Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, 13, Place Pasteur, 1002 Tunis Belvédère, Tunisia.
Matrix Biol. 2010 Mar;29(2):117-26. doi: 10.1016/j.matbio.2009.09.009. Epub 2009 Oct 4.
Leberagin-C, a new member of the disintegrin-like/cysteine-rich (D/C) family, was purified to homogeneity from the venom of Tunisian snake Macrovipera lebetina transmediterranea. It is a monomeric protein with a molecular mass of 25,787 Da. Its complete sequence of 205 amino acid residues was established by cDNA cloning. The leberagin-C shows many conserved sequences with other known D/C proteins, like the SECD binding sites and a pattern of 28 cysteines. It is the first purified protein from M. lebetina transmediterranea with only two disintegrin-like/cysteine-rich domains. Leberagin-C is able to inhibit platelet aggregation induced by thrombin and arachidonic acid with IC(50) of 40 and 50 nM respectively. It was also able to inhibit the adhesion of melanoma tumour cells on fibrinogen and fibronectin, by interfering with the function of alphavbeta3 and, to a lesser extent, with alphavbeta6 and alpha5beta1 integrins. To our knowledge, leberagin-C is the sole described D/C protein that does not specifically interact with the alpha2beta1 integrin. Structure-activity relationship study of leberagin-C suggested that there are some important amino acid differences with jararhagin, the most studied PIII metalloprotease from Bothrops jararaca, notably around the SECD motif in its disintegrin-like domain. Other regions implicated in leberagin-C specificities could not be excluded.
利贝加因-C,一种新的解整合素样/富含半胱氨酸(D/C)家族成员,从北非毒蛇 Macrovipera lebetina transmediterranea 的毒液中被纯化至均一性。它是一种单体蛋白,分子量为 25787 Da。通过 cDNA 克隆确定了其 205 个氨基酸残基的完整序列。利贝加因-C 与其他已知的 D/C 蛋白具有许多保守序列,如 SECD 结合位点和 28 个半胱氨酸模式。它是从 M. lebetina transmediterranea 中分离得到的具有两个解整合素样/富含半胱氨酸结构域的唯一蛋白质。利贝加因-C 能够抑制凝血酶和花生四烯酸诱导的血小板聚集,IC50 分别为 40 和 50 nM。它还能够通过干扰 alphavbeta3 的功能,以及在较小程度上干扰 alphavbeta6 和 alpha5beta1 整合素的功能,抑制黑素瘤肿瘤细胞在纤维蛋白原和纤维连接蛋白上的黏附。据我们所知,利贝加因-C 是唯一描述的不与 alpha2beta1 整合素特异性相互作用的 D/C 蛋白。利贝加因-C 的结构-活性关系研究表明,它在其解整合素样结构域中的 SECD 基序周围与 jararhagin(来自 Bothrops jararaca 的最研究的 PIII 金属蛋白酶)有一些重要的氨基酸差异。不能排除其他与利贝加因-C 特异性相关的区域。