Oliveira Leida Calegário, De Lima Maria Elena, Pimenta Adriano M C, Mansuelle Pascal, Rochat Hervé, Cordeiro Marta N, Richardson Michael, Figueiredo Suely G
Departamento de Fisiologia e Farmacologia, Instituto de Ciencias Biologicas, UFMG Av. Antônio Carlos, 6627-Pampulha Caixa Postal 486-31270-901, Belo Horizonte, MG, Brazil.
Toxicon. 2003 Dec;42(7):793-800. doi: 10.1016/j.toxicon.2003.10.009.
Several pools of neurotoxic peptides obtained from fractionated Phoneutria nigriventer venom induce different toxicological effects. One of them, PhTx4, is highly toxic towards insects and displays only a slight toxicity when injected in mice. Also, this fraction contains a class of peptides that are able to inhibit glutamate uptake in preparations of mammalian central nervous systems (CNS). In this work a new toxin called PnTx4-3 was isolated from the PhTx4 fraction by reverse phase and anion exchange steps using high performance liquid chromatography (HPLC). Edman sequencing of PnTx4-3 revealed that it was a polypeptide of 48 amino acid residues, containing 10 cysteines cross-linked by five disulfide bridges. The molecular mass measured by ES-Q-TOF mass spectrometry was 5199.49+/-0.64 Da, which is very close to the calculated mass from amino acid sequence (5199.99 Da). This toxin induces immediate excitatory effects when injected intrathoracically in house flies and cockroaches. Intracerebroventricular injections of 30 microg of PnTx4-3 in mice resulted in no apparent signs of intoxication. In order to make an orthologous comparison, pharmacological characterisation were carried out in rat brain synaptosomes by using [3H]-L-glutamate, showed that the whole PhTx4 fraction as well as the pure toxins PnTx4-3, Tx4(6-1) and Tx4(5-5) obtained of this fraction, were able to inhibit the glutamate uptake in the micromolar concentration range. PnTx4-3 inhibits the glutamate uptake in a dose dependent manner, with an IC50 of approximately 1 microM. PnTx4-3 is highly homologous to the Tx4(6-1) and Tx4(5-5) toxins previously described from the same fraction.
从巴西游走蛛毒液分级分离得到的几类神经毒性肽会产生不同的毒理学效应。其中一种,即PhTx4,对昆虫具有高毒性,而注射到小鼠体内时仅表现出轻微毒性。此外,该分级部分包含一类能够抑制哺乳动物中枢神经系统(CNS)制剂中谷氨酸摄取的肽。在这项工作中,使用高效液相色谱(HPLC)通过反相和阴离子交换步骤从PhTx4分级部分中分离出一种名为PnTx4 - 3的新毒素。对PnTx4 - 3进行的埃德曼测序表明,它是一种由48个氨基酸残基组成的多肽,含有10个通过五个二硫键交联的半胱氨酸。通过电喷雾四极杆飞行时间质谱(ES - Q - TOF)测量的分子量为5199.49±0.64 Da,这与根据氨基酸序列计算出的质量(5199.99 Da)非常接近。当向家蝇和蟑螂胸腔内注射这种毒素时会引发立即兴奋效应。向小鼠脑室内注射30微克PnTx4 - 3未产生明显的中毒迹象。为了进行直系同源比较,利用[³H] - L - 谷氨酸在大鼠脑突触体中进行了药理学特性分析,结果表明整个PhTx4分级部分以及从该分级部分获得的纯毒素PnTx4 - 3、Tx4(6 - 1)和Tx4(5 - 5),在微摩尔浓度范围内均能够抑制谷氨酸摄取。PnTx4 - 3以剂量依赖方式抑制谷氨酸摄取,IC50约为1微摩尔。PnTx4 - 3与先前从同一分级部分描述的Tx4(6 - 1)和Tx4(5 - 5)毒素高度同源。