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从优雅海葵(Anthopleura elegantissima)中分离并鉴定出五种具有神经毒性和心脏毒性的多肽。

Isolation and characterisation of five neurotoxic and cardiotoxic polypeptides from the sea anemone Anthopleura elegantissima.

作者信息

Bruhn T, Schaller C, Schulze C, Sanchez-Rodriguez J, Dannmeier C, Ravens U, Heubach J F, Eckhardt K, Schmidtmayer J, Schmidt H, Aneiros A, Wachter E, Béress L

机构信息

Institute of Toxicology, Medical Faculty Christian-Albrechts-University, Brunswikerstrasse 10, 24105, Kiel, Germany.

出版信息

Toxicon. 2001 May;39(5):693-702. doi: 10.1016/s0041-0101(00)00199-9.

Abstract

Five toxins (APE 1 to APE 5) of the sea anemone species Anthopleura elegantissima (Brandt) have been isolated from a toxic by-product fraction of its concentrated crude watery-methanolic extract, prepared previously for the isolation of a neuropeptide (the head-activator) by Schaller and Bodenmüller (Proc. Natl. Acad. Sci. USA 78 (1981) 7000) from 200kg sea anemones. Toxin purification was performed by desalting of the starting material by dialysis (MWCO 3500) against distilled water, anion exchange chromatography on QAE-Sephadex A25 at pH 8, twice gel filtration on Sephadex G50 m, repeated chromatography on QAE-Sephadex at pH 10 and chromatography on the cation exchanger Fractogel EMD SO(3)(-)-650 M.Final purification of the toxins was achieved by HPLC on MN SP 250/10 Nucleosil 500-5 C(18) PPN and MN SP 250/21 Nucleosil 300-7 C(18). Each toxin was composed of at least two isotoxins of which APE 1-1, APE 1-2, APE 2-1, APE 2-2 and APE 5-3 were isolated in preparative scale. With exception of APE 5-3 the sequences of the isotoxins have been elucidated. They resemble the 47 residue type-I long polypeptide toxins native to Anemonia sulcata (Pennant). All isotoxins paralyse the shore crab (Carcinus maenas) by tetanic contractions after i.m. application. The toxins modify current passing through the fast Na(+) channel in neuroblastoma cells, leading to delayed and incomplete inactivation. APE 1-1, APE 2-1 and APE 5-3 produce a positive inotropic effect in mammalian heart muscle, although they differ in potency. The order of potency is APE 2-1>APE 1-1>APE 5-3 (i.e. threshold concentrations are 1, 10 and 300nM, respectively). In addition, they enhance the spontaneous beating frequency in isolated right atria (guinea pig). The most potent cardiotoxic isotoxin is APE 2-1, its sequence is identical with that of AP-C, a toxin isolated and characterised previously by Norton et al. (Drugs and Foods from the Sea, 1978, University of Oklahoma Press, p. 37-50).LD50 APE 2-1:1 micro g/kg b.w. C. maenas (i.m.). LD50 APE 1-1:10 microg/kg b.w. C. maenas (i. m.). LD50 APE 5-3:50 microg/kg b.w. C. maenas (i.m.).

摘要

从海葵华丽海葵(布兰特)的浓缩粗水 - 甲醇提取物的有毒副产物部分中分离出了五种毒素(APE 1至APE 5)。该提取物先前由沙勒和博登米勒(《美国国家科学院院刊》78 (1981) 7000)从200千克海葵中制备,用于分离一种神经肽(头部激活剂)。毒素的纯化过程包括:通过对蒸馏水进行透析(截留分子量3500)对起始材料进行脱盐,在pH 8的QAE - 葡聚糖A25上进行阴离子交换色谱,在Sephadex G50 m上进行两次凝胶过滤,在pH 10的QAE - 葡聚糖上重复色谱,以及在阳离子交换剂Fractogel EMD SO(3)(-) - 650 M上进行色谱。毒素的最终纯化通过在MN SP 250/10 Nucleosil 500 - 5 C(18) PPN和MN SP 250/21 Nucleosil 300 - 7 C(18)上进行高效液相色谱实现。每种毒素至少由两种同毒素组成,其中APE 1 - 1、APE 1 - 2、APE 2 - 1、APE 2 - 2和APE 5 - 3以制备规模分离出来。除了APE 5 - 3之外,同毒素的序列已经阐明。它们类似于来自沟海葵(彭南特)的47个残基的I型长多肽毒素。所有同毒素在肌肉注射后通过强直性收缩使岸蟹(欧洲绿蟹)麻痹。这些毒素改变通过神经母细胞瘤细胞中快速钠通道的电流,导致延迟和不完全失活。APE 1 - 1、APE 2 - 1和APE 5 - 3在哺乳动物心肌中产生正性肌力作用,尽管它们的效力不同。效力顺序为APE 2 - 1>APE 1 - 1>APE 5 - 3(即阈值浓度分别为1、10和300 nM)。此外,它们增加离体右心房(豚鼠)的自发搏动频率。最具心脏毒性的同毒素是APE 2 - 1,其序列与先前由诺顿等人分离和表征的毒素AP - C相同(《来自海洋的药物和食物》,1978年,俄克拉荷马大学出版社,第37 - 50页)。APE 2 - 1对欧洲绿蟹的半数致死量:1微克/千克体重(肌肉注射)。APE 1 - 1对欧洲绿蟹的半数致死量:10微克/千克体重(肌肉注射)。APE 5 - ③对欧洲绿蟹的半数致死量:50微克/千克体重(肌肉注射)。

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