Costa Tassia R, Menaldo Danilo L, Oliveira Clayton Z, Santos-Filho Norival A, Teixeira Sabrina S, Nomizo Auro, Fuly André L, Monteiro Marta C, de Souza Bibiana M, Palma Mário S, Stábeli Rodrigo G, Sampaio Suely V, Soares Andreimar M
Departamento de Análises Clínicas, Toxicológicas e Bromatológicas, Universidade de São Paulo, FCFRP-USP, Ribeirão Preto, SP, Brazil.
Peptides. 2008 Oct;29(10):1645-56. doi: 10.1016/j.peptides.2008.05.021. Epub 2008 Jun 5.
This paper reports the purification and biochemical/pharmacological characterization of two myotoxic phospholipases A(2) (PLA(2)s) from Bothrops brazili venom, a native snake from Brazil. Both myotoxins (MTX-I and II) were purified by a single chromatographic step on a CM-Sepharose ion-exchange column up to a high purity level, showing M(r) approximately 14,000 for the monomer and 28,000Da for the dimer. The N-terminal and internal peptide amino acid sequences showed similarity with other myotoxic PLA(2)s from snake venoms, MTX-I belonging to Asp49 PLA(2) class, enzymatically active, and MTX-II to Lys49 PLA(2)s, catalytically inactive. Treatment of MTX-I with BPB and EDTA reduced drastically its PLA(2) and anticoagulant activities, corroborating the importance of residue His48 and Ca(2+) ions for the enzymatic catalysis. Both PLA(2)s induced myotoxic activity and dose-time dependent edema similar to other isolated snake venom toxins from Bothrops and Crotalus genus. The results also demonstrated that MTXs and cationic synthetic peptides derived from their 115-129 C-terminal region displayed cytotoxic activity on human T-cell leukemia (JURKAT) lines and microbicidal effects against Escherichia coli, Candida albicans and Leishmania sp. Thus, these PLA(2) proteins and C-terminal synthetic peptides present multifunctional properties that might be of interest in the development of therapeutic strategies against parasites, bacteria and cancer.
本文报道了从巴西本土蛇巴西矛头蝮蛇毒中纯化出的两种肌毒性磷脂酶A2(PLA2)及其生化/药理学特性。两种肌毒素(MTX-I和II)通过在CM-琼脂糖离子交换柱上的单一色谱步骤纯化至高纯度水平,单体的相对分子质量(Mr)约为14,000,二聚体为28,000Da。N端和内部肽段氨基酸序列与其他蛇毒中的肌毒性PLA2相似,MTX-I属于Asp49 PLA2类,具有酶活性,而MTX-II属于Lys49 PLA2,无催化活性。用溴酚蓝(BPB)和乙二胺四乙酸(EDTA)处理MTX-I可显著降低其PLA2和抗凝活性,证实了His48残基和Ca2+离子对酶催化的重要性。这两种PLA2均诱导出与从矛头蝮属和响尾蛇属分离出的其他蛇毒毒素相似的肌毒性活性和剂量-时间依赖性水肿。结果还表明,MTXs及其115-129 C端区域衍生的阳离子合成肽对人T细胞白血病(JURKAT)细胞系具有细胞毒性活性,并对大肠杆菌、白色念珠菌和利什曼原虫具有杀菌作用。因此,这些PLA2蛋白和C端合成肽具有多功能特性,可能在开发针对寄生虫、细菌和癌症的治疗策略方面具有重要意义。