Gordon M. Walton

On the Mechanism of Action of ACTH

Publisher Summary This chapter focuses on the mechanism of action of adrenocorticotropic hormone (ACTH). The hormone stimulates steroidogenesis by a mechanism involving the synthesis of a protein with a rapid rate of turnover; the level of the protein then determines the rate of steroidogenesis. The experiments described in the chapter show that the inhibition of ACTH action by cycloheximide does not involve the inhibition of a step in the pathway prior to cholesterol but indicates that the antibiotic blocks steroidogenesis by preventing the further transformation of cholesterol in the pathway. The study presented in the chapter also demonstrates how the inhibition of protein synthesis blocked steroidogenesis by preventing the transformation of cholesterol to pregnenolone and the inhibitor had no effect on the other steps of the pathway. The injection of ACTH caused a marked decrease in adrenal cholesterol in association with its metabolism to the steroid hormones.

Ligand-induced endocytosis of the EGF receptor is blocked by mutational inactivation and by microinjection of anti-phosphotyrosine antibodies

Early events in ligand-induced endocytosis of the EGF receptor have been examined. A mutant EGF receptor devoid of intrinsic protein-tyrosine kinase activity bound EGF and dimerized normally yet failed to undergo ligand-induced internalization. Immunofluorescence microscopy revealed that receptors lacking kinase activity failed to undergo the ligand-induced internalization characteristic of receptors with kinase activity. Monoclonal anti-phosphotyrosine antibodies effectively inhibited phosphorylation of exogenous substrates in vitro and, when microinjected into cells containing active EGF receptors, prevented internalization of the receptor when cells were subsequently challenged with EGF. These results point to a crucial role for the kinase activity of the EGF receptor in the process of ligand-induced endocytosis of receptors, and imply that a phosphorylated substrate(s) is required.

Nucleotide regulation of a eukaryotic protein synthesis initiation complex

Formation of a ternary initiation complex containing Met-tRNAf, GTP and eukaryotic initiation factor 2, is the first step in sequential assembly of the initiation complex. The concentration of GTP required for half maximal formation of the ternary complex is 2.5 with 10(-6) M. GDP is a potent competitive inhibitor of ternary complex formation with Ki = 3.4 with 10(-7) M. The nucleotide binding site on eukaryotic initiation factor 2 demonstrates relative specificity for GDP with KD(GDP) = 3.0 with 10(-8) M; 100-fold higher concentrations of GTP than GDP are required for displacement of either [(3)H]GDP or [(3)h]gtp from the necleotide binding site. An ATP-dependent stimulation of ternary complex formation observed in partially purified initiation factor preparations is due to nucleoside diphosphate kinase (EC 2.7.4.6) which serves to remove inhibitory levels of GDP by phosphorylation with ATP. Since GTP is hydrolyzed to GDP during protein synthesis, this provides a mechanism by which the ATP:ADP ratio may regulate the rate of initiation of protein synthesis.

A three-step purification procedure for protein kinase C: Characterization of the purified enzyme

An efficient high yield three-step purification procedure for protein kinase C consisting of ion exchange, hydrophobic interaction, and substrate affinity chromatographies is described. Protein which appears homogeneous on sodium dodecyl sulfate-polyacrylamide gel electrophoresis contains amino acid sequences, predicted from cDNA cloning, for both the alpha and beta isoenzyme forms of the bovine brain enzyme. Both forms appear active as indicated by [3H]phorbol dibutyrate binding stoichiometry of approximately 1. Purified enzyme is active as a monomeric species, exhibits high cooperativity between Ca+2 and phosphatidylserine binding for activity, and undergoes intramolecular self-phosphorylation at both serine and threonine residues. Incubation of the enzyme with ATP, which leads to extensive self-phosphorylation, markedly stabilizes phosphotransferase activity without increasing the Vmax of the reaction.

Regulation of ternary [Met-tRNAf · GTP · eukaryotic initiation factor 2] protein synthesis initiation complex formation by the adenylate energy charge

Formation of the ternary [Met-tRNAf - GTP - eukaryotic initiation factor 2] protein synthesis initiation complex in rabbit reticulocyte ribosomal eluates is dependent on the GTP: GDP ratio and on the adenylate energy charge. The elements controlling ternary initiation complex formation have been studied in a reconstituted system contianing eukaryotic initiation factor 2 and nucleoside diphosphate kinase purified from the ribosomal eluate. The concentration of GTP required for half maximal formation of the ternary initiation complex is 2.5 - 10(6) M; GDP is a potent competitive inhibitor with Ki equals 3.4 - 10(7) M. Sensitive control of ternary initiation complex formation by the adenylate energy charge occurs through nucleoside diphosphate kinase regulation of the GTP : GDP ratio. Over a wide range of GTP : GDP ratios, 50% of maximal ternary initiation complex formation is observed at an adenylate energy charge of 0.85-0.90 resembling that seen in the unfractionated system. Small changes in adenylate energy charge near this value result in significant changes in the extent of ternary initiation complex formation. Since GTP is continually hydrolyzed to GDP during protein synthesis and since GDP is a competitive inhibitor of GTP binding to several of the protein factors necessary for mRNA translation, the synthetic process provides sensitive control by product inhibition. Ribosome-associated nucleoside diphosphate kinase control of GTP regeneration in response to the adenylate energy charge provides one mechanism for linking protein synthesis to the nutrient state and energy charge of the cell.

