Wullschleger Benno, Kuhn-Nentwig Lucia, Tromp Jan, Kämpfer Urs, Schaller Johann, Schürch Stefan, Nentwig Wolfgang
Zoological Institute, University of Bern, Baltzerstrasse 6, CH-3012 Bern, Switzerland.
Proc Natl Acad Sci U S A. 2004 Aug 3;101(31):11251-6. doi: 10.1073/pnas.0402226101. Epub 2004 Jul 22.
The survival of the spider Cupiennius salei depends on its hunting success, which largely relies on its immediately paralyzing multicomponent venom. Here, we report on the isolation and characterization of CSTX-13, a neurotoxic enhancer in the spider venom. De novo elucidation of the disulfide bridge pattern of CSTX-13 and the neurotoxin CSTX-1 by tandem MS revealed an identical arrangement. However, in contrast to CSTX-1, CSTX-13 is a two-chain peptide with two interchain and two intrachain disulfide bridges. Furthermore, the insecticidal activity of CSTX-13 is synergistically increased in the presence of K+ ions as well as of the cytolytic peptide cupiennin 1a. We demonstrated that the weakly neurotoxic CSTX-13 enhances the paralytic activity of the neurotoxin CSTX-1 by 65% when it is administered with the latter at its entirely nontoxic physiological concentration, which is 440 times below its LD50 concentration.
蜘蛛Cupiennius salei的生存取决于其捕猎成功率,这在很大程度上依赖于其能立即麻痹猎物的多组分毒液。在此,我们报告了蜘蛛毒液中一种神经毒性增强剂CSTX-13的分离与特性。通过串联质谱对CSTX-13和神经毒素CSTX-1的二硫键模式进行从头解析,结果显示二者排列相同。然而,与CSTX-1不同,CSTX-13是一种双链肽,具有两条链间二硫键和两条链内二硫键。此外,在钾离子以及溶细胞肽cupiennin 1a存在的情况下,CSTX-13的杀虫活性会协同增强。我们证明,当以完全无毒的生理浓度(比其半数致死浓度低440倍)与神经毒素CSTX-1一起给药时,弱神经毒性的CSTX-13可使CSTX-1的麻痹活性提高65%。