JBC Transcription and Nuclear Factor Monoclonals

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Simons, S. S.
Right arrow Articles by Eisen, H. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Simons, S. S., Jr
Right arrow Articles by Eisen, H. J.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

J. Biol. Chem., Vol. 262, Issue 20, 9676-9680, 07, 1987

Identification of cysteine 656 as the amino acid of hepatoma tissue culture cell glucocorticoid receptors that is covalently labeled by dexamethasone 21-mesylate

SS Simons Jr, JG Pumphrey, S Rudikoff and HJ Eisen

Recent results using proteases suggest that dexamethasone 21-mesylate (Dex-Mes) labeling of the rat hepatoma tissue culture (HTC) cell glucocorticoid receptor occurs at one or a few closely grouped cysteine residues (Simons, S.S., Jr. (1987) J. Biol. Chem. 262, 9669-9675). In this study, a more direct approach was used both to establish that only one cysteine is labeled by [3H]Dex-Mes and to identify the amino acid sequence containing this labeled cysteine. Various analytical procedures did not provide the purification of the extremely hydrophobic Staphylococcus aureus V8 protease digestion fragment that is required for unique amino acid sequencing data. Therefore, Edman degradation was performed on the limit protease digest mixtures which appeared to contain only one 3H-labeled peptide. These degradation experiments revealed the number of amino acid residues between the NH2 terminus of each peptide and the [3H]Dex-Mes-labeled cysteine. A comparison of these amino acid spacings with the published amino acid sequence of the HTC cell glucocorticoid receptor (Miesfeld, R., Rusconi, S., Godowski, P. J., Maler, B. A., Okret, S., Wikstom, A-C., Gustafsson, J-A., and Yamamoto, K. R. (1986) Cell 46, 389-399) indicated that the one cysteine labeled by [3H]Dex-Mes is Cys-656. Further analysis of the receptor sequence for the presence of the observed grouping of proteolytic cleavage sites, but without any preconditions as to which amino acid was labeled, gave Asp-122 and Cys- 656 as the only two possibilities. Potential labeling of Asp-122 could be eliminated on the basis of immunological and genetic evidence. We, therefore, conclude that the single Dex-Mes-labeled site of the HTC cell glucocorticoid receptor has been identified as Cys-656. Since several lines of evidence indicate that [3H]Dex-Mes labeling of the receptor occurs in the steroid binding site, Cys-656 is the first amino acid which can be directly associated with a particular property of the glucocorticoid receptor.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
S. H. Meijsing, C. Elbi, H. F. Luecke, G. L. Hager, and K. R. Yamamoto
The Ligand Binding Domain Controls Glucocorticoid Receptor Dynamics Independent of Ligand Release
Mol. Cell. Biol., April 1, 2007; 27(7): 2442 - 2451.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
G. Giannoukos, D. Szapary, C. L. Smith, J. E. W. Meeker, and S. S. Simons Jr.
New Antiprogestins with Partial Agonist Activity: Potential Selective Progesterone Receptor Modulators (SPRMs) and Probes for Receptor- and Coregulator-Induced Changes in Progesterone Receptor Induction Properties
Mol. Endocrinol., February 1, 2001; 15(2): 255 - 270.
[Abstract] [Full Text]


Home page
Mol. Endocrinol.Home page
C. Logie, M. Nichols, K. Myles, J. W. Funder, and A. F. Stewart
Positive and Negative Discrimination of Estrogen Receptor Agonists and Antagonists Using Site-Specific DNA Recombinase Fusion Proteins
Mol. Endocrinol., August 1, 1998; 12(8): 1120 - 1132.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
K. J. Modarress, J. Opoku, M. Xu, N. J. Sarlis, and S. S. Simons Jr.
Steroid-induced Conformational Changes at Ends of the Hormone-binding Domain in the Rat Glucocorticoid Receptor Are Independent of Agonist Versus Antagonist Activity
J. Biol. Chem., September 19, 1997; 272(38): 23986 - 23994.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
W. B. Pratt and D. O. Toft
Steroid Receptor Interactions with Heat Shock Protein and Immunophilin Chaperones
Endocr. Rev., June 1, 1997; 18(3): 306 - 360.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
D. Szapary, M. Xu, and S. S. Simons Jr.
Induction Properties of a Transiently Transfected Glucocorticoid-responsive Gene Vary with Glucocorticoid Receptor Concentration
J. Biol. Chem., November 29, 1996; 271(48): 30576 - 30582.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
M. Xu, P. K. Chakraborti, M. J. Garabedian, K. R. Yamamoto, and S. S. Simons Jr.
Modular Structure of Glucocorticoid Receptor Domains Is Not Equivalent to Functional Independence. STABILITY AND ACTIVITY OF THE STEROID BINDING DOMAIN ARE CONTROLLED BY SEQUENCES IN SEPARATE DOMAINS
J. Biol. Chem., August 30, 1996; 271(35): 21430 - 21438.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. F. Stancato, A. M. Silverstein, C. Gitler, B. Groner, and W. B. Pratt

J. Biol. Chem., April 12, 1996; 271(15): 8831 - 8836.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Nakajima, J.-C. Hsieh, P. W. Jurutka, M. A. Galligan, C. A. Haussler, G. K. Whitfield, and M. R. Haussler
Examination of the Potential Functional Role of Conserved Cysteine Residues in the Hormone Binding Domain of the Human 1,25-Dihydroxyvitamin D(3) Receptor
J. Biol. Chem., March 1, 1996; 271(9): 5143 - 5149.
[Abstract] [Full Text] [PDF]


Home page
ANN INTERN MEDHome page
G. P. Chrousos, S. D. Detera-Wadleigh, and M. Karl
Syndromes of Glucocorticoid Resistance
Ann Intern Med, December 1, 1993; 119(11): 1113 - 1124.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1987 by the American Society for Biochemistry and Molecular Biology.