The overarching objective of the Integrated Molecular Technologies (IMT) Core is to promote and facilitate basic and translational Gl research by providing CURE: DDRCC investigators with access to state-of-the-art molecular technologies, including: 1) expertise, equipment and services for systems biology and high-throughput screening analyses; 2) expertise and equipment for peptide synthesis and protein/peptide analysis, and 3) expertise and viral vector cloning and production services to genetically engineer mammalian cell lines and primary cells for expression or inhibition of proteins and miRNAs both in vitro and in vivo. To fulfill this objective, the IMT personnel will pursue the following specific aims: 1) To provide CURE: DDRCC researchers with individually customized services that require highly specialized expertise and/or instrumentation at minimal cost. These services include (but are not limited to): a) providing or facilitating access to specialized protocols and/or expensive instrumentation for profiling changes in gene expression and cellular phenotype, high-throughput molecular screening of drug candidates, and analysis of peptide and protein expression and function; b) design and characterization of custom peptides and isolation and characterization of peptide/protein analysis; c) design, construction, and production of custom gene delivery vectors for expression of a specific peptide or protein of interest. 2) To serve as an educational and advisory resource for CURE: DDRCC researchers who wish to utilize state-of-the-art molecular technologies to further their own research studies. These services include (but are not limited to): a) training, consultation, and troubleshooting in techniques for design, implementation, and bioinformatic analysis of customized genomic and cytologic profiling assays and molecular screening assays; b) training, consultation, and troubleshooting in techniques for design, and use of custom peptides and quantitative analysis of protein expression and function, and c) training, consultation, and troubleshooting in techniques to genetically engineer mammalian cells in vitro and in vivo for functional protein expression or knockdown.

Public Health Relevance

By providing CURE: DDRCC researchers with highly specialized expertise and equipment for analysis and manipulation of gene and protein expression and high-throughput screening of therapeutic compounds, the Integrated Molecular Technologies Core supports our mission to investigate gastrointestinal biology and to develop new therapies for gastrointestinal disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK041301-29
Application #
9392154
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2017-12-01
Budget End
2018-11-30
Support Year
29
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Salehi, Sahar; Sosa, Rebecca A; Jin, Yi-Ping et al. (2018) Outside-in HLA class I signaling regulates ICAM-1 clustering and endothelial cell-monocyte interactions via mTOR in transplant antibody-mediated rejection. Am J Transplant 18:1096-1109
Biczo, Gyorgy; Vegh, Eszter T; Shalbueva, Natalia et al. (2018) Mitochondrial Dysfunction, Through Impaired Autophagy, Leads to Endoplasmic Reticulum Stress, Deregulated Lipid Metabolism, and Pancreatitis in Animal Models. Gastroenterology 154:689-703
Fulcher, Jennifer A; Shoptaw, Steven; Makgoeng, Solomon B et al. (2018) Brief Report: Recent Methamphetamine Use Is Associated With Increased Rectal Mucosal Inflammatory Cytokines, Regardless of HIV-1 Serostatus. J Acquir Immune Defic Syndr 78:119-123
Jin, Yi-Ping; Valenzuela, Nicole M; Zhang, Xiaohai et al. (2018) HLA Class II-Triggered Signaling Cascades Cause Endothelial Cell Proliferation and Migration: Relevance to Antibody-Mediated Transplant Rejection. J Immunol 200:2372-2390
Gupta, Arpana; Mayer, Emeran A; Labus, Jennifer S et al. (2018) Sex Commonalities and Differences in Obesity-Related Alterations in Intrinsic Brain Activity and Connectivity. Obesity (Silver Spring) 26:340-350
Wang, Bo; Rong, Xin; Palladino, Elisa N D et al. (2018) Phospholipid Remodeling and Cholesterol Availability Regulate Intestinal Stemness and Tumorigenesis. Cell Stem Cell 22:206-220.e4
Chen, Wenling; Ennes, Helena S; McRoberts, James A et al. (2018) Mechanisms of ?-opioid receptor inhibition of NMDA receptor-induced substance P release in the rat spinal cord. Neuropharmacology 128:255-268
Strege, Peter R; Mazzone, Amelia; Bernard, Cheryl E et al. (2018) Irritable bowel syndrome patients have SCN5A channelopathies that lead to decreased NaV1.5 current and mechanosensitivity. Am J Physiol Gastrointest Liver Physiol 314:G494-G503
Mazzoni, M; Karunaratne, T B; Sirri, F et al. (2018) Enteroendocrine profile of ?-transducin and ?-gustducin immunoreactive cells in the chicken (Gallus domesticus) gastrointestinal tract. Poult Sci 97:4063-4072
Hilfenhaus, Georg; Nguyen, Dai Phuong; Freshman, Jonathan et al. (2018) Vav3-induced cytoskeletal dynamics contribute to heterotypic properties of endothelial barriers. J Cell Biol 217:2813-2830

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