Purification and immunochemical characterization of the cytoplasmic androgen-binding protein of rat liver
- Univ. of Texas Health Science Center, San Antonio (USA)
The cytoplasmic androgen-binding (CAB) protein of the male rate liver has been implicated to play a role in the androgen-dependent regulation of {alpha}{sub 2u}-globulin synthesis. The liver of the adult male rat contains about 50 fmol of specific high-affinity androgen-binding activity per milligram of total cytosolic protein. Photoaffinity labeling with ({sup 3}H)R-1881 followed by SDS-polyacrylamide gel electrophoresis and autoradiography shows that the CAB is a 31-kilodalton protein. By means of DEAE-cellulose chromatography and preparative SCS-polyacrylamide gel electrophoresis, the authors have purified the CAB protein to electrophoretic homogeneity and have raised polyclonal rabbit antiserum that is monospecific to this protein. In the sucrose density gradient, the antiserum reacted with the androgen-binding component of the male liver cytosol prelabeled with tritiated dihydrotestosterone. Western blot analysis of the liver cytosol showed that the antiserum recognizes only the 31-kDa androgen-binding component. Such immunoblotting also showed that unlike the young adult, the androgen-insensitive states during prepuberty and senescence are associated with a marked reduction in the hepatic concentration of the immunoreactive CAB protein. No immunochemical cross-reactivity between CAB and another androgen-binding component of M{sub r} 29K was observed. The latter finding favors the possibility that 31- and 29-kDa androgen-binding components may have distinct sequence structure.
- OSTI ID:
- 5601316
- Journal Information:
- Biochemistry; (USA), Journal Name: Biochemistry; (USA) Vol. 28:4; ISSN 0006-2960; ISSN BICHA
- Country of Publication:
- United States
- Language:
- English
Similar Records
Cytoplasmic androgen binding protein of rat liver: molecular characterization after photoaffinity labeling and functional correlation with the age-dependent synthesis of alpha 2u-globulin
Partial purification of a binding protein for polychlorinated biphenyls from rat lung cytosol: Physicochemical and immunochemical characterization
Comparative characterization of thyroid hormone receptors and binding proteins in rat liver nucleus, plasma membrane, and cytosol by photoaffinity labeling with L-thyroxine
Journal Article
·
Tue Jun 30 00:00:00 EDT 1987
· Biochemistry; (United States)
·
OSTI ID:5727503
Partial purification of a binding protein for polychlorinated biphenyls from rat lung cytosol: Physicochemical and immunochemical characterization
Journal Article
·
Tue Oct 04 00:00:00 EDT 1988
· Biochemistry; (USA)
·
OSTI ID:6831838
Comparative characterization of thyroid hormone receptors and binding proteins in rat liver nucleus, plasma membrane, and cytosol by photoaffinity labeling with L-thyroxine
Journal Article
·
Tue Sep 10 00:00:00 EDT 1985
· Biochemistry; (United States)
·
OSTI ID:5965917
Related Subjects
550201* -- Biochemistry-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
AMINO ACID SEQUENCE
ANDROGENS
ANDROSTANES
ANIMALS
BIOCHEMISTRY
BODY
CHEMICAL REACTIONS
CHEMISTRY
CROSS-LINKING
CYTOCHEMISTRY
DIGESTIVE SYSTEM
ELECTROPHORESIS
GLANDS
HORMONES
HYDROGEN COMPOUNDS
IMMUNE SERUMS
IMMUNOLOGY
LIVER
MAMMALS
MOLECULAR STRUCTURE
ORGANIC COMPOUNDS
ORGANS
POLYMERIZATION
PROTEINS
PURIFICATION
RATS
RODENTS
STEROID HORMONES
STEROIDS
TRITIUM COMPOUNDS
VERTEBRATES
59 BASIC BIOLOGICAL SCIENCES
AMINO ACID SEQUENCE
ANDROGENS
ANDROSTANES
ANIMALS
BIOCHEMISTRY
BODY
CHEMICAL REACTIONS
CHEMISTRY
CROSS-LINKING
CYTOCHEMISTRY
DIGESTIVE SYSTEM
ELECTROPHORESIS
GLANDS
HORMONES
HYDROGEN COMPOUNDS
IMMUNE SERUMS
IMMUNOLOGY
LIVER
MAMMALS
MOLECULAR STRUCTURE
ORGANIC COMPOUNDS
ORGANS
POLYMERIZATION
PROTEINS
PURIFICATION
RATS
RODENTS
STEROID HORMONES
STEROIDS
TRITIUM COMPOUNDS
VERTEBRATES