Open AccessEffect of chemical inactivating agents on glucocorticoid receptor proteins in mouse and hamster cells.
Author(s) -
Howard A. Young,
Wade P. Parks,
Edward M. Scolnick
Publication year - 1975
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.72.8.3060
Subject(s) - iodoacetamide , cytosol , glucocorticoid receptor , hamster , receptor , biochemistry , glucocorticoid , hormone , hormone receptor , steroid hormone , chemistry , n ethylmaleimide , steroid hormone receptor , biology , endocrinology , estrogen receptor , enzyme , cysteine , genetics , cancer , breast cancer
The ffect of N-ethylmaleimide and iodoacetamide on the glucocorticoid receptor activity extracted from the cytosol of either mouse of hamster cells has been investigated. Treatment of mouse or hamster cytosol with N-ethylmaleimide or iodoacetamide rapidly inactivates the [3H]glucocorticoid hormone binding activity of either cytosol. Prebinding the glucocorticoid hormone, dexamethasone, to the cytosol receptor blocks the rapid inactivation of the receptor by N-ethylmaleimide. Treatment of the prebound hormone-receptor complex with iodoacetamide prevents the subsequent binding of the hormone-receptor complex to DNA without causing a dissociation of the complex. Although the conclusions may be limited by the lack of purity of the receptor, the results suggest that a sulfhydryl group is involved in the binding of glucocorticoid hormones to the receptor protein. In addition, the results suggest that iodoacetamide is inactivating a separate chemical site which is necessary for the binding of the hormone-receptor complex to DNA.