The Washington University High Resolution NMR Facility, which serves 30 separate chemical, biochemical and biomedical research groups, requests funding to upgrade a poorly functioning 12 year old 600 MHz NMR spectrometer by purchase of a new state-of-the-art console and triple resonance probe. Our current 600 MHz NMR spectrometer was the second 14.4 T system produced by Varian. It has served well a great many research groups throughout the Washington University chemical and biomedical research community during the past 12 years. However, the spectrometer is fully three design-generations behind the current state-of-the-art. Not unexpectedly, inherent design limitations and rapidly advancing technology in the NMR field have long since overtaken the capabilities of this spectrometer. The spectrometer must be updated if the Facility is to provide for the types of modern-day NMR experiments required by our user base. This urgent request is justified by a growing number of deficiencies of our current 600 MHz NMR system. Among these are the following: a) radio-frequency instability leading to inadequate water suppression and diminished performance in multidimensional experiments, b) inability or extreme difficulty to implement routine software revisions or hardware improvements, c) lack of a fourth rf channel for deuterium irradiation experiments with large biomolecules, a cornerstone of modern NMR structural analysis; d) extensive down time due to ever increasing instrument repair, e) signal- to-noise in triple resonance experiments that is down by 60% compared to that offered by current probe technology.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biomedical Research Support Shared Instrumentation Grants (S10)
Project #
1S10RR015715-01
Application #
6288100
Study Section
Special Emphasis Panel (ZRG1-PB (01))
Program Officer
Tingle, Marjorie
Project Start
2001-04-01
Project End
2002-03-31
Budget Start
2001-04-01
Budget End
2002-03-31
Support Year
1
Fiscal Year
2001
Total Cost
$488,045
Indirect Cost
Name
Washington University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Wang, Rongsheng E; Pandita, Raj K; Cai, Jianfeng et al. (2012) Inhibition of heat shock transcription factor binding by a linear polyamide binding in an unusual 1:1 mode. Chembiochem 13:97-104
Wang, Rongsheng E; Hunt, Clayton R; Chen, Jiawei et al. (2011) Biotinylated quercetin as an intrinsic photoaffinity proteomics probe for the identification of quercetin target proteins. Bioorg Med Chem 19:4710-20
Ackerman, Joseph J H; Neil, Jeffrey J (2010) The use of MR-detectable reporter molecules and ions to evaluate diffusion in normal and ischemic brain. NMR Biomed 23:725-33
Shen, Gang; Fang, Huafeng; Song, Yinyin et al. (2009) Phospholipid conjugate for intracellular delivery of peptide nucleic acids. Bioconjug Chem 20:1729-36
Fang, Huafeng; Zhang, Ke; Shen, Gang et al. (2009) Cationic shell-cross-linked knedel-like (cSCK) nanoparticles for highly efficient PNA delivery. Mol Pharm 6:615-26
Wang, Rongsheng E; Kao, Jeffrey L-F; Hilliard, Carolyn A et al. (2009) Inhibition of heat shock induction of heat shock protein 70 and enhancement of heat shock protein 27 phosphorylation by quercetin derivatives. J Med Chem 52:1912-21
Lu, Jianyun; Dawson, Marcia I; Hu, Qiong Ying et al. (2009) The effect of antagonists on the conformational exchange of the retinoid X receptor alpha ligand-binding domain. Magn Reson Chem 47:1071-80
Bleeke, John R; Putprasert, Phawit; Thananatthanachon, Todsapon et al. (2008) Synthesis and Characterization of Fused-Ring Iridapyrroles. Organometallics 27:2744-5747
Su, Dian G T; Kao, Jeffrey L-F; Gross, Michael L et al. (2008) Structure determination of an interstrand-type cis-anti cyclobutane thymine dimer produced in high yield by UVB light in an oligodeoxynucleotide at acidic pH. J Am Chem Soc 130:11328-37
Oquare, Bereket Y; Taylor, John-Stephen (2008) Synthesis of peptide nucleic acid FRET probes via an orthogonally protected building block for post-synthetic labeling of peptide nucleic acids at the 5-position of uracil. Bioconjug Chem 19:2196-204

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