application) The main objectives of this core are to provide a number of specialized peptides and molecular probes in a cost-effective manner. Many studies performed at CURE utilize peptide reagents. core investigators are trained in how to make, store, dilute and evaluate peptides properly under experimental conditions. The core helps in characterization of natural or synthetic peptides by amino acid analysis, high performance capillary electrophoresis, high performance liquid chromatography (HPLC), mass spectral analysis and microsequence analysis. The core also provides training, reagents and equipment facilities for the radioimmunoassay as well. Investigators are also provided standard or heavily used peptides either in their native form or modified to impart features such as fluorescence or labeling sites. Molecular probes such as oligodeoxyribonucleotides or cDNA probes are provided and analyzed for appropriate quality to ensure that the acquired or custom made probes are of the highest quality. The core is housed in three different laboratories: The Peptide Biochemistry Laboratory (VA); The Nucleic Acid Probes Laboratory (VA) and the Peptide Synthesis and Purification Laboratory (UCLA). The core laboratories are well equipped with all the basic equipment, such as HPLC, dual wavelength UV detector, variable wavelength UV detector, gamma counter, a variety of HPLC columns and centrifuges. Other specialized techniques, such as microsequence, NMR, circular dichroism, mass spectrometry measurements, are performed at various other UCLA laboratories coordinated by the core. The core facilities are currently being utilized by 25 CURE investigators in their projects, and the utilization had resulted in 87 publications during the previous funding period.

Project Start
2000-06-01
Project End
2000-11-30
Budget Start
Budget End
Support Year
11
Fiscal Year
2000
Total Cost
$293,330
Indirect Cost
Name
University of California Los Angeles
Department
Type
DUNS #
119132785
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Chen, Wenling; Taché, Yvette; Marvizón, Juan Carlos (2018) Corticotropin-Releasing Factor in the Brain and Blocking Spinal Descending Signals Induce Hyperalgesia in the Latent Sensitization Model of Chronic Pain. Neuroscience 381:149-158
Gupta, Arpana; Woodworth, Davis C; Ellingson, Benjamin M et al. (2018) Disease-Related Microstructural Differences in the Brain in Women With Provoked Vestibulodynia. J Pain 19:528.e1-528.e15
Ziyad, Safiyyah; Riordan, Jesse D; Cavanaugh, Ann M et al. (2018) A Forward Genetic Screen Targeting the Endothelium Reveals a Regulatory Role for the Lipid Kinase Pi4ka in Myelo- and Erythropoiesis. Cell Rep 22:1211-1224
Marcus, Elizabeth A; Sachs, George; Scott, David R (2018) Acid-regulated gene expression of Helicobacter pylori: Insight into acid protection and gastric colonization. Helicobacter 23:e12490
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

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