The Spasmodic Peptide Defines a New Conotoxin Superfamily
We purified and characterized a peptide from the venom of Conus textile that makes normal mice assume the phenotype of a well-known mutant, the spasmodic mouse. This “spasmodic” peptide has 27 amino acids, including two γ-carboxyglutamate (Gla) residues. A cDNA clone encoding the precursor for the p...
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Veröffentlicht in: | Biochemistry (Easton) 2000-02, Vol.39 (7), p.1583-1588 |
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Sprache: | eng |
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Zusammenfassung: | We purified and characterized a peptide from the venom of Conus textile that makes normal mice assume the phenotype of a well-known mutant, the spasmodic mouse. This “spasmodic” peptide has 27 amino acids, including two γ-carboxyglutamate (Gla) residues. A cDNA clone encoding the precursor for the peptide was identified; a γ-carboxylation recognition signal sequence (γ-CRS) is present in the −1 → −20 region of the peptide precursor. Both the γ-CRS and the position of the Gla residues in the mature toxin are notably different from other Gla-containing conopeptides. The spasmodic peptide has a novel disulfide framework and distinct signal sequence which together define a new P-superfamily of conopeptides. A cDNA encoding another member of the P-superfamily was identified from a different species, Conus gloriamaris. |
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ISSN: | 0006-2960 1520-4995 |
DOI: | 10.1021/bi9923712 |