The characterization of conotoxins

被引:26
作者
Craig, AG [1 ]
机构
[1] Salk Inst Biol Studies, Clayton Fdn Labs Peptide Biol, La Jolla, CA 92037 USA
来源
JOURNAL OF TOXICOLOGY-TOXIN REVIEWS | 2000年 / 19卷 / 01期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1081/TXR-100100315
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Conotoxins are peptide toxins synthesized by marine cone snails for both prey entrapment and defense. The peptides, when injected into the prey, cause immobilization and death. Cone snails are widely distributed in tropical waters, their prey includes fish, worms and other marine snails. The peptide toxins have very high specificity and selectivity for a variety of neuro receptors and ion channels. This makes the toxins very useful in studies aimed at identifying receptors and their ligands, as well as in drug development studies. Conotoxins are notable at the level of primary amino acid sequence for their high percentage of cysteine residues and other post-translational modifications including hydroxylation of proline, gamma-carboxylation of glutamate, pyroglutamic acid formation, bromination of tryptophan and C-terminal amidation. This review describes traditional and more novel techniques for the characterization of conotoxins. In particular, the identification of the nature and the site of post-translational modifications is emphasized. Among the different techniques used to characterize the conotoxins, the important role played by mass spectrometry is emphasized.
引用
收藏
页码:53 / 93
页数:41
相关论文
共 134 条
[41]   INSITU REDUCTION SUITABLE FOR MATRIX-ASSISTED LASER DESORPTION IONIZATION AND LIQUID SECONDARY IONIZATION USING TRIS(2-CARBOXYETHYL)PHOSPHINE [J].
FISCHER, WH ;
RIVIER, JE ;
CRAIG, AG .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 1993, 7 (03) :225-228
[42]   (HYDROXYPROLINE(9)) LUTEINIZING-HORMONE-RELEASING HORMONE - A NOVEL PEPTIDE IN MAMMALIAN AND FROG HYPOTHALAMUS [J].
GAUTRON, JP ;
PATTOU, E ;
BAUER, K ;
KORDON, C .
NEUROCHEMISTRY INTERNATIONAL, 1991, 18 (02) :221-235
[43]  
GIBBS WW, 1996, SCI AM FEB, P28
[44]   LIQUID SECONDARY-ION MASS-SPECTROMETRY OF PHOSPHORYLATED AND SULFATED PEPTIDES AND PROTEINS [J].
GIBSON, BW ;
COHEN, P .
METHODS IN ENZYMOLOGY, 1990, 193 :480-501
[45]   MATRIX COMPOUNDS FOR FAST ATOM BOMBARDMENT MASS-SPECTROMETRY [J].
GOWER, JL .
BIOMEDICAL MASS SPECTROMETRY, 1985, 12 (05) :191-196
[46]   DISULFIDE STRUCTURES OF HIGHLY BRIDGED PEPTIDES - A NEW STRATEGY FOR ANALYSIS [J].
GRAY, WR .
PROTEIN SCIENCE, 1993, 2 (10) :1732-1748
[47]  
GRAY WR, 1983, J BIOL CHEM, V258, P2247
[48]   CONTOXIN GI - DISULFIDE BRIDGES, SYNTHESIS, AND PREPARATION OF IODINATED DERIVATIVES [J].
GRAY, WR ;
LUQUE, FA ;
GALYEAN, R ;
ATHERTON, E ;
SHEPPARD, RC ;
STONE, BL ;
REYES, A ;
ALFORD, J ;
MCINTOSH, M ;
OLIVERA, BM ;
CRUZ, LJ ;
RIVIER, J .
BIOCHEMISTRY, 1984, 23 (12) :2796-2802
[49]   ECHISTATIN DISULFIDE BRIDGES - SELECTIVE REDUCTION AND LINKAGE ASSIGNMENT [J].
GRAY, WR .
PROTEIN SCIENCE, 1993, 2 (10) :1749-1755
[50]  
GRAY WR, 1981, J BIOL CHEM, V256, P4734