Hermogenes Ana L, Richardson Michael, Magalhaes Arinos, Yarleque Armando, Rodriguez Edith, Sanchez Eladio F
Research and Development Center, Ezequiel Dias Fundation, 30510-010 Belo Horizonte, MG, Brazil.
Toxicon. 2006 Mar 15;47(4):490-4. doi: 10.1016/j.toxicon.2005.12.009. Epub 2006 Feb 3.
Lachesis venom plasminogen activator (LV-PA) is a 33-kDa serine proteinase isolated from bushmaster (Lachesis muta muta) snake venom, which activates the fibrinolytic system in vitro. This study has examined the effect of the plasma proteinase inhibitor alpha2-macroglobulin (alpha2-M) towards LV-PA and compares it with the effect on tissue type plasminogen activator (t-PA). The proteolytic activity of LV-PA alone or previously incubated with human plasminogen (Plg) on the large molecular mass protein substrates, dimethylcasein (DMC) and fibrinogen (Fg) was completely inhibited by human alpha2-M. However, the synthetic peptides Tos-Gly-Pro-Lys-pNA and H-D-Pro-Phe-Arg-pNA (S-2302) were hydrolyzed with almost no reduction in rate. At pH 7.4 and 37 degrees C the proteinase (0.15 microM over 15 min) interacted with alpha2-M, and each mole of alpha2-M bound 2 mol of enzyme. Sodium dodecyl sulfate gel electrophoresis of reduced samples showed that the interaction of alpha2-M with either LV-PA or t-PA preincubated with Plg resulted in the formation of approximately 90 kDa fragments and high molecular mass complexes (Mr 180 kDa), generated by the incubation mixture (LV-PA or t-PA) and Plg. The data suggest that LV-PA is a direct-type PA and its fibrinolytic effect can be reduced by alpha2-M in vivo.
矛头蝮蛇毒纤溶酶原激活剂(LV-PA)是一种从巨蝮蛇(Lachesis muta muta)蛇毒中分离出的33 kDa丝氨酸蛋白酶,它能在体外激活纤溶系统。本研究检测了血浆蛋白酶抑制剂α2-巨球蛋白(α2-M)对LV-PA的作用,并将其与对组织型纤溶酶原激活剂(t-PA)的作用进行比较。单独的LV-PA或预先与人纤溶酶原(Plg)孵育后的LV-PA对大分子质量蛋白质底物二甲基酪蛋白(DMC)和纤维蛋白原(Fg)的蛋白水解活性被人α2-M完全抑制。然而,合成肽甲苯磺酰甘氨酰脯氨酰赖氨酸对硝基苯胺和H-D-脯氨酰苯丙氨酰精氨酸对硝基苯胺(S-2302)被水解,且速率几乎没有降低。在pH 7.4和37℃条件下,蛋白酶(15分钟内0.15μM)与α2-M相互作用,每摩尔α2-M结合2摩尔酶。还原样品的十二烷基硫酸钠凝胶电泳显示,α2-M与预先与Plg孵育的LV-PA或t-PA相互作用导致形成约90 kDa的片段和高分子质量复合物(Mr 180 kDa),这些是由孵育混合物(LV-PA或t-PA)和Plg产生的。数据表明LV-PA是一种直接型PA,其纤溶作用在体内可被α2-M降低。