A NEW CONUS PEPTIDE LIGAND FOR CA CHANNEL SUBTYPES

被引:57
|
作者
MONJE, VD
HAACK, JA
NAISBITT, SR
MILJANICH, G
RAMACHANDRAN, J
NASDASDI, L
OLIVERA, BM
HILLYARD, DR
GRAY, WR
机构
[1] UNIV UTAH,DEPT BIOL,SALT LAKE CITY,UT 84112
[2] NEUREX CORP,MENLO PK,CA
[3] UNIV UTAH,DEPT PATHOL,SALT LAKE CITY,UT 84112
关键词
CALCIUM; CALCIUM CHANNEL; OMEGA-CONOTOXIN; CONUS-MAGUS; OMEGA-CONOTOXIN MVIID;
D O I
10.1016/0028-3908(93)90008-Q
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A cDNA clone encoding a new omega-conotoxin was identified from Conus magus. The predicted peptide was chemically synthesized using a novel strategy that efficiently yielded the biologically active disulfide-bonded isomer. This peptide, omega-conotoxin MVIID, targets other voltage-gated calcium channels besides the N-subtype and exhibits greater discrimination against the N-channel subtype than any other omega-conotoxin variant to date. Consequently, omega-conotoxin MVIID may be a particularly useful ligand for calcium channel subtypes that are not of the L- or N-subclasses. Of the eight major sequence variants of omega-conotoxins that have been elucidated, four come from Conus magus venom. We suggest that sequence variants from the same venom may be designed to optimally interact with different molecular variants of calcium channels; such omega-conotoxin sets from a single venom may therefore be useful for helping to identify novel calcium channel subtypes.
引用
收藏
页码:1141 / 1149
页数:9
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