ANTIBODIES SPECIFIC FOR DISTINCT KV SUBUNITS UNVEIL A HETEROOLIGOMERIC BASIS FOR SUBTYPES OF ALPHA-DENDROTOXIN-SENSITIVE K+ CHANNELS IN BOVINE BRAIN

被引:140
作者
SCOTT, VES
MUNIZ, ZM
SEWING, S
LICHTINGHAGEN, R
PARCEJ, DN
PONGS, O
DOLLY, JO
机构
[1] UNIV LONDON IMPERIAL COLL SCI & TECHNOL, DEPT BIOCHEM, LONDON SW7 2AY, ENGLAND
[2] INST NEURALE SIGNALVERBEITUNG, ZENTRUM MOLEK NEUROBIOL, D-20246 HAMBURG, GERMANY
关键词
D O I
10.1021/bi00173a001
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
`The authentic subunit compositions of neuronal K+ channels purified from bovine brain were analyzed using a monoclonal antibody (mAb 5), reactive exclusively with the Kv1.2 subunit of the latter and polyclonal antibodies specific for fusion proteins containing C-terminal regions of four mammalian Kv proteins. Western blotting of the K+ channels isolated from several brain regions, employing the selective blocker alpha-dendrotoxin (alpha-DTX), revealed the presence in each of four different Kvs. Variable amounts of Kv1.1 and 1.4 subunits were observed in the K+ channels purified from cerebellum, corpus striatum, hippocampus, cerebral cortex, and brain stem; on the other hand, contents of Kv1.6 and 1.2 subunits appeared uniform throughout. Each Kv-specific antibody precipitated a different proportion (anti-Kv1.2 > 1.1 >> 1.6 > 1.4) of the channels detectable with radioiodinated alpha-DTX in every brain region, consistent with a widespread distribution of these oligomeric subtypes. Such heterooligomeric combinations were further documented by the lack of additivity upon their precipitation with a mixture of antibodies to Kv1.1 and Kv1.2; moreover, cross-blotting of the multimers precipitated by mAb 5 showed that they contain all four Kv proteins. Collectively, these findings demonstrate that subtypes of alpha-DTX-susceptible K+ channels are prevalent throughout mammalian brain which are composed of different K+ proteins assembled in complexes, shown previously to also contain auxiliary beta-subunits [Parcej, D. N., Scott, V. E. S., & Dolly, J. O. (1992) Biochemistry 31, 11084-11088].
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页码:1617 / 1623
页数:7
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共 38 条
[21]   CHARACTERIZATION OF MONOCLONAL-ANTIBODIES AGAINST VOLTAGE-DEPENDENT K+ CHANNELS RAISED USING ALPHA-DENDROTOXIN ACCEPTORS PURIFIED FROM BOVINE BRAIN [J].
MUNIZ, ZM ;
PARCEJ, DN ;
DOLLY, JO .
BIOCHEMISTRY, 1992, 31 (49) :12297-12303
[22]   LIGAND - A VERSATILE COMPUTERIZED APPROACH FOR CHARACTERIZATION OF LIGAND-BINDING SYSTEMS [J].
MUNSON, PJ ;
RODBARD, D .
ANALYTICAL BIOCHEMISTRY, 1980, 107 (01) :220-239
[24]   OLIGOMERIC PROPERTIES OF ALPHA-DENDROTOXIN-SENSITIVE POTASSIUM-ION CHANNELS PURIFIED FROM BOVINE BRAIN [J].
PARCEJ, DN ;
SCOTT, VES ;
DOLLY, JO .
BIOCHEMISTRY, 1992, 31 (45) :11084-11088
[25]   DISTRIBUTION OF ACCEPTORS FOR BETA-BUNGAROTOXIN IN THE CENTRAL NERVOUS-SYSTEM OF THE RAT [J].
PELCHENMATTHEWS, A ;
DOLLY, JO .
BRAIN RESEARCH, 1988, 441 (1-2) :127-138
[26]   DISTRIBUTION IN THE RAT CENTRAL NERVOUS-SYSTEM OF ACCEPTOR SUB-TYPES FOR DENDROTOXIN, A K+ CHANNEL PROBE [J].
PELCHENMATTHEWS, A ;
DOLLY, JO .
NEUROSCIENCE, 1989, 29 (02) :347-361
[27]   MOLECULAR-BIOLOGY OF VOLTAGE-DEPENDENT POTASSIUM CHANNELS [J].
PONGS, O .
PHYSIOLOGICAL REVIEWS, 1992, 72 (04) :S69-S88
[28]   THE RECEPTOR-SITE FOR THE BEE VENOM MAST-CELL DEGRANULATING PEPTIDE - AFFINITY LABELING AND EVIDENCE FOR A COMMON MOLECULAR TARGET FOR MAST-CELL DEGRANULATING PEPTIDE AND DENDROTOXIN-I, A SNAKE TOXIN ACTIVE ON K+ CHANNELS [J].
REHM, H ;
BIDARD, JN ;
SCHWEITZ, H ;
LAZDUNSKI, M .
BIOCHEMISTRY, 1988, 27 (06) :1827-1832
[29]   PURIFICATION AND SUBUNIT STRUCTURE OF A PUTATIVE K+-CHANNEL PROTEIN IDENTIFIED BY ITS BINDING-PROPERTIES FOR DENDROTOXIN-I [J].
REHM, H ;
LAZDUNSKI, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4919-4923
[30]   CLONING OF A BOVINE VOLTAGE-GATED K+ CHANNEL GENE UTILIZING PARTIAL AMINO-ACID-SEQUENCE OF A DENDROTOXIN-BINDING PROTEIN FROM BRAIN CORTEX [J].
REID, PF ;
PONGS, O ;
DOLLY, JO .
FEBS LETTERS, 1992, 302 (01) :31-34