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Research Article Free access | 10.1172/JCI107508
Calcium Research Laboratory, Veterans Administration Hospital, Kansas City, Missouri 64128
University of Missouri-Kansas City, School of Dentistry, Kansas City, Missouri 64108
University of Kansas, School of Medicine, Kansas City, Kansas 66103
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Calcium Research Laboratory, Veterans Administration Hospital, Kansas City, Missouri 64128
University of Missouri-Kansas City, School of Dentistry, Kansas City, Missouri 64108
University of Kansas, School of Medicine, Kansas City, Kansas 66103
Find articles by MacGregor, R. in: JCI | PubMed | Google Scholar
Calcium Research Laboratory, Veterans Administration Hospital, Kansas City, Missouri 64128
University of Missouri-Kansas City, School of Dentistry, Kansas City, Missouri 64108
University of Kansas, School of Medicine, Kansas City, Kansas 66103
Find articles by Liu, P. in: JCI | PubMed | Google Scholar
Calcium Research Laboratory, Veterans Administration Hospital, Kansas City, Missouri 64128
University of Missouri-Kansas City, School of Dentistry, Kansas City, Missouri 64108
University of Kansas, School of Medicine, Kansas City, Kansas 66103
Find articles by Hamilton, J. in: JCI | PubMed | Google Scholar
Calcium Research Laboratory, Veterans Administration Hospital, Kansas City, Missouri 64128
University of Missouri-Kansas City, School of Dentistry, Kansas City, Missouri 64108
University of Kansas, School of Medicine, Kansas City, Kansas 66103
Find articles by Cohn, D. in: JCI | PubMed | Google Scholar
Published December 1, 1973 - More info
Human parathyroid glands obtained at autopsy were incubated with [3H]leucine and [3H]lysine. After incubation, nonradioactive parathyroid tissue of either human or bovine origin was added. Radioactive parathyroid hormone and proparathyroid hormone were isolated from the gland and medium by organic solvent and salt fractionation, trichloroacetic acid precipitation, Sephadex G-100 gel filtration, and carboxymethyl cellulose column chromatography. The human hormonal peptides were identified in the ion-exchange column eluates by their relatively high levels of radioactivity, their elution positions, and their immunoreactivity to anti-PTH antiserum. The time-course of radioactive amino acid incorporation into these peptides and a brief incubation of the gland with radioactive amino acids, followed by various lengths of incubation with nonradioactive amino acids, indicated that a precursor-product relationship exists for the two peptides. An alternate method for isolation of the hormone and prohormone, which involves separation of peptides by urea-polyacrylamide gel electrophoresis, confirmed the identities of the human parathyroid hormone and proparathyroid hormone.