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一种被单克隆抗体识别的蛇毒金属蛋白酶表位的系统发育保守性,该单克隆抗体可中和出血活性。

Phylogenetic conservation of a snake venom metalloproteinase epitope recognized by a monoclonal antibody that neutralizes hemorrhagic activity.

作者信息

Tanjoni Isabelle, Butera Diego, Spencer Patrick J, Takehara Harumi A, Fernandes Irene, Moura-da-Silva Ana Maria

机构信息

Laboratório de Imunopatologia, Instituto Butantan, Av. Vital Brasil, 1500, São Paulo, CEP: 05503-900, SP, Brazil.

出版信息

Toxicon. 2003 Dec;42(7):809-16. doi: 10.1016/j.toxicon.2003.10.011.

Abstract

Snake venom metalloproteinases (SVMPs) are present in large quantities in venoms of viper snakes and also in some elapids. Jararhagin is a representative of a P-III multidomain hemorrhagic SVMP present in Bothrops jararaca venom. It is comprised of a catalytic, a disintegrin-like and a cysteine-rich domain. Seven anti-jararhagin monoclonal antibodies (MAJar 1-7) were produced, of which six reacted with the disintegrin domain. MAJar 3 recognized an epitope present at the C-terminal part of the disintegrin-like domain, and neutralized jararhagin-induced hemorrhage. In this study, we evaluated the reactivity of these monoclonal antibodies with venoms from 27 species of snakes belonging to different families. MAJar 3 recognized most of the hemorrhagic venoms. By ELISA, MAJar 3 reacted strongly with venoms from Viperidae family and weakly with Colubridae and Elapidae venoms. This recognition pattern was due to bands between 50 and 80 kDa, corresponding to P-III SVMPs. This antibody preferentially neutralized the hemorrