Proceedings of the National Academy of Sciences · 1977 · 83 citations · 20 references
Life SciencesBiochemistryEndocrinologyHormone BiochemistryReproductive EndocrinologySteroid BiochemistryAffinity ChromatographyHormone Binding ProteinsHormone ReceptorsHormone SignalingSteroid Hormone BiochemistrySteroid Hormone SignalingAffinity Purification Of Binding ProteinsCalcium-dependent Enzyme ActivationEstrogen ReceptorsGel ElectrophoresisHormone Receptor Binding ProteinsIsoelectric PointNative Polyacrylamide Gel ElectrophoresisPolyacrylamide Gel Electrophoresis
Heparin attached covalently to agarose beads binds the "native" form of the estradiol receptor with very high affinity. Chondroitin sulfate does not bind to the receptor. When the receptor is complexed with hormone, the affinity is at least 10 times higher. Only the "native" and not the "nuclear" or the "derived" (i.e., after activation by a calcium-dependent enzyme) forms of the estradiol receptor interact with heparin. The "native" estradiol-receptor complex is purified to homogeneity after chromatography on columns of heparin-agarose, Sephadex G-200, and DEAE-cellulose, followed by two more Sephadex G-200 columns. The purified molecule is a single polypeptide of molecular weight 69,000 by polyacrylamide gel electrophoresis in sodium dodecyl sulphate. The sedimentation coefficient on sucrose gradients is 4.3 S, the Stokes radius from gel filtration is 36.5 A, and the isoelectric point is 6.4. The purified [3H]estradiol-receptor complex exchanges the radioactive hormone with estradiol or other estrogenic steroids, but not with testosterone, 5alpha-dihydrotestosterone, or progesterone.
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A modified uronic acid carbazole reaction
Thomas Bitter, H. M. Muir · Analytical Biochemistry · 1962 · 6.3K citations
Protein Purification by Affinity Chromatography
Pedro Cuatrecasas · Journal of Biological Chemistry · 1970 · 2.8K citations · Full text