Characterization and purification of the Drosophila Kc cell JH binding protein
Juvenile hormone (JH) is one of the principal regulators of insect development. First, physical properties of the JH binding protein are characterized using a photoaffinity ligand ({sup 3}H)-EFDA. Second, ({sup 3}H)-EFDA is employed as labeled to examined the behavior of the JH binding protein in several protein separation procedures. The properties of heparin-agarose, hydroxylapatite, gel filtration, ion exchange, and chromatofocusing chromatography are examined for their ability to affect separation of the JH binding protein from other components of Kc cell cytosol. Third, several of the separation procedures are linked sequentially into a JH binding protein purification scheme and the procedure is shown to purify the JH binding protein to homogeneity. Fourth, competition study is carried out to demonstrate the protein purified using ({sup 3}H)-EFDA is JH competable. In addition, JH III, the naturally occurring hormone, is used as the radioligand in this purification procedure, the authenticity of the intracellar JH binding protein is reassured. Fifth, the amino acid composition of the JH binding protein is elucidated. Finally, nanomoles of the purified JH binding protein are collected for protein microsequencing. The sequencing data will be used to synthesize peptide which, in turn, will be used for JH binding protein antibody production.
- Research Organization:
- California Univ., Los Angeles, CA (USA)
- OSTI ID:
- 6159584
- Resource Relation:
- Other Information: Thesis (Ph. D.)
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
PROTEINS
CHEMICAL COMPOSITION
AMINO ACID SEQUENCE
CHROMATOGRAPHY
DROSOPHILA
FRACTIONATION
HORMONES
LIGANDS
PHYSICAL PROPERTIES
TRACER TECHNIQUES
TRITIUM COMPOUNDS
ANIMALS
ARTHROPODS
DIPTERA
FLIES
FRUIT FLIES
HYDROGEN COMPOUNDS
INSECTS
INVERTEBRATES
ISOTOPE APPLICATIONS
MOLECULAR STRUCTURE
ORGANIC COMPOUNDS
SEPARATION PROCESSES
550201* - Biochemistry- Tracer Techniques