses using electron impact and chemical ionization with positive and negative ion detection. A satellite facility of the MS Core has been established at the Institute of Biotechnology within the Texas Research Park, which is located 20 miles from the UTHSCSA main campus. The satellite unit encompasses a 200 sq. ft. laboratory and includes the following instrumentation: 1) an Applied Biosystems Voyager DE-PRO Biospectrometry workstation, consisting of a high performance integrated MALDI-TOF mass spectrometer, a SymBiot I Sample Workstation, and a PS-1 sample handling and data analysis system; and 2) a Thermo Finnigan integrated LC/MS system consisting of a Surveyor HPLC coupled in-line with a Finnigan LCQ DUO ion trap mass spectrometer with MS/MS capability. Major services provided to SACI investigators by the MS Shared Resource include: molecular mass determination; protein identification from solution or polyacrylamide gel; sequence analysis; elucidation of sites of post-translational modification, focusing on phosphorylation. Detection limits in the sub-picomole range are routinely obtained, making it possible to realistically characterize proteins and peptides isolated from biological samples.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA054174-12
Application #
6689703
Study Section
Subcommittee E - Prevention &Control (NCI)
Project Start
2002-08-26
Project End
2006-07-31
Budget Start
Budget End
Support Year
12
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Ctrc Research Foundation
Department
Type
DUNS #
City
San Antonio
State
TX
Country
United States
Zip Code
78229
Deng, Yilun; Qin, Yuejuan; Srikantan, Subramanya et al. (2018) The TMEM127 human tumor suppressor is a component of the mTORC1 lysosomal nutrient-sensing complex. Hum Mol Genet 27:1794-1808
Wei, Zhen; Panneerdoss, Subbarayalu; Timilsina, Santosh et al. (2018) Topological Characterization of Human and Mouse m5C Epitranscriptome Revealed by Bisulfite Sequencing. Int J Genomics 2018:1351964
Chiang, Huai-Chin; Zhang, Xiaowen; Zhao, Xiayan et al. (2018) Gene-Specific Genetic Complementation between Brca1 and Cobra1 During Mouse Mammary Gland Development. Sci Rep 8:2731
Zanotto-Filho, Alfeu; Rajamanickam, Subapriya; Loranc, Eva et al. (2018) Sorafenib improves alkylating therapy by blocking induced inflammation, invasion and angiogenesis in breast cancer cells. Cancer Lett 425:101-115
Segovia, Jesus A; Chang, Te-Hung; Winter, Vicki T et al. (2018) NLRP3 Is a Critical Regulator of Inflammation and Innate Immune Cell Response during Mycoplasma pneumoniae Infection. Infect Immun 86:
Donegan, Jennifer J; Boley, Angela M; Lodge, Daniel J (2018) Embryonic stem cell transplants as a therapeutic strategy in a rodent model of autism. Neuropsychopharmacology 43:1789-1798
Vaidya, Anand; Flores, Shahida K; Cheng, Zi-Ming et al. (2018) EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease. N Engl J Med 378:1259-1261
Cepeda, Sergio; Cantu, Carolina; Orozco, Stephanie et al. (2018) Age-Associated Decline in Thymic B Cell Expression of Aire and Aire-Dependent Self-Antigens. Cell Rep 22:1276-1287
Snead, Wilton T; Zeno, Wade F; Kago, Grace et al. (2018) BAR scaffolds drive membrane fission by crowding disordered domains. J Cell Biol :
Ramasamy, Kumaraguruparan; Balasubramanian, Sowmya; Manickam, Krishnan et al. (2018) Mycoplasma pneumoniae Community-Acquired Respiratory Distress Syndrome Toxin Uses a Novel KELED Sequence for Retrograde Transport and Subsequent Cytotoxicity. MBio 9:

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