Najib J, Letailleur T, Gesquière J C, Tartar A
Faculté des Sciences Pharmaceutiques et Biologiques, CNRS URA 1309, France.
J Pept Sci. 1996 Sep-Oct;2(5):309-17. doi: 10.1002/psc.57.
omega-Agatoxin IVA, isolated from the venom of funnel web spider Agelenopsis aperta, blocks potently and selectively P-type calcium channels. This toxin, composed of 48 amino acids and containing 8 cysteine residues, was synthesized by the solid-phase procedure. The Cys residues were protected by acetamidomethyl (Acm) groups which were removed by mercuric acetate. During treatment with mercuric acetate, a by-product was detected, involving modification of tryptophan residues by the Acm groups. This side reaction can be completely prevented by addition of an excess of tryptophan in the reaction medium during Acm deprotection. The resulting peptide was submitted to an oxidative refolding, in different conditions, in order to determine the most favourable protocol. After formation of the four disulphide bonds, the toxin was purified by successive preparative HPLC, on two different supports, and fully characterized by analytical HPLC, capillary electrophoresis, amino acid analysis, mass spectrometry and Edman degradation. It was found to block the P-type calcium channel with a similar biological potency as described for the natural product.
ω-阿加毒素IVA是从漏斗网蜘蛛(Agelenopsis aperta)的毒液中分离出来的,它能有效且选择性地阻断P型钙通道。这种由48个氨基酸组成且含有8个半胱氨酸残基的毒素是通过固相法合成的。半胱氨酸残基由乙酰氨基甲基(Acm)基团保护,该基团通过醋酸汞去除。在用醋酸汞处理过程中,检测到一种副产物,涉及Acm基团对色氨酸残基的修饰。在Acm脱保护过程中,通过在反应介质中加入过量的色氨酸可以完全防止这种副反应。将所得肽在不同条件下进行氧化重折叠,以确定最有利的方案。形成四个二硫键后,通过在两种不同载体上连续进行制备型高效液相色谱法对毒素进行纯化,并通过分析型高效液相色谱法、毛细管电泳、氨基酸分析、质谱和埃德曼降解对其进行全面表征。结果发现它阻断P型钙通道的生物活性与天然产物相似。