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Physicochemical analysis of reversible molybdate effects on different molecular forms of glucocorticoid receptor
Authors:T.William Hutchens  Francis S. Markland  Edward F. Hawkins
Affiliation:1. Department of Biochemistry, University of Southern California Los Angeles, CA 90033 USA;2. Department of Physiology and Biophysics University of Southern California Los Angeles, CA 90033 USA;3. the USC Comprehensive Cancer Center University of Southern California Los Angeles, CA 90033 USA
Abstract:Several distinct molecular forms of glucocorticoid receptor have been identified in a melanoma model system. We have used velocity sedimentation to monitor molybdate dependent alterations in receptor size and heterogeneity. In the absence of molybdate, native glucocorticoid receptor from dexamethasone-sensitive tumors sediments at 7–8 S and 12–13 S. Under identical conditions, receptor isolated from dexamethasone-resistant tumors sediments at 7–8 S only. However, when molybdate is introduced, either during homogenization or immediately prior to centrifugation, glucocorticoid receptors from both dexamethasone-sensitive and -resistant tumors sediment sharply at 9–10 S. These molybdate induced phenomena are reversible. The activated forms of glucocorticoid receptor isolated from both dexamethasone-sensitive and -resistant tumors by DEAE-cellulose chromatography have similar sedimentation coefficients (4–5 S) which are unaffected by molybdate.
Keywords:Author to whom correspondence should be addressed at: USC Cancer Center   Research Building I   1720 Zonal Avenue   Los Angeles   California 90033.
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