The Purdue Flow Cytometry Shared Resource (FC-SR) provides advanced cell and particle analysis, cell sorting and single cell genomic capabilities to members of the Purdue University Center for Cancer Research (PCCR). The FC-SR has made major improvements to the facility in terms of equipment, expert personnel and data analysis software. This has allowed the Shared Resource to expand its efforts to provide more cancer researchers with economical and effective access to- and training in- the highly specialized and increasingly sophisticated technologies driving modern advances in cancer diagnostics and therapeutics. Flow cytometry is an analytical tool that uses optical measures to allow users to identify and quantitate cellular features, organelles or structural components. When combined with sorting capabilities, users can identify and isolate single cells that have specific properties or express specific molecules, which can then be further examined and characterized. In cancer research, where the identification and characterization of unique, specific cells with cancer-like characteristics is critical, flow cytometry and cell sorting are vital tools for today's cancer researcher. Purdue's FC-SR provides a broad range of services that supported 40 PCCR investigators' research projects and trained 113 PCCR students and postdoctoral fellows between July 2015 and January 2018. The FC-SR, located in the Bindley Bioscience Center (BBC) of Discovery Park, has continued to expand its technical expertise and instrument capabilities. In 2015, with support from an NIH S10 Shared Instrument Grant, the FC-SR obtained a 5-laser, 18-color BD LSR Fortessa flow cytometer designed to complement the workhorse 5-laser BD FACS Aria Cell Sorter. The growing number of new cancer research faculty at Purdue created an increased demand for live cell sorting of mouse and human cells in biosafety level 2 (BSL-2) conditions. To meet this need, in 2018, the PCCR contributed to the purchase of two additional state-of-the-art cell sorters: a 5-laser BD FACS Aria Fusion and a 4-laser, high-speed BC MoFlo Astrios. The PCCR was also instrumental in the development of the FC-SR's single-cell, genome and transcriptome capabilities, through the acquisition of a Fluidigm C1 system and a 10x Chromium system. The data analysis capabilities of the facility have also continued to grow, with the addition of FCS Express and FlowJo site licenses. Perhaps the most important resource provided by the FC-SR is the expertise that the staff shares. Many of the FC-SR's clients have little, if any, experience conducting cytometry analysis or designing cell sorting or single-cell genomics experiments. In the absence of the FC-SR and its experienced staff, these investigators would have tremendous difficulty in generating cytometry data necessary for competitive external funding.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA023168-40
Application #
10024910
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-08-01
Budget End
2021-06-30
Support Year
40
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Purdue University
Department
Type
DUNS #
072051394
City
West Lafayette
State
IN
Country
United States
Zip Code
47907
Huang, Xinxin; Guo, Bin; Liu, Sheng et al. (2018) Neutralizing negative epigenetic regulation by HDAC5 enhances human haematopoietic stem cell homing and engraftment. Nat Commun 9:2741
Chambers, Andrea M; Lupo, Kyle B; Matosevic, Sandro (2018) Tumor Microenvironment-Induced Immunometabolic Reprogramming of Natural Killer Cells. Front Immunol 9:2517
Shinde, Aparna; Wilmanski, Tomasz; Chen, Hao et al. (2018) Pyruvate carboxylase supports the pulmonary tropism of metastatic breast cancer. Breast Cancer Res 20:76
Nenortas, Nathaniel P; Cinelli, Maris A; Morrell, Andrew E et al. (2018) Activity of Aromathecins against African Trypanosomes. Antimicrob Agents Chemother 62:
Norvil, Allison B; Petell, Christopher J; Alabdi, Lama et al. (2018) Dnmt3b Methylates DNA by a Noncooperative Mechanism, and Its Activity Is Unaffected by Manipulations at the Predicted Dimer Interface. Biochemistry 57:4312-4324
Chambers, Andrea M; Wang, Jiao; Lupo, Kyle B et al. (2018) Adenosinergic Signaling Alters Natural Killer Cell Functional Responses. Front Immunol 9:2533
Serratore, Nina D; Baker, Kortany M; Macadlo, Lauren A et al. (2018) A Novel Sterol-Signaling Pathway Governs Azole Antifungal Drug Resistance and Hypoxic Gene Repression in Saccharomyces cerevisiae. Genetics 208:1037-1055
Wu, Heng; Post, Carol Beth (2018) Protein Conformational Transitions from All-Atom Adaptively Biased Path Optimization. J Chem Theory Comput 14:5372-5382
Denton, Kyle E; Wang, Sijie; Gignac, Michael C et al. (2018) Robustness of In Vitro Selection Assays of DNA-Encoded Peptidomimetic Ligands to CBX7 and CBX8. SLAS Discov 23:417-428
Liu, Wenting; Zhong, Yi-Fang; Liu, Liu-Yi et al. (2018) Solution structures of multiple G-quadruplex complexes induced by a platinum(II)-based tripod reveal dynamic binding. Nat Commun 9:3496

Showing the most recent 10 out of 436 publications