In this NIH Metabolomics Common Fund center proposal for a Regional Comprehensive Metabolomics Resource Core (RCMRC), """"""""Resource Center for Stable Isotope-Resolved Metabolomics"""""""", we aim to continue and expand on our current, successful Center for Regulatory and Environmental Analytical Metabolomics (CREAM). The role of the Administrative Core is to provide overall administration, budgetary management, oversee analytical services (e.g. sample tracking, analysis status, and billing), and oversight for the other 4 Cores'operations. The Core PI list comprises the current directorship of CREAM, ensuring smooth personnel and management transition to the NIH RCMRC version of CREAM. This section describes both current and expanded operations with regards to administration of the proposed center, and to ensure complete operational and policy harmony with the Common Funds goals. The Administrative Core will be responsible for all aspects of service scheduling and recharges, financial management of the annually awarded Pilot and Feasibility projects, maintaining all budgets and cost reporting of Cores, organizing outreach workshops and symposia, as well as coordinating annual reports, regular meetings among the project personnel and all interaction?s with other RCMRC's, program wide Executive Committee, the Data Repository and Coordinating Center (DRCC), NIH Project Scientist &staff, and any other appropriate entities.
The specific aims of the Administrative Core are as follows: SA1. Establish the RCMRC-CREAM and evolve a tiered set of services for users. SA2. Coordinate with Clients and manage sample, analytical, and data workflow across all Cores. SA3. Provide administrative and budgetary oversight for the RCMRC-CREAM and across all Cores. SA4. Coordinate external efforts with other RCMRC facilities, the Executive Committee, NIH Project Scientists and staff, NIH Common Fund programs, and any other appropriate entities. SA5. Plan and implement transition to self-sustaining operations.
The Administrative Core is necessary to operate this complex metabolomics center for accelerating systems biochemical understanding of human diseases, from which novel biomarkers and therapeutic targets for many critical health issues can be uncovered and translated into clinical development.
|Zaytseva, Yekaterina Y; Rychahou, Piotr G; Le, Anh-Thu et al. (2018) Preclinical evaluation of novel fatty acid synthase inhibitors in primary colorectal cancer cells and a patient-derived xenograft model of colorectal cancer. Oncotarget 9:24787-24800|
|Crooks, Daniel R; Maio, Nunziata; Lane, Andrew N et al. (2018) Acute loss of iron-sulfur clusters results in metabolic reprogramming and generation of lipid droplets in mammalian cells. J Biol Chem 293:8297-8311|
|Lian, Gaojian; Gnanaprakasam, Jn Rashida; Wang, Tingting et al. (2018) Glutathione de novo synthesis but not recycling process coordinates with glutamine catabolism to control redox homeostasis and directs murine T cell differentiation. Elife 7:|
|Sun, Ramon C; Fan, Teresa W-M; Deng, Pan et al. (2017) Noninvasive liquid diet delivery of stable isotopes into mouse models for deep metabolic network tracing. Nat Commun 8:1646|
|Wang, Qingding; Zhou, Yuning; Rychahou, Piotr et al. (2017) Ketogenesis contributes to intestinal cell differentiation. Cell Death Differ 24:458-468|
|Yang, Ye; Fan, Teresa W-M; Lane, Andrew N et al. (2017) Chloroformate derivatization for tracing the fate of Amino acids in cells and tissues by multiple stable isotope resolved metabolomics (mSIRM). Anal Chim Acta 976:63-73|
|Yao, Sen; Flight, Robert M; Rouchka, Eric C et al. (2017) Perspectives and expectations in structural bioinformatics of metalloproteins. Proteins 85:938-944|
|Salem, Shaimaa M; Weidenbach, Stevi; Rohr, Jürgen (2017) Two Cooperative Glycosyltransferases Are Responsible for the Sugar Diversity of Saquayamycins Isolated from Streptomyces sp. KY 40-1. ACS Chem Biol 12:2529-2534|
|Yao, Sen; Flight, Robert M; Rouchka, Eric C et al. (2017) Aberrant coordination geometries discovered in the most abundant metalloproteins. Proteins 85:885-907|
|Matrka, Marie C; Watanabe, Miki; Muraleedharan, Ranjithmenon et al. (2017) Overexpression of the human DEK oncogene reprograms cellular metabolism and promotes glycolysis. PLoS One 12:e0177952|
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