This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. This subproject involves the development and construction of an ESR microscope operating at pulsed mode. The ESR microscope is conceptually similar to the well known Magnetic Resonance Imaging (MRI) system. The main differences are with the type of spins used for the measurements (electron vs. protons in MRI), and the image resolution (microns vs. mm). Consequently, most biologically-related samples must be doped or labelled with stable radicals to facilitate the ESR measurement (similar to dyes in optical microscopy). Furthermore, the samples must be with a typical size of no more than 1-2 mm. When combined with optical microscopy, the pulsed ESR microscope can be a valuable tool in bio-science. Spatially resolved parameters such as diffusion tensor, O2 concentration, relaxation times (T1, T2), and the ESR lineshape can reveal a wealth of information in model and live systems, inaccessible by optical methods. In the past attempts has been made to combine NMR and optical microscopy, but with limited success due to the limited resolution of NMR (~10 microns) and its high cost. The ESR microscope, which is much more sensitive, should achieve magnetic resonance images with resolution comparable to optical method (~ 1 micron), and at much lower cost (simple electromagnet vs. large superconducting magnetic in NMR microscopy).We have constructed an initial prototype of the pulsed ESR microscope. The system is made of a home-built 6-17 GHz pulsed microwave bridge, a pulsed gradient driver, a computer for system control and data acquisition, and a pulsed imaging probe (resonator+ gradient coils). Three dimensional ESR images with a resolution of 3x3x8 microns were demonstrated at 16 GHz. Further progress to higher frequencies 9up to ~60 GHz, would facilitate the required sub-micron image resolution.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
2P41RR016292-06
Application #
7420481
Study Section
Special Emphasis Panel (ZRG1-BCMB-K (40))
Project Start
2006-09-15
Project End
2007-08-31
Budget Start
2006-09-15
Budget End
2007-08-31
Support Year
6
Fiscal Year
2006
Total Cost
$34,866
Indirect Cost
Name
Cornell University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
872612445
City
Ithaca
State
NY
Country
United States
Zip Code
14850
Jain, Rinku; Vanamee, Eva S; Dzikovski, Boris G et al. (2014) An iron-sulfur cluster in the polymerase domain of yeast DNA polymerase ?. J Mol Biol 426:301-8
Pratt, Ashley J; Shin, David S; Merz, Gregory E et al. (2014) Aggregation propensities of superoxide dismutase G93 hotspot mutants mirror ALS clinical phenotypes. Proc Natl Acad Sci U S A 111:E4568-76
Georgieva, Elka R; Borbat, Peter P; Ginter, Christopher et al. (2013) Conformational ensemble of the sodium-coupled aspartate transporter. Nat Struct Mol Biol 20:215-21
Airola, Michael V; Sukomon, Nattakan; Samanta, Dipanjan et al. (2013) HAMP domain conformers that propagate opposite signals in bacterial chemoreceptors. PLoS Biol 11:e1001479
Airola, Michael V; Huh, Doowon; Sukomon, Nattakan et al. (2013) Architecture of the soluble receptor Aer2 indicates an in-line mechanism for PAS and HAMP domain signaling. J Mol Biol 425:886-901
Sun, Yan; Zhang, Ziwei; Grigoryants, Vladimir M et al. (2012) The internal dynamics of mini c TAR DNA probed by electron paramagnetic resonance of nitroxide spin-labels at the lower stem, the loop, and the bulge. Biochemistry 51:8530-41
Smith, Andrew K; Freed, Jack H (2012) Dynamics and ordering of lipid spin-labels along the coexistence curve of two membrane phases: an ESR study. Chem Phys Lipids 165:348-61
Yu, Renyuan Pony; Darmon, Jonathan M; Hoyt, Jordan M et al. (2012) High-Activity Iron Catalysts for the Hydrogenation of Hindered, Unfunctionalized Alkenes. ACS Catal 2:1760-1764
Gaffney, Betty J; Bradshaw, Miles D; Frausto, Stephen D et al. (2012) Locating a lipid at the portal to the lipoxygenase active site. Biophys J 103:2134-44
Dzikovski, Boris; Tipikin, Dmitriy; Freed, Jack (2012) Conformational distributions and hydrogen bonding in gel and frozen lipid bilayers: a high frequency spin-label ESR study. J Phys Chem B 116:6694-706

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