The Mass Spectrometry Shared Resource is a specialized facility with the primary goal of protein identification, characterization and quantitation. CSHL has had a peptide sequencing and proteomics facility for over two decades, but the facility was extensively re-equipped in 2008 following the recommendations of the External Advisory Committee, and was housed within the Keck Structural Biology laboratory on the ground floor of the Beckman building. The Resource provides Cancer Center members with access to up-to-date mass spectrometry instrumentation and specialized technical expertise. Services used by the majority of Cancer Center members include protein and protein complex identification, characterization of protein post translational modifications, quantitative peptide MRM assays and quantitative whole-proteome screens using 2D LCMS with iTRAQ or SILAC. More specialized services have undertaken quantitative phosphoproteomic and cysteine proteomics screens, lipid and carbohydrate analyses, metabolomics profiling and specific MRM assays of drugs and other small molecule metabolites. The Shared Resource performs all the data analysis for the quantitative screens and has developed new tools for the merging of large datasets across multiple, independent experiments. All of these services are highly technical and labor intensive. Without the Mass Spectrometry Shared Resource it would be extremely difficult for individual investigators to have access to this type of instrumentation and analyses and these types of services, which are often critical to their research programs. Over the last funding period the Resource has updated HPLC equipment to allow for high-resolution ultra-high pressure liquid chromatography (UHPLC) and built a dedicated 64-processor cluster for database searching. In summary, the Shared Resource provides the user group with state-of-the-art instrumentation and advanced technical support to help accelerate cancer research at CSHL. Over the past five years, the Mass Spectrometry Shared Resource was utilized by 16 Cancer Center members (43% of members), accounting for a majority of its use. This Resource contributed to 29 publications by Cancer Center members over this time period.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA045508-29
Application #
9151082
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2016-08-01
Budget End
2017-07-31
Support Year
29
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Krishnan, Navasona; Bonham, Christopher A; Rus, Ioana A et al. (2018) Harnessing insulin- and leptin-induced oxidation of PTP1B for therapeutic development. Nat Commun 9:283
Pommier, Arnaud; Anaparthy, Naishitha; Memos, Nicoletta et al. (2018) Unresolved endoplasmic reticulum stress engenders immune-resistant, latent pancreatic cancer metastases. Science 360:
Krishnan, Navasona; Felice, Christy; Rivera, Keith et al. (2018) DPM-1001 decreased copper levels and ameliorated deficits in a mouse model of Wilson's disease. Genes Dev 32:944-952
Tiriac, Herve; Bucobo, Juan Carlos; Tzimas, Demetrios et al. (2018) Successful creation of pancreatic cancer organoids by means of EUS-guided fine-needle biopsy sampling for personalized cancer treatment. Gastrointest Endosc 87:1474-1480
Nattestad, Maria; Goodwin, Sara; Ng, Karen et al. (2018) Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. Genome Res 28:1126-1135
Connell, Claire M; Raby, Sophie E M; Beh, Ian et al. (2018) Cancer Immunotherapy Trials Underutilize Immune Response Monitoring. Oncologist 23:116-117
Wong, Mandy S; Kinney, Justin B; Krainer, Adrian R (2018) Quantitative Activity Profile and Context Dependence of All Human 5' Splice Sites. Mol Cell 71:1012-1026.e3
Snider, Justin M; Snider, Ashley J; Obeid, Lina M et al. (2018) Probing de novo sphingolipid metabolism in mammalian cells utilizing mass spectrometry. J Lipid Res 59:1046-1057
Stacchiotti, Silvia; Mir, Olivier; Le Cesne, Axel et al. (2018) Activity of Pazopanib and Trabectedin in Advanced Alveolar Soft Part Sarcoma. Oncologist 23:62-70
Banito, Ana; Li, Xiang; Laporte, Aimée N et al. (2018) The SS18-SSX Oncoprotein Hijacks KDM2B-PRC1.1 to Drive Synovial Sarcoma. Cancer Cell 33:527-541.e8

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