TY - JOUR
T1 - Identification of three subunits of the high affinity ω-conotoxin MVIIC-sensitive Ca 2 + channel
AU - Liu, Hongyan
AU - De Waard, Michel
AU - Scott, Victoria E.S.
AU - Gurnett, Christina A.
AU - Lennon, Vanda A.
AU - Campbell, Kevin P.
PY - 1996
Y1 - 1996
N2 - N-, P- and Q-type voltage-dependent Ca2+ channels control neurotransmitter release in the nervous system and are blocked by ω-conotoxin MVIIC. In this study, both a high affinity and a low affinity binding site for ω-conotoxin MVIIC were detected in rabbit brain. The low affinity binding site is shown to be present on the N-type Ca2+ channel. Using optimized conditions for specific labeling of the high affinity ω-conotoxin MVIIC receptor and a panel of subunit specific antibodies, the molecular structure of the high affinity receptor was investigated. We demonstrate for the first time that this receptor is composed of at least α1A, α2δ, and any one of the four brain β subunits. Such association of different β subunits with α1A and α2δ components may produce Ca2+ channels with distinct functional properties, such as P- and Q-type.
AB - N-, P- and Q-type voltage-dependent Ca2+ channels control neurotransmitter release in the nervous system and are blocked by ω-conotoxin MVIIC. In this study, both a high affinity and a low affinity binding site for ω-conotoxin MVIIC were detected in rabbit brain. The low affinity binding site is shown to be present on the N-type Ca2+ channel. Using optimized conditions for specific labeling of the high affinity ω-conotoxin MVIIC receptor and a panel of subunit specific antibodies, the molecular structure of the high affinity receptor was investigated. We demonstrate for the first time that this receptor is composed of at least α1A, α2δ, and any one of the four brain β subunits. Such association of different β subunits with α1A and α2δ components may produce Ca2+ channels with distinct functional properties, such as P- and Q-type.
UR - http://www.scopus.com/inward/record.url?scp=0029933658&partnerID=8YFLogxK
U2 - 10.1074/jbc.271.23.13804
DO - 10.1074/jbc.271.23.13804
M3 - Article
C2 - 8662888
AN - SCOPUS:0029933658
SN - 0021-9258
VL - 271
SP - 13804
EP - 13810
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 23
ER -