Differentiation of Cl−/Ca2+-dependent and sodium dependent3H-glutamate binding to cortical membranes from rat brain by high energy radiation inactivation analysis
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Summary
The molecular weights of3H-L-glutamate binding in the presence of chloride and calcium ions and in the presence of sodium ions were determined by the high energy irradiation technique.
The molecular weight of sodium dependent3H-L-glutamate binding, which has pharmacological specificities similar to the high-affinity uptake system for L-glutamate, was 670,000 daltons.
The high-energy radiation inactivation study of chloride and calcium dependent and sodium independent3H-L-glutamate binding is consonant with the idea that, this binding represent glutamate transport into resealed plasma membrane vesicles.
Key words
3H-Glutamate binding, molecular target size glutamate uptake rat brainPreview
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References
- Balcar, V. J., Johnston, G. A. R.: Structural specificity of high affinity uptake of L-glutamate and L-aspartate by rat brain slices. J. Neurochem.19, 2657–2666 (1972).PubMedGoogle Scholar
- Baudry, M., Lynch, G.: Characterization of two [3H] glutamate binding sites in rat hippocampal membranes. J. Neurochem.36, 811–820 (1981).PubMedGoogle Scholar
- Fagg, G. E., Foster, A. C., Mena, E. E., Cotman, C. W.: Chloride and calcium ions reveal a pharmacologically-distinct population of L-glutamate binding sites in synaptic membranes: correspondence between biochemical and electrophysiological data. J. Neurosci.2, 958–965 (1982).PubMedGoogle Scholar
- Fagg, G. E., Foster, A. C., Mena, E. E., Cotman, C. W.: Chloride and calcium ions separate L-glutamate receptor populations in synaptic membranes. Europ. J. Pharmacol.88, 105–110 (1983 a).Google Scholar
- Fagg, G. E., Mena, E. E., Monaghan, D. T., Cotman, C. W.: Freezing eliminates a specific population of L-glutamate receptors in synaptic membranes. Neurosci. Lett.38, 157–162 (1983 b).PubMedGoogle Scholar
- Fagg, G. E., Matus, A.: Selective association of N-methyl aspartate and quisqualate types of L-glutamate receptor with brain postsynaptic densities. Proc. Natl. Acad. Sci. U.S.A.81, 6876–6880 (1984).PubMedGoogle Scholar
- Foster, A. C., Fagg, G. E.: Acidic amino acid binding sites in mammalian neuronal membranes: Their characteristics and relationship to synaptic receptors. Brain Res. Rev.7, 103–164 (1984).Google Scholar
- Honoré, T., Lauridsen, J.: Structural analogues of ibotenic acid. Synthesis of 4-methyl-homoibotenic acid and AMPA, including the crystal structure of AMPA monohydrate, Acta Chem. Scand.B 34, 235–240 (1980).Google Scholar
- Honoré, T., Nielsen, M.: Complex structure of quisqualate-sensitive glutamate receptors in rat cortex. Neurosci. Lett.54, 27–32 (1985).PubMedGoogle Scholar
- Jung, C. Y.: Molecular weight determination by radiation inactivation. In: Molecular and Chemical Characterization of Membrane Receptors (Venter, J. C., Harrison, L. C., eds.), pp. 193–208. New York: Alan R. Liss. 1984.Google Scholar
- Kepner, G. R., Macey, R. I.: Membrane enzyme systems. Molecular size determinations by radiation inactivation. Biochim. Biophys. Acta163, 188–203 (1968).PubMedGoogle Scholar
- Koerner J. F., Cotman, C. W.: L-2-amino-4-phosphonobutyric acid selectively inhibits perforant path synapses from lateral entorhinal cortex. Brain Res.216, 192–198 (1981).PubMedGoogle Scholar
- Kuhar, M. J., Zarbin, M. A.: Synaptosomal transport: a chloride dependence for choline, GABA, glycine and several other compounds. J. Neurochem.31, 251–256 (1978).PubMedGoogle Scholar
- Marvinzon, J. G., Mayor, F., Aragon, M. C., Gimenez, C., Valdivieso, F.: L-Aspartate transport into plasma membrane vesicles derived from rat brain synaptosomes. J. Neurochem.37, 1401–1406 (1981).PubMedGoogle Scholar
- Mena, E. E., Fagg, G. E., Cotman, C. W.: Chloride ions enhance L-glutamate binding to rat brain synaptic membranes. Brain Res.243, 378–381 (1982).PubMedGoogle Scholar
- Michaelis, E. K., Michaelis, M. L., Stormann, T. M., Chittenden, W. L., Grubbs, R. D.: Purification and molecular characterization of the brain synaptic membrane glutamate-binding protein. J. Neurochem.40, 1742–1753 (1983).PubMedGoogle Scholar
- Nielsen, M., Honoré, T., Braestrup, C.: Enhanced binding of the convulsive ligand, DMCM, to high-energy irradiated benzodiazepine receptors; evidence of complex receptor structure. Biochem. Pharmacol.32, 177–180 (1983).PubMedGoogle Scholar
- Nielsen, M., Braestrup, C.: The molecular target size of brain TBPS binding sites. Europ. J. Pharmacol.96, 321–322 (1983).Google Scholar
- Nielsen, M., Honoré, T., Braestrup, C.: Radiation inactivation of brain35S-TBPS binding sites reveals complicated molecular arrangements of the GABA/benzodiazepine receptor chloride channel complex. Biochem. Pharmacol.34, 3633–3642 (1985).PubMedGoogle Scholar
- Pin, J.-P., Bockaert, J., Recasens, M.: The Ca2+/Cl−-dependent Ca2+/Cl−-dependent L-[3H] glutamate binding: A new receptor or a particular transport process? FEBS Lett.175, 31–36 (1984).PubMedGoogle Scholar
- Schlegel, W.: Structure-function relationships for hormone receptors and adenyl cyclase: the contribution of target size analysis. J. Receptor Res.3, 399–357 (1983).Google Scholar
- Sharif, N. A., Roberts, P. J.: Problems associated with the binding of L-glutamic acid to synaptic membranes: Methodological aspects. J. Neurochem.34, 779–784 (1980).PubMedGoogle Scholar
- Slevin, J., Collins, J. F., Lindsley, K., Coyle, J. T.: Specific binding of [3H]glutamate to cerebellar membranes: evidence for recognition site heterogeneity. Brain Res.249, 353–360 (1982).PubMedGoogle Scholar
- Usherwood, P. N. R., Cull-Candy, S. G.: Distribution of glutamate sensitivity on insect muscle fibres. Neuropharmacology13, 455–461 (1974).PubMedGoogle Scholar
- Vincent, S. R., McGeer, E. G.: A comparison of sodium-dependent glutamate binding with high-affinity glutamate uptake in rat striatum. Brain Res.184, 99–108 (1980).PubMedGoogle Scholar
- Werling, L. L., Nadler, J. V.: Complex binding of L-[3H]glutamate to hippocampal synaptic membranes in the absence of sodium. J. Neurochem.38, 1050–1062 (1982).PubMedGoogle Scholar
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