A novel method for expression and large-scale production of human brain L-glutamate decarboxylase

被引:25
作者
Davis, KM
Foos, T
Bates, CS
Tucker, E
Hsu, CC
Chen, WQ
Jin, H
Tyburski, JB
Schloss, JV
Tobin, AJ
Wu, JY
机构
[1] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Med Chem, Lawrence, KS 66045 USA
[3] Univ Calif Los Angeles, Dept Biol, Los Angeles, CA 90024 USA
[4] Acad Sinica, Inst Biol Chem, Taipei, Taiwan
基金
美国国家科学基金会;
关键词
D O I
10.1006/bbrc.1999.2038
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
L-Glutamate decarboxylase (GAD; EC 4.1.1.15) is the rate-limiting enzyme involved in the synthesis of gamma-aminobutyric acid (GABA), the major inhibitory neurotransmitter in the mammalian brain, Imbalance in the conversion of glutamate to GABA has been implicated in a host of human diseases, Studies on the structure, function, and therapeutic use of GAD have been precluded by insufficient quantities of purified active enzyme. Here we report a novel methodology for the expression and large-scale production of enzymatically active, pure, recombinant human GAD65 and GAD67. This method circumvents the sequestering of expressed protein into insoluble inclusion bodies and reduces production of truncated proteins. The availability of sufficient quantities of purified HGAD65 and HGAD67 has allowed for the production of specific polyclonal antibodies that discriminate between the two isoforms. This methodology, in addition to providing key human brain enzymes, may be generally applicable to other systems. (C) 2000 Academic Press.
引用
收藏
页码:777 / 782
页数:6
相关论文
共 22 条
  • [1] IDENTIFICATION OF THE 64K AUTOANTIGEN IN INSULIN-DEPENDENT DIABETES AS THE GABA-SYNTHESIZING ENZYME GLUTAMIC-ACID DECARBOXYLASE
    BAEKKESKOV, S
    AANSTOOT, HJ
    CHRISTGAU, S
    REETZ, A
    SOLIMENA, M
    CASCALHO, M
    FOLLI, F
    RICHTEROLESEN, H
    CAMILLI, PD
    [J]. NATURE, 1990, 347 (6289) : 151 - 156
  • [2] BRAIN L-GLUTAMATE DECARBOXYLASE - INHIBITION BY PHOSPHORYLATION AND ACTIVATION BY DEPHOSPHORYLATION
    BAO, J
    CHEUNG, WY
    WU, JY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (12) : 6464 - 6467
  • [3] 2 HUMAN GLUTAMATE DECARBOXYLASES, 65-KDA GAD AND 67-KDA GAD, ARE EACH ENCODED BY A SINGLE GENE
    BU, DF
    ERLANDER, MG
    HITZ, BC
    TILLAKARATNE, NJK
    KAUFMAN, DL
    WAGNERMCPHERSON, CB
    EVANS, GA
    TOBIN, AJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (06) : 2115 - 2119
  • [4] DAVIDSON N, 1976, NEUROTRANSMITTER AMI, P6
  • [5] STRESS-INDUCED BEHAVIORAL DEPRESSION IN THE RAT IS ASSOCIATED WITH A DECREASE IN GABA RECEPTOR-MEDIATED CHLORIDE-ION FLUX AND BRAIN BENZODIAZEPINE RECEPTOR OCCUPANCY
    DRUGAN, RC
    MORROW, AL
    WEIZMAN, R
    WEIZMAN, A
    DEUTSCH, SI
    CRAWLEY, JN
    PAUL, SM
    [J]. BRAIN RESEARCH, 1989, 487 (01) : 45 - 51
  • [6] 2 GENES ENCODE DISTINCT GLUTAMATE DECARBOXYLASES
    ERLANDER, MG
    TILLAKARATNE, NJK
    FELDBLUM, S
    PATEL, N
    TOBIN, AJ
    [J]. NEURON, 1991, 7 (01) : 91 - 100
  • [7] Role of synaptic vesicle proton gradient and protein phosphorylation on ATP-mediated activation of membrane-associated brain glutamate decarboxylase
    Hsu, CC
    Thomas, C
    Chen, WQ
    Davis, KM
    Foos, T
    Chen, JL
    Wu, E
    Floor, E
    Schloss, JV
    Wu, JY
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (34) : 24366 - 24371
  • [8] Epilepsy in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase
    Kash, SF
    Johnson, RS
    Tecott, LH
    Noebels, JL
    Mayfield, RD
    Hanahan, D
    Baekkeskov, S
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (25) : 14060 - 14065
  • [9] SPONTANEOUS LOSS OF T-CELL TOLERANCE TO GLUTAMIC-ACID DECARBOXYLASE IN MURINE INSULIN-DEPENDENT DIABETES
    KAUFMAN, DL
    CLARESALZLER, M
    TIAN, JD
    FORSTHUBER, T
    TING, GSP
    ROBINSON, P
    ATKINSON, MA
    SERCARZ, EE
    TOBIN, AJ
    LEHMANN, PV
    [J]. NATURE, 1993, 366 (6450) : 69 - 72
  • [10] GABAergic deafferentation hypothesis of brain aging and Alzheimer's disease revisited
    Marczynski, TJ
    [J]. BRAIN RESEARCH BULLETIN, 1998, 45 (04) : 341 - 379