Calcium is the single most important messenger molecule in mammalian cells. Fluctuations in its concentration control a myriad of processes from gene expression to wound healing. The goal of this proposal is the chemical synthesis of photochemically based probes that will be used to control calcium concentration in living animals. New laser and microscope technologies now permit the imaging of structures as small single synapses in vivo. We wish to use this technology (the two-photon microscope) to be more than passive observers of cell function. We propose to make chemical probes that will allow us to actively intervene in the calcium dynamics of individual cells in vivo. To do this we will take advantage of a new chromophore we have recently made (called """"""""NDBF""""""""), that is uniquely sensitive to two-photon excitation. We will develop functionally inert (or """"""""caged"""""""") derivatives of IPS or calcium receptor agonists that are photochemically liberated by two-photon photolysis. These new probes will be used in collaboration with other scientists to study how basic calcium-regulated processes encode memory at the level of single synapses. They will also be used, in concert with two-photon imaging of calcium, to probe the dynamics of calcium signaling in mouse models of disease states such epilepsy and Alzheimer's, as well as during nicotine addiction. Calcium signaling is significantly perturbed by these states. The photochemical probes we propose to develop will enable us to examine these changes in living animals for the first time.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM053395-13
Application #
7628101
Study Section
Neurotransporters, Receptors, and Calcium Signaling Study Section (NTRC)
Program Officer
Shapiro, Bert I
Project Start
1995-02-01
Project End
2011-04-30
Budget Start
2009-05-01
Budget End
2010-04-30
Support Year
13
Fiscal Year
2009
Total Cost
$297,387
Indirect Cost
Name
Drexel University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
002604817
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Passlick, Stefan; Ellis-Davies, Graham C R (2018) Comparative one- and two-photon uncaging of MNI-glutamate and MNI-kainate on hippocampal CA1 neurons. J Neurosci Methods 293:321-328
Passlick, Stefan; Richers, Matthew T; Ellis-Davies, Graham C R (2018) Thermodynamically Stable, Photoreversible Pharmacology in Neurons with One- and Two-Photon Excitation. Angew Chem Int Ed Engl 57:12554-12557
Richers, Matthew T; Tran, Dinh Du; Wachtveitl, Josef et al. (2018) Coumarin-diene photoswitches for rapid and efficient isomerization with visible light. Chem Commun (Camb) 54:4983-4986
Agarwal, Hitesh K; Zhai, Shenyu; Surmeier, D James et al. (2017) Intracellular Uncaging of cGMP with Blue Light. ACS Chem Neurosci 8:2139-2144
Passlick, Stefan; Kramer, Paul F; Richers, Matthew T et al. (2017) Two-color, one-photon uncaging of glutamate and GABA. PLoS One 12:e0187732
Richers, Matthew T; Amatrudo, Joseph M; Olson, Jeremy P et al. (2017) Cloaked Caged Compounds: Chemical Probes for Two-Photon Optoneurobiology. Angew Chem Int Ed Engl 56:193-197
Howarth, Clare; Sutherland, Brad; Choi, Hyun B et al. (2017) A Critical Role for Astrocytes in Hypercapnic Vasodilation in Brain. J Neurosci 37:2403-2414
Agarwal, Hitesh K; Janicek, Radoslav; Chi, San-Hui et al. (2016) Calcium Uncaging with Visible Light. J Am Chem Soc 138:3687-93
Sajo, Mari; Ellis-Davies, Graham; Morishita, Hirofumi (2016) Lynx1 Limits Dendritic Spine Turnover in the Adult Visual Cortex. J Neurosci 36:9472-8
Kantevari, Srinivas; Passlick, Stefan; Kwon, Hyung-Bae et al. (2016) Development of Anionically Decorated Caged Neurotransmitters: In Vitro Comparison of 7-Nitroindolinyl- and 2-(p-Phenyl-o-nitrophenyl)propyl-Based Photochemical Probes. Chembiochem 17:953-61

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