1. Overall Objectives The goal of the Imaging Core is to assist PPG investigators in the use of novel molecular probes, labeling, microscopy, and image analysis crucial to achieving the aims of the efforts headed by Drs. Taylor, Newton, Scott, King, and Murphy through the use of advanced imaging approaches. These approaches require state-of-the-art instruments, are constantly evolving, and are practiced by highly specialized personnel with years of training. Because of this, it is cost-effective to have a centralized facility. An economy of effort is achieved by sharing the costs for development and knowledge gained across the 5 groups that will use the same or similar probes and/or technologies. 2. Summary of Services The Imaging Core will: provide training and assistance with confocal and multiphoton immunofluorescence experiments including the use of state-of-the-art reporter technologies such as the tetracysteine-based FIAsH and ReAsH labeling systems, kinase reporters for FRET, and quantum dots enable live-cell imaging and large-area mapping of cells and tissues using advanced light-microscopy instruments provide training and analysis for correlated light and electron microscopic immunolocalization studies including the use of quantum dots, tetracysteine-based photooxidation, and cryosectioning techniques for mitochondria, mitochondrial subfractions, cells, and tissues. provide training and enable supramolecular and molecular characterizations by electron microscopy including electron microscope tomography and high-pressure freezing/freeze substitution and cryoelectron microscopy. provide training and access to software programs for 2- and 3-dimensional biological image analysis.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Program Projects (P01)
Project #
5P01DK054441-13
Application #
8293376
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
2013-03-31
Budget Start
2011-07-01
Budget End
2013-06-30
Support Year
13
Fiscal Year
2011
Total Cost
$115,260
Indirect Cost
Name
University of California San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Flippo, Kyle H; Gnanasekaran, Aswini; Perkins, Guy A et al. (2018) AKAP1 Protects from Cerebral Ischemic Stroke by Inhibiting Drp1-Dependent Mitochondrial Fission. J Neurosci 38:8233-8242
Sengupta, Soham; Nechushtai, Rachel; Jennings, Patricia A et al. (2018) Phylogenetic analysis of the CDGSH iron-sulfur binding domain reveals its ancient origin. Sci Rep 8:4840
Haushalter, Kristofer J; Casteel, Darren E; Raffeiner, Andrea et al. (2018) Phosphorylation of protein kinase A (PKA) regulatory subunit RI? by protein kinase G (PKG) primes PKA for catalytic activity in cells. J Biol Chem 293:4411-4421
Sastri, Mira; Darshi, Manjula; Mackey, Mason et al. (2017) Sub-mitochondrial localization of the genetic-tagged mitochondrial intermembrane space-bridging components Mic19, Mic60 and Sam50. J Cell Sci 130:3248-3260
Smith, F Donelson; Esseltine, Jessica L; Nygren, Patrick J et al. (2017) Local protein kinase A action proceeds through intact holoenzymes. Science 356:1288-1293
Parker, Seth J; Svensson, Robert U; Divakaruni, Ajit S et al. (2017) LKB1 promotes metabolic flexibility in response to energy stress. Metab Eng 43:208-217
Nystoriak, Matthew A; Nieves-CintrĂ³n, Madeline; Patriarchi, Tommaso et al. (2017) Ser1928 phosphorylation by PKA stimulates the L-type Ca2+ channel CaV1.2 and vasoconstriction during acute hyperglycemia and diabetes. Sci Signal 10:
Ilouz, Ronit; Lev-Ram, Varda; Bushong, Eric A et al. (2017) Isoform-specific subcellular localization and function of protein kinase A identified by mosaic imaging of mouse brain. Elife 6:
Nygren, Patrick J; Mehta, Sohum; Schweppe, Devin K et al. (2017) Intrinsic disorder within AKAP79 fine-tunes anchored phosphatase activity toward substrates and drug sensitivity. Elife 6:
Aggarwal-Howarth, Stacey; Scott, John D (2017) Pseudoscaffolds and anchoring proteins: the difference is in the details. Biochem Soc Trans 45:371-379

Showing the most recent 10 out of 216 publications