? CHEMICAL LIBRARY SCREENING SHARED RESOURCE The Chemical Library Screening (CLS) Shared Resource is managed by the Cancer Center. This resource offers Center scientists the ability to develop and conduct small- and large-scale chemical library screens and perform hit optimization and validation for generating selective probes/leads modulating biochemical and cellular processes in cancer. In addition, CLS provides faculty with access to technology, expertise, and infrastructure resources to develop novel assays for characterizing cellular targets involved in tumor initiation and pathogenesis and to advance the development of new lead molecules for anti-tumor therapies. CLS consists of four specialized but highly integrated facilities: High-Throughput Assay Development (HT-AD), Compound Management and High-Throughput Screening (CM-HTS), High-Content Screening (HCS), and Medicinal Chemistry and Drug Metabolism/Pharmacokinetics (MedChem/DMPK). The facilities physically reside within the Conrad Prebys Center for Chemical Genomics (Prebys Center) at SBP, which occupies more than 12,000 sq. ft. of laboratory space and houses substantial HTS and HCS assay development and screening instrumentation capabilities. CLS has access to a broad spectrum of diverse and focused small-molecule collections, several integrated liquid handling systems, and a plethora of detection instruments, capable of performing assays in any mode, including live-cell image-based assays requiring temperature and CO2 control. The Prebys Center grew out of the Cancer Center's CLS Shared Resource, which was initiated in the 2003 CCSG renewal. This support has been leveraged with several large grant awards and philanthropic funds. Initially awarded a grant as one of ten NIH Molecular Libraries Screening Network Comprehensive Centers, the Prebys Center was later selected as one of four NIH- designated Molecular Libraries Probe Production Centers Network comprehensive screening centers. It is also one of seven dedicated Centers for the NCI Chemical Biology Consortium (CBC). Despite the growth of the Prebys Center, the CLS Core remains of crucial importance to Center investigators because it provides an important interactive entry point to ensure that they derive the maximum scientific benefit from these world class chemical biology and drug discovery capabilities, enabling both fundamental and translational scientific endeavors. In the past 5 years, the Core has additionally enabled >100 assay development projects for Cancer Center investigators, resulting in >25 full HTS campaigns to support the goal of early translation. It has provided services for 36 Center investigators representing all three programs. The data generated have supported 24 successful grants from 16 Center members and numerous publications, including 20 publications co-authored by CLS staff.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA030199-39
Application #
9934924
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2020-05-27
Budget End
2021-04-30
Support Year
39
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Sanford Burnham Prebys Medical Discovery Institute
Department
Type
DUNS #
020520466
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Lundquist, Mark R; Goncalves, Marcus D; Loughran, Ryan M et al. (2018) Phosphatidylinositol-5-Phosphate 4-Kinases Regulate Cellular Lipid Metabolism By Facilitating Autophagy. Mol Cell 70:531-544.e9
Ramirez, Monica L Gonzalez; Poreba, Marcin; Snipas, Scott J et al. (2018) Extensive peptide and natural protein substrate screens reveal that mouse caspase-11 has much narrower substrate specificity than caspase-1. J Biol Chem 293:7058-7067
Wei, Yang; Toth, Julia I; Blanco, Gabrielle A et al. (2018) Adapted ATPase domain communication overcomes the cytotoxicity of p97 inhibitors. J Biol Chem 293:20169-20180
Tinoco, Roberto; Carrette, Florent; Henriquez, Monique L et al. (2018) Fucosyltransferase Induction during Influenza Virus Infection Is Required for the Generation of Functional Memory CD4+ T Cells. J Immunol 200:2690-2702
Wonder, Emily; Simón-Gracia, Lorena; Scodeller, Pablo et al. (2018) Competition of charge-mediated and specific binding by peptide-tagged cationic liposome-DNA nanoparticles in vitro and in vivo. Biomaterials 166:52-63
Limpert, Allison S; Lambert, Lester J; Bakas, Nicole A et al. (2018) Autophagy in Cancer: Regulation by Small Molecules. Trends Pharmacol Sci 39:1021-1032
Fujita, Yu; Khateb, Ali; Li, Yan et al. (2018) Regulation of S100A8 Stability by RNF5 in Intestinal Epithelial Cells Determines Intestinal Inflammation and Severity of Colitis. Cell Rep 24:3296-3311.e6
Scully, Kathleen M; Lahmy, Reyhaneh; Signaevskaia, Lia et al. (2018) E47 Governs the MYC-CDKN1B/p27KIP1-RB Network to Growth Arrest PDA Cells Independent of CDKN2A/p16INK4A and Wild-Type p53. Cell Mol Gastroenterol Hepatol 6:181-198
Borlido, Joana; Sakuma, Stephen; Raices, Marcela et al. (2018) Nuclear pore complex-mediated modulation of TCR signaling is required for naïve CD4+ T cell homeostasis. Nat Immunol 19:594-605
Follis, Ariele Viacava; Llambi, Fabien; Kalkavan, Halime et al. (2018) Regulation of apoptosis by an intrinsically disordered region of Bcl-xL. Nat Chem Biol 14:458-465

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