This proposal is to provide continuation support for research into applications of mass spectrometry in Endocrinology and Metabolism. This research will include five objectives: (1) basic developmental research into mass spectrometry of hormonal peptides, proteins and steroids; (2) collaborative studies on investigation of steroid biosynthesis and metabolism in patients with endocrinopathies; (3) studies of in vitro metabolism of steroids in cellular or enzyme preparations; (4) characterization of proteins and glycoproteins of importance in steroid and metabolic research and (5) metabolic studies using stable isotopes. We are in a unique position to forward the first objective (development research). During the tenure of the current grant we were successful on two occasions (1987, 1991) in obtaining new mass spectrometers through the Shared Instrumentation Grant program (thermospray/FAB quadrupole mass spectrometer, electrospray HPLC/MS). These instruments in addition to our GC/MS allow us to analyze a full complement of analytes from unconjugated steroids through polar steroid conjugates and hormonal peptides to intact proteins. The increased capabilities of our facility will permit us to enter new fields. In one instance we want to develop new mass spectrometric methods based on the new electrospray MS technique. This will include combining micro- or capillary HPLC with the new instrumentation. Using this technology it may be possible to achieve the sensitivity required to determined intact steroid conjugates of clinical importance (e.g. androstanediol glucuronide). The availability of electrospray MS will allow us to enter the protein identification area since analysis of both intact proteins, tryptic peptides and determination of glycoprotein structures will be possible. Combination with micro- or capillary HPLC will allow this to be conducted on picomole amounts of components.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK034400-09
Application #
3232734
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1984-01-01
Project End
1994-12-31
Budget Start
1992-01-13
Budget End
1992-12-31
Support Year
9
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Children's Hospital & Res Ctr at Oakland
Department
Type
DUNS #
City
Oakland
State
CA
Country
United States
Zip Code
94609
Witkowski, A; Witkowska, H E; Knudsen, J et al. (1999) Ether bond cleavage in an arylazido photoaffinity probe induced by ultraviolet light. Anal Biochem 267:412-5
Carr, A C; van den Berg, J J; Winterbourn, C C (1998) Differential reactivities of hypochlorous and hypobromous acids with purified Escherichia coli phospholipid: formation of haloamines and halohydrins. Biochim Biophys Acta 1392:254-64
Santner, S J; Albertson, B; Zhang, G Y et al. (1998) Comparative rates of androgen production and metabolism in Caucasian and Chinese subjects. J Clin Endocrinol Metab 83:2104-9
Rangan, V S; Serre, L; Witkowska, H E et al. (1997) Characterization of the malonyl-/acetyltransacylase domain of the multifunctional animal fatty acid synthase by expression in Escherichia coli and refolding in vitro. Protein Eng 10:561-6
Bearer, C; Emerson, R K; O'Riordan, M A et al. (1997) Maternal tobacco smoke exposure and persistent pulmonary hypertension of the newborn. Environ Health Perspect 105:202-6
Hellerstein, M K; Letscher, A; Schwarz, J M et al. (1997) Measurement of hepatic Ra UDP-glucose in vivo in rats: relation to glycogen deposition and labeling patterns. Am J Physiol 272:E155-62
Hellerstein, M K; Wu, K; McGrath, M et al. (1996) Effects of dietary n-3 fatty acid supplementation in men with weight loss associated with the acquired immune deficiency syndrome: Relation to indices of cytokine production. J Acquir Immune Defic Syndr Hum Retrovirol 11:258-70
Hegy, G B; Shackleton, C H; Carlquist, M et al. (1996) Carboxymethylation of the human estrogen receptor ligand-binding domain-estradiol complex: HPLC/ESMS peptide mapping shows that cysteine 447 does not react with iodoacetic acid. Steroids 61:367-73
Rangan, V S; Smith, S (1996) Expression in Escherichia coli and refolding of the malonyl-/acetyltransferase domain of the multifunctional animal fatty acid synthase. J Biol Chem 271:31749-55
Walker, B R; Best, R; Shackleton, C H et al. (1996) Increased vasoconstrictor sensitivity to glucocorticoids in essential hypertension. Hypertension 27:190-6

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