Literature DB >> 3882886

Two forms of rat brain glutamic acid decarboxylase differ in their dependence on free pyridoxal phosphate.

L A Denner, J Y Wu.   

Abstract

There are two forms of glutamate decarboxylase (GAD) found in the rat brain. One form (form A) does not require exogenous pyridoxal-5'-phosphate (PLP) for activity whereas another form (form B) requires exogenous PLP for activity. These two forms differ greatly in temperature sensitivity, inactivation, and reactivation by the removal and readdition of PLP, electrophoretic mobility, and regional distribution. For instance, forms A and B are inactivated to an extent of 91% and 10%, respectively, by the treatment at 45 degrees C for 30 min; form A is greatly inactivated (77%) by the removal of PLP by aminooxyacetic acid and the readdition of PLP, whereas form B is only slightly inactivated (7%). Forms A and B can be clearly separated by 5% polyacrylamide gel electrophoresis in which form A migrates faster than form B. In all 10 brain regions studied, form A is present in smaller amounts than form B. This difference is greatest in the superior colliculus (the ratio of B to A is about 5), while in the locus coeruleus and cerebellum, forms A and B are present in nearly equal proportion. Forms A and B are similar with respect to relative abundance in hypotonic, isotonic, and hypertonic preparations, inhibition of catalytic activity by a carbonyl-trapping agent, immunochemical properties, and chromatographic patterns in a variety of systems. The significance of forms A and B and PLP in the regulation of gamma-amino-butyric acid (GABA) level is also discussed.

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Year:  1985        PMID: 3882886     DOI: 10.1111/j.1471-4159.1985.tb12910.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  14 in total

1.  Comparative study between 4-aminobutyrate-2-oxoglutarate aminotransferase (GABA-T) from rat forebrain and cerebellum.

Authors:  C Arce; S Cañadas; M De Vicente; M J Oset-Gasque; M P González
Journal:  Neurochem Res       Date:  1992-07       Impact factor: 3.996

2.  Isolation and characterization of endogenous modulators for GABA system.

Authors:  M Yarom; J Bao; X W Tang; E Wu; Y H Lee; W H Tsai; J Y Wu
Journal:  Neurochem Res       Date:  1992-01       Impact factor: 3.996

3.  Is there a high molecular weight glutamic acid decarboxylase?

Authors:  M Pérez-de la Mora; A B Rizo-Silva; J Méndez-Franco
Journal:  Neurochem Res       Date:  1992-04       Impact factor: 3.996

4.  Molecular cloning and amino acid sequence of brain L-glutamate decarboxylase.

Authors:  W M Huang; L Reed-Fourquet; E Wu; J Y Wu
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

Review 5.  The structural and functional heterogeneity of glutamic acid decarboxylase: a review.

Authors:  M G Erlander; A J Tobin
Journal:  Neurochem Res       Date:  1991-03       Impact factor: 3.996

Review 6.  Regulatory properties of brain glutamate decarboxylase.

Authors:  D L Martin
Journal:  Cell Mol Neurobiol       Date:  1987-09       Impact factor: 5.046

7.  Structure and function of L-glutamate decarboxylase.

Authors:  J Y Wu; W M Huang; L Reed-Fourquet; J Bao; B Nathan; E Wu; W H Tsai
Journal:  Neurochem Res       Date:  1991-03       Impact factor: 3.996

8.  Postnatal expression of glutamate decarboxylases in developing rat cerebellum.

Authors:  K F Greif; M G Erlander; N J Tillakaratne; A J Tobin
Journal:  Neurochem Res       Date:  1991-03       Impact factor: 3.996

9.  Basal Ganglia circuits underlying the pathophysiology of levodopa-induced dyskinesia.

Authors:  Pedro Barroso-Chinea; Erwan Bezard
Journal:  Front Neuroanat       Date:  2010-09-14       Impact factor: 3.856

10.  Cloning, characterization, and autoimmune recognition of rat islet glutamic acid decarboxylase in insulin-dependent diabetes mellitus.

Authors:  B K Michelsen; J S Petersen; E Boel; A Møldrup; T Dyrberg; O D Madsen
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

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