The Koch Institute High Throughput Sciences Core (HTS Core) provides automated technologies, expertise and training that allows Cancer Center Members to investigate the interplay between biomaterials, biomolecules, small molecules and cells in a high-throughput, multiplexed manner to enable drug and gene discovery, drug delivery, toxicology, and systems biology applications. The HTS Core possesses state-of-the-art robotic instrumentation, an array of biological tools, including validated cell lines and curated libraries, and an exceptional staff with expertise in assay development and adaptation, screening execution, and robotics workflows. HTS Core activities were established in 2011, with support from CCSG Developmental Funds and Institutional support. In the prior submission, HTS activities were embedded in the Koch Institute Genomics Core, reflecting their extensive interactions. During this current period, the HTS Core has greatly expanded its roles and impact for both Center Members and other Koch Institute Cores. Given this, and on the advice of our SAB, we are requesting funding for High Throughput Sciences as a stand-alone Core. In the current funding period, the HTS Core added a significant number of new capabilities and modified existing services, including: a new high throughput flow cytometer and tissue processing equipment; added >55,000 new compounds to small molecule libraries; automated workflows for ELISAs, high content imaging and HT sample preparation pipelines, including automated plate-based HT ChIP-Seq sample preparation (collaborating with the Integrated Genomics & Bioinformatics Core); and cell line management services, including mycoplasma testing and banking of mycoplasma-free cell lines. Center Member Core use has been strong: 66% of Center Members use the Core, account for 73% of Core service use, and include investigators from all three Research Programs. In the upcoming period, the HTS Core will continue to offer a wide range of state-of-the-art services to support Center Member research programs, and will evaluate emerging capabilities in the context of Center Member needs and interests. A number of new initiatives are planned, including: acquisition and evaluation of new equipment; upgrades to existing equipment; acquisition of new CRISPR and targeted small molecule libraries; establishment of small molecule screening in zebrafish; continued collaboration with other Koch Institute Core Facilities to develop technology and streamline workflows; deployment of a custom-built LIMS system to manage library materials and screening assay data; dataset sharing to support development of machine learning algorithms; and collaborating with other Koch Institute Cores to develop a monthly workshop series to support Center Members? access to imaging technology platforms and data analysis. This Shared Resource is essential to the success of the Koch Institute mission and provides exceptional value to the CCSG. The requested CCSG budget for Year 49 is increased by 1.6% over the Core CCSG budget for the current period (Year 48).

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA014051-49
Application #
9937092
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
49
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Type
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02142
Tentori, Augusto M; Nagarajan, Maxwell B; Kim, Jae Jung et al. (2018) Quantitative and multiplex microRNA assays from unprocessed cells in isolated nanoliter well arrays. Lab Chip 18:2410-2424
Parisi, Tiziana; Balsamo, Michele; Gertler, Frank et al. (2018) The Rb tumor suppressor regulates epithelial cell migration and polarity. Mol Carcinog 57:1640-1650
Gam, Jeremy J; Babb, Jonathan; Weiss, Ron (2018) A mixed antagonistic/synergistic miRNA repression model enables accurate predictions of multi-input miRNA sensor activity. Nat Commun 9:2430
Chen, Huihui; Cho, Kin-Sang; Vu, T H Khanh et al. (2018) Commensal microflora-induced T cell responses mediate progressive neurodegeneration in glaucoma. Nat Commun 9:3209
Tam, Brooke E; Hao, Yining; Sikes, Hadley D (2018) An examination of critical parameters in hybridization-based epigenotyping using magnetic microparticles. Biotechnol Prog 34:1589-1595
Ramadi, Khalil B; Dagdeviren, Canan; Spencer, Kevin C et al. (2018) Focal, remote-controlled, chronic chemical modulation of brain microstructures. Proc Natl Acad Sci U S A 115:7254-7259
Knouse, Kristin A; Lopez, Kristina E; Bachofner, Marc et al. (2018) Chromosome Segregation Fidelity in Epithelia Requires Tissue Architecture. Cell 175:200-211.e13
Sabari, Benjamin R; Dall'Agnese, Alessandra; Boija, Ann et al. (2018) Coactivator condensation at super-enhancers links phase separation and gene control. Science 361:
Clancy-Thompson, Eleanor; Devlin, Christine A; Tyler, Paul M et al. (2018) Altered Binding of Tumor Antigenic Peptides to MHC Class I Affects CD8+ T Cell-Effector Responses. Cancer Immunol Res 6:1524-1536
Fiedler, Eleanor R C; Bhutkar, Arjun; Lawler, Emily et al. (2018) In vivo RNAi screening identifies Pafah1b3 as a target for combination therapy with TKIs in BCR-ABL1 + BCP-ALL. Blood Adv 2:1229-1242

Showing the most recent 10 out of 904 publications