Zamora-Bustillos Roberto, Aguilar Manuel B, Falcón Andrés, Heimer de la Cotera Edgar P
Laboratorio de Neurofarmacología Marina, Departamento de Neurobiología Celular y Molecular, Instituto de Neurobiología, Universidad Nacional Autónoma de México, Campus Juriquilla, Querétaro 76230, Mexico.
Peptides. 2009 Aug;30(8):1396-404. doi: 10.1016/j.peptides.2009.05.003. Epub 2009 May 15.
cDNA was prepared from the venom duct of a single Conus spurius specimen collected near the coast of Campeche, Mexico. From it, PCR products were generated, sequenced, and predicted to encode eight distinct precursors of T-1-conotoxins. These precursors contain five different mature toxins, of which four are novel and one (sr5a) has been previously purified and characterized from the venom of this species. Three of the novel toxins are very similar to sr5a: two have one amino acid substitution at position 8, whereas the other is predicted to have one additional residue at the C-terminus; the fourth toxin has five amino acid substitutions and is predicted to have two additional residues at the C-terminus. In general, the precursors include a 22-residue signal peptide, a 24-residue "pro" region, and a 13- to 16-residue mature toxin region; however, the C-termini of two mature toxin regions are predicted to be altered by post-translational processing. Three precursors lack, in the same positions, 15 amino acid residues included in the "pre" (one residue) and "pro" (14 residues) regions, which suggests the existence of an exon encoding the last signal peptide residue and the first 14 residues of the "pro" region. Phylogenetic analysis indicates that the T-1-conotoxin precursors and mature toxins of C. spurius are more similar to certain precursors and toxins from molluscivorous Conus species than to any precursors and toxins from vermivorous cones. The results reported here will be useful for synthesizing the novel toxins in order to identify their molecular targets.
从墨西哥坎佩切海岸附近采集的单个斯氏芋螺标本的毒管中制备了互补DNA(cDNA)。由此产生了聚合酶链式反应(PCR)产物,进行了测序,并预测其编码8种不同的T-1芋螺毒素前体。这些前体包含5种不同的成熟毒素,其中4种是新发现的,1种(sr5a)先前已从该物种的毒液中纯化并鉴定。3种新毒素与sr5a非常相似:2种在第8位有一个氨基酸取代,而另一种预计在C端有一个额外的残基;第4种毒素有5个氨基酸取代,预计在C端有两个额外的残基。一般来说,前体包括一个22个残基的信号肽、一个24个残基的“原”区域和一个13至16个残基的成熟毒素区域;然而,两个成熟毒素区域的C端预计会通过翻译后加工而改变。3种前体在相同位置缺少“前”(1个残基)和“原”(14个残基)区域中的15个氨基酸残基,这表明存在一个编码最后一个信号肽残基和“原”区域前14个残基的外显子。系统发育分析表明,斯氏芋螺的T-1芋螺毒素前体和成熟毒素与食软体动物芋螺物种的某些前体和毒素比与食蠕虫芋螺的任何前体和毒素更相似。此处报告的结果将有助于合成新毒素以确定其分子靶点。