? PROTEOMICS SHARED RESOURCE FACILITY The mission of the Proteomics Shared Resource Facility is to provide cost-effective, state-of the-art instrumentation and analytical proteomics expertise to investigators in the Lurie Cancer Center (LCC). The Proteomics Core provides a full array of services including study design, sample preparation, data generation and analysis and interpretation of results. The Core supports work involving the following types of methodologies: 1) protein identification from gels and BioID samples. 2) Quantitative proteomics ? labeled and label-free. 3) Top-down proteomics - qualitative and quantitative, 4) Site-specific PTM analyses, including phosphorylation, acetylation, methylation, glycosylation, palmitoylation, and ubiquitination; 5) Targeted proteomics using selective reaction monitoring (SRM) and related methods; 6) Histone Modification Panel analysis, covering all major histone marks, and 7) Advanced proteomics sample preparation from body fluids (blood, urine, saliva, CSF), tissue, secretome, exosome, and mitochondria. In addition, the Proteomics Core staff provides education and training in sample preparation, instrumental analysis and data analysis to LCC investigators and their laboratory personnel. The Core operates eight liquid chromatography-mass spectrometry systems and since its inception as a former developing core at the time of the last CCSG review, has served over 90 LCC investigators, resulting in over 60 research publications. The Proteomics Core is located on both campuses of Northwestern University (NU). Neil Kelleher, PhD, directs the Facility and works closely with Young Ah Goo, PhD, the Operations Director of the Facility. As a cross- university, cross-campus resource, access to service is available to all Northwestern University investigators, with priority given to LCC researchers. During the next funding period, the Proteomics Core will continue to work closely with LCC researchers to ensure that efficient access and technological expertise in proteomics is available to all research teams engaged in basic, clinical and translational cancer studies.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA060553-26
Application #
9982868
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
26
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Type
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Blair, Kris M; Mears, Kevin S; Taylor, Jennifer A et al. (2018) The Helicobacter pylori cell shape promoting protein Csd5 interacts with the cell wall, MurF, and the bacterial cytoskeleton. Mol Microbiol 110:114-127
Stack, Trevor; Vahabikashi, Amir; Johnson, Mark et al. (2018) Modulation of Schlemm's canal endothelial cell stiffness via latrunculin loaded block copolymer micelles. J Biomed Mater Res A 106:1771-1779
Welch, Whitney A; Spring, Bonnie; Phillips, Siobhan M et al. (2018) Moderating Effects of Weather-Related Factors on a Physical Activity Intervention. Am J Prev Med 54:e83-e89
Karabin, Nicholas B; Allen, Sean; Kwon, Ha-Kyung et al. (2018) Sustained micellar delivery via inducible transitions in nanostructure morphology. Nat Commun 9:624
Kenig-Kozlovsky, Yael; Scott, Rizaldy P; Onay, Tuncer et al. (2018) Ascending Vasa Recta Are Angiopoietin/Tie2-Dependent Lymphatic-Like Vessels. J Am Soc Nephrol 29:1097-1107
Kaplan, Nihal; Ventrella, Rosa; Peng, Han et al. (2018) EphA2/Ephrin-A1 Mediate Corneal Epithelial Cell Compartmentalization via ADAM10 Regulation of EGFR Signaling. Invest Ophthalmol Vis Sci 59:393-406
Ting, See-Yeun; Bosch, Dustin E; Mangiameli, Sarah M et al. (2018) Bifunctional Immunity Proteins Protect Bacteria against FtsZ-Targeting ADP-Ribosylating Toxins. Cell 175:1380-1392.e14
Zhang, Angelica; Veesenmeyer, Jeffrey L; Hauser, Alan R (2018) Phosphatidylinositol 4,5-Bisphosphate-Dependent Oligomerization of the Pseudomonas aeruginosa Cytotoxin ExoU. Infect Immun 86:
Kang, Hong-Jun; Song, Ha Yong; Ahmed, Mohamed A et al. (2018) NQO1 regulates mitotic progression and response to mitotic stress through modulating SIRT2 activity. Free Radic Biol Med 126:358-371
Nahum-Shani, Inbal; Smith, Shawna N; Spring, Bonnie J et al. (2018) Just-in-Time Adaptive Interventions (JITAIs) in Mobile Health: Key Components and Design Principles for Ongoing Health Behavior Support. Ann Behav Med 52:446-462

Showing the most recent 10 out of 1972 publications