SUBUNIT-SPECIFIC BLOCK OF CLONED NMDA RECEPTORS BY ARGIOTOXIN636

被引:55
作者
RADITSCH, M
RUPPERSBERG, JP
KUNER, T
GUNTHER, W
SCHOEPFER, R
SEEBURG, PH
JAHN, W
WITZEMANN, V
机构
[1] MAX PLANCK INST MED RES,ZELLPHYSIOL ABT,JAHNSTR 29,W-6900 HEIDELBERG 1,GERMANY
[2] UNIV HEIDELBERG,CTR MOLEC BIOL,W-6900 HEIDELBERG,GERMANY
[3] MAX PLANCK INST MED RES,BIOPHYS ABT,W-6900 HEIDELBERG 1,GERMANY
关键词
NMDA RECEPTOR; RECOMBINANT; ARGIOTOXIN; SITE-DIRECTED MUTAGENESIS;
D O I
10.1016/0014-5793(93)81533-6
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
Cloned NMDA receptor channels of the NR1-NR2A, NR1-NR2B and NR1-NR2C type show differences in argiotoxin636 block. Mutations of an asparagine residue located at a homologous position in the TM2 region of all NMDA receptor subunits, which corresponds to the Q/R site of the AMPA receptors, alters the argiotoxin636-induced block. The results suggest that the toxin interacts at this amino acid position with the putative pore forming TM2 region of the NMDA receptor subunits. Sequence differences in the TM2 segment of NR2A and NR2C subunits are not responsible for the subtype-specific sensitivity to argiotoxin636 as revealed by site-directed mutagenesis.
引用
收藏
页码:63 / 66
页数:4
相关论文
共 18 条
[1]   STRUCTURES AND BIOLOGICAL-ACTIVITIES OF 3 SYNAPTIC ANTAGONISTS FROM ORB WEAVER SPIDER VENOM [J].
ADAMS, ME ;
CARNEY, RL ;
ENDERLIN, FE ;
FU, ET ;
JAREMA, MA ;
LI, JP ;
MILLER, CA ;
SCHOOLEY, DA ;
SHAPIRO, MJ ;
VENEMA, VJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (02) :678-683
[2]   DIVALENT ION PERMEABILITY OF AMPA RECEPTOR CHANNELS IS DOMINATED BY THE EDITED FORM OF A SINGLE SUBUNIT [J].
BURNASHEV, N ;
MONYER, H ;
SEEBURG, PH ;
SAKMANN, B .
NEURON, 1992, 8 (01) :189-198
[3]   CONTROL BY ASPARAGINE RESIDUES OF CALCIUM PERMEABILITY AND MAGNESIUM BLOCKADE IN THE NMDA RECEPTOR [J].
BURNASHEV, N ;
SCHOEPFER, R ;
MONYER, H ;
RUPPERSBERG, JP ;
GUNTHER, W ;
SEEBURG, PH ;
SAKMANN, B .
SCIENCE, 1992, 257 (5075) :1415-1419
[4]   ARGIOTOXIN636 INHIBITS NMDA-ACTIVATED ION CHANNELS EXPRESSED IN XENOPUS OOCYTES [J].
DRAGUHN, A ;
JAHN, W ;
WITZEMANN, V .
NEUROSCIENCE LETTERS, 1991, 132 (02) :187-190
[5]   STRUCTURE AND SYNTHESIS OF A POTENT GLUTAMATE RECEPTOR ANTAGONIST IN WASP VENOM [J].
ELDEFRAWI, AT ;
ELDEFRAWI, ME ;
KONNO, K ;
MANSOUR, NA ;
NAKANISHI, K ;
OLTZ, E ;
USHERWOOD, PNR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (13) :4910-4913
[6]   INACTIVATION OF A QUISQUALATE-SENSITIVE GLUTAMATE RECEPTOR BY PHOTOSENSITIVE ANALOGS OF PHILANTHOTOXIN [J].
GOODNOW, RA ;
NAKANISHI, K ;
SUDAN, HL ;
USHERWOOD, PNR .
NEUROSCIENCE LETTERS, 1991, 125 (01) :62-64
[7]  
GRISHIN EV, 1986, BIOORG KHIM+, V12, P1121
[8]  
HERLITZE S, 1993, IN PRESS NEURON
[9]   IDENTIFICATION OF A SITE IN GLUTAMATE RECEPTOR SUBUNITS THAT CONTROLS CALCIUM PERMEABILITY [J].
HUME, RI ;
DINGLEDINE, R ;
HEINEMANN, SF .
SCIENCE, 1991, 253 (5023) :1028-1031
[10]   SPIDER TOXINS AS TOOLS FOR DISSECTING ELEMENTS OF EXCITATORY AMINO-ACID TRANSMISSION [J].
JACKSON, H ;
USHERWOOD, PNR .
TRENDS IN NEUROSCIENCES, 1988, 11 (06) :278-283