The Proteomics Shared Resource provides AECC researchers with comprehensive mass spectrometry technologies for analysis of proteins, peptides, carbohydrates, lipids and. unknowns. Staff scientists plan and execute proteomics-based analyses, carry out intensive data analysis, and interact closely with AECC scientists on all aspects of their experiments. Services include: MALDI-TOF, ESI- and FT-ICR mass spectrometry;bioinformatics searches and customized data analysis;2D-gels, 2D-DIGE and high-resolution HPLC;rapid turnaround time for protein ID from gel bands, immunoaffinity isolations or specialty preparations;identification of components of protein complexes;post-translational modifications of proteins;protocols and training in methods and data acquisition;quantitative proteomics using SILAC, SILAM, ^?0, iTRAQ and label-free methods;protein dynamics and biomolecular interactions using hydrogen/deuterium exchange-mass spectrometry;confirmation of synthetic and recombinant molecules;and high-resolution analysis by FT-ICR-MS of metabolites, drugs, peptides and small molecules. Quantitative mass spectrometry experiments have assumed new importance in the past project period, and are anticipated to continue to increase. New services include: (i) imaging mass spectrometry, whereby frozen tissue sections can be analyzed for small proteins or small molecules, transmitters or metabolites and (ii) triple quadrupole mass spectrometry for the quantitative analysis of drugs and their metabolites in biological fluids. The science of the AECC members helps to drive the technology offered in the facility. For example, the demand for imaging mass spectrometry led to the successful shared instrumentation grant application that awarded funds for its implementation. Studies of protein dynamics involve close interactions with several AECC faculty and have been helpful in designing new drug candidates. Analysis of kinetic isotope effects (KIE) is utilized in the design of transition- state inhibitors. The Proteomics Shared Resource provides training on the analytical tools available to users such as the MASCOT search engine and associated modules. Protein Scaffold, ProteolQ, MSnbase to integrate quantitative proteomics with statistical analysis, and specialized software for Selected Reaction Monitoring. A Proteomics course is offered which provides instruction in advanced data analysis.

Public Health Relevance

The Proteomics Shared Resource provides comprehensive mass spectrometry technologies for analysis of proteins, peptides, carbohydrates, lipids and unknowns that support the translational research mission and goals of the Albert Einstein Cancer Center (AECC). As an NCI-designated Cancer Center, AECC contributes to the national effort to reduce morbidity and mortality from cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-41
Application #
8753315
Study Section
Subcommittee B - Comprehensiveness (NCI)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
41
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
City
Bronx
State
NY
Country
United States
Zip Code
10461
Sharma, Yogeshwar; Liu, Jinghua; Kristian, Kathleen E et al. (2018) In Atp7b-/- Mice Modeling Wilson's Disease Liver Repopulation with Bone Marrowderived Myofibroblasts or Inflammatory Cells and not Hepatocytes is Deleterious. Gene Expr :
Iqbal, Niloy Jafar; Lu, Zhonglei; Liu, Shun Mei et al. (2018) Cyclin-dependent kinase 4 is a preclinical target for diet-induced obesity. JCI Insight 3:
Norwood Toro, Laura E; Wang, Yarong; Condeelis, John S et al. (2018) Myosin-IIA heavy chain phosphorylation on S1943 regulates tumor metastasis. Exp Cell Res 370:273-282
De Martino, Daniela; Yilmaz, Emrullah; Orlacchio, Arturo et al. (2018) PI3K blockage synergizes with PLK1 inhibition preventing endoreduplication and enhancing apoptosis in anaplastic thyroid cancer. Cancer Lett 439:56-65
Bhargava, Ragini; Sandhu, Manbir; Muk, Sanychen et al. (2018) C-NHEJ without indels is robust and requires synergistic function of distinct XLF domains. Nat Commun 9:2484
Agalliu, Ilir; Chen, Zigui; Wang, Tao et al. (2018) Oral Alpha, Beta, and Gamma HPV Types and Risk of Incident Esophageal Cancer. Cancer Epidemiol Biomarkers Prev 27:1168-1175
Doyle, Christopher R; Moon, Jee-Young; Daily, Johanna P et al. (2018) A Capsular Polysaccharide-Specific Antibody Alters Streptococcus pneumoniae Gene Expression during Nasopharyngeal Colonization of Mice. Infect Immun 86:
Collu, Giovanna M; Jenny, Andreas; Gaengel, Konstantin et al. (2018) Prickle is phosphorylated by Nemo and targeted for degradation to maintain Prickle/Spiny-legs isoform balance during planar cell polarity establishment. PLoS Genet 14:e1007391
Stepankova, Martina; Bartonkova, Iveta; Jiskrova, Eva et al. (2018) Methylindoles and Methoxyindoles are Agonists and Antagonists of Human Aryl Hydrocarbon Receptor. Mol Pharmacol 93:631-644
Anayannis, Nicole V; Schlecht, Nicolas F; Ben-Dayan, Miriam et al. (2018) Association of an intact E2 gene with higher HPV viral load, higher viral oncogene expression, and improved clinical outcome in HPV16 positive head and neck squamous cell carcinoma. PLoS One 13:e0191581

Showing the most recent 10 out of 1508 publications