To complement Emory University's rapidly expanding strength in molecular biology, we propose to establish a """"""""Microchemical Analysis Facility for Molecular Biology."""""""" This facility is designed to provide Emory and greater Atlanta scientists with access to modern molecular biological techniques and materials that require instruments too costly for individual laboratories to purchase and operate. The facility would consist of an oligonucleotide synthesizer, a peptide synthesizer, and a polypeptide sequencher purchased with federal funds and an amino acid analyzer, a microcomputer with molecular biology software, an autoradiograph processor, a spectrophotometer, a pH meter and balancer, refrigerators and freezers, electrophoresis equipment, remodeled space, and start-up funds to be provided by Emory Medical School and Emory University. The facility will be designed to provide users: (1) quality oligonucleotides, (2) quality synthetic peptides, (3) accurate peptide sequences, and (4) computer resources for molecular biology, on a fee-for-service basis. The instruments will run by a full-time Ph.D. level operator and the accounts maintained by a facility secretary. The facility will be administered by the Principal Investigator (""""""""Director""""""""), an """"""""Advisory Committee"""""""" of four senior faculty and an """"""""Applications Committee"""""""" of five senior faculty including a laboratory coordinator and an experienced supervisor for each instrument. The primary user group will include 19 NIH funded scientists with a total direct costs funding of over $3,000,000. Additional users will be drawn form other Emory and Atlanta scientists. Establishing this facility would have a catalytic effect on molecular biological research at Emory and significantly advance biotechnology in the Southeast.

Project Start
1986-05-01
Project End
1988-04-30
Budget Start
1986-05-01
Budget End
1988-04-30
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Emory University
Department
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Lee, Choon-Myung; Pohl, Jan; Morgan, Edward T (2009) Dual mechanisms of CYP3A protein regulation by proinflammatory cytokine stimulation in primary hepatocyte cultures. Drug Metab Dispos 37:865-72
Binda, Claudia; Wang, Jin; Li, Min et al. (2008) Structural and mechanistic studies of arylalkylhydrazine inhibition of human monoamine oxidases A and B. Biochemistry 47:5616-25
Khwaja, F W; Svoboda, P; Reed, M et al. (2006) Proteomic identification of the wt-p53-regulated tumor cell secretome. Oncogene 25:7650-61
Hubalek, Frantisek; Binda, Claudia; Li, Min et al. (2004) Inactivation of purified human recombinant monoamine oxidases A and B by rasagiline and its analogues. J Med Chem 47:1760-6
Hubalek, Frantisek; Pohl, Jan; Edmondson, Dale E (2003) Structural comparison of human monoamine oxidases A and B: mass spectrometry monitoring of cysteine reactivities. J Biol Chem 278:28612-8
Ceman, Stephanie; O'Donnell, William T; Reed, Matt et al. (2003) Phosphorylation influences the translation state of FMRP-associated polyribosomes. Hum Mol Genet 12:3295-305
Lee, E-H; Rouquette-Loughlin, C; Folster, J P et al. (2003) FarR regulates the farAB-encoded efflux pump of Neisseria gonorrhoeae via an MtrR regulatory mechanism. J Bacteriol 185:7145-52
Hubalek, Frantisek; Edmondson, Dale E; Pohl, Jan (2002) Synthesis and characterization of a collagen model delta-O-phosphohydroxylysine-containing peptide. Anal Biochem 306:124-34
Li, Min; Hubalek, Frantisyyk; Newton-Vinson, Paige et al. (2002) High-level expression of human liver monoamine oxidase A in Pichia pastoris: comparison with the enzyme expressed in Saccharomyces cerevisiae. Protein Expr Purif 24:152-62
Cai, Z; Saugstad, J A; Sorensen, S D et al. (2001) Cyclic AMP-dependent protein kinase phosphorylates group III metabotropic glutamate receptors and inhibits their function as presynaptic receptors. J Neurochem 78:756-66

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