Preferential regulation of protein synthesis initiation complex formation by purine nucleotides.

A comparison of the affinities of eukaryotic initiation factor 2 and eukaryotic elongation factor 1 for GTP and GDP, and of the responses of initiation and elongation complex formation to various GTP mol fractions indicated that the initiation reaction was more sensitive to changes in the GTP: GDP ratio. In vitro regulation of the GTP: GDP ratio by the adenylate energy charge, a sensitive control parameter, also demonstrated a preference for regulation of formation of initiation complexes when compared to elongation complexes. These studies suggest that, based on the availability of energy, initiation is the rate-limiting step in the overall protein synthetic process.

The use of affinity chromatography in purification of cyclic nucleotide receptor proteins

Biospecific affinity chromatography has been used to purify specific cyclic AMP and cyclic GMP receptor proteins. Several variables are important for successful purification of the cyclic AMP receptor protein, the most critical being the length of the aliphatic spacer side arm. 8-(2-Aminoethyl)-amino-cyclic AMP coupled to the aliphatic spacer side arm. 8-(2-Aminoethyl)-amino-cyclic AMP coupled to agarose specifically retains the cyclic AMP receptor protein by interaction with the immobilized nucleotide. Binding of the cyclic AMP receptor subunit of cyclic AMP-dependent protein kinase to the immobilized nucleotide results in dissociation of the catalytic protein phosphokinase subunit which is not retained. The retained cyclic AMP receptor protein is subsequently eluted by cyclic AMP. Homogeneous cyclic AMP receptor protein prepared from rabbit skeletal muscle by affinity chromatography has been characterized. The molecular weight of the native protein as determined by analytical ultracentrifugation and polyacrylamide gel electrophoresis at varying acrylamide concentrations is 76 800 and 82 000, respectively. The protein is asymmetric with frictional and axial ratios of 1.64 and 12. SDS and urea polyacrylamide gel electrophoresis indicate that the native cyclic AMP receptor is composed of two identical subunits of 42 700 molecular weight. The native protein dimer binds 2 moles of cyclic AMP per mole of protein and is active in suppressing activity of isolated catalytic subunits of cyclic AMP-dependent protein kinase. Cyclic GMP receptor protein from bovine lung has been purified using the same affinity chromatography media. Since cyclic nucleotide binding to cyclic GMP-dependent protein kinase does not result in dissociation of regulatory receptor and catalytic phosphotransferase subunits, the cyclic GMP-dependent protein kinase holoenzyme is retained on the column and can be subsequently specifically eluted with cyclic GMP.

[51] The detection and characterization of cyclic AMP-receptor proteins in animal cells

Publisher Summary The filter binding assay can be used to quantitate the level of cAMP receptor protein present in a variety of tissues under a variety of growth and hormonal conditions. This method provides a convenient assay for detection in tissue extracts and for purification. It can be modified conveniently to study the kinetics of the interaction and the factors influencing this. Comparison of receptor activity with cAMP-dependent protein kinase activity is useful in evaluating the latter reaction. This method of receptor assay has also been modified to determine cAMP levels by competitive protein binding techniques.

[21] Protein modulation of cyclic nucleotide-dependent protein kinases

Publisher Summary This chapter describes protein modulation of cyclic nucleotide-dependent protein kinases. A poly(L-arginine) binding site has been identified on cGMP-dependent protein kinase and on the regulatory subunits of type I and type II cAMP-dependent protein kinases. Interaction of poly(L-arginine) with this site results in a time-, temperature-, and concentration-dependent inactivation of cyclic nucleotide binding activity. The presence of cyclic nucleotide at saturation concentrations protects cyclic nucleotide binding sites against inactivation. Poly(L-arginine) binding to cyclic nucleotide-dependent protein kinases affects kinase activity as well. The interaction of poly(L-arginine) with cGMP-dependent protein kinase results in a rapid activation of basal catalytic activity (assayed in the absence of cGMP) and a significant enhancement in the rate of autophosphorylation. The interaction of poly(L-arginine) with type II cAMP-dependent protein kinase stimulates autophosphorylation of the receptor subunit in the absence but not in the presence of cAMP.

Comparison of the interaction of cyclic nucleotide-dependent protein kinases with mononucleosomes and free histones

Arginine-rich histones H2A, H2B, H3 and H4 contain two regions of interaction with cyclic nucleotide-dependent protein kinases: a substrate phosphorylation site and a region which noncompetitively inhibits cyclic nucleotide binding to the protein kinases. We have compared the interaction of cyclic nucleotide-dependent protein kinases with these two sites in histones which are organized in nucleosome structures with the interaction of the enzymes with free histones. Whereas histones in solution are readily phosphorylated by cyclic GMP-dependent protein kinase and the catalytic subunit of cyclic AMP-dependent protein kinase, mononucleosomes are not phosphorylated by these enzymes. Histones extracted from mononucleosomes can be phosphorylated, indicating that the lack of phosphorylation of nucleosomes is not due to covalent modification of the histones but to their organization within the nucleosome structure. Whereas histones in solution are effective noncompetitive inhibitors of cyclic GMP binding to cyclic GMP-dependent protein kinase and of cyclic AMP binding to the regulatory subunits of cyclic AMP-dependent protein kinase, mononucleosomes do not affect cyclic nucleotide binding. These studies indicate that histones which are organized in nucleosome structures are neither substrates nor modifiers of cyclic nucleotide-dependent protein kinases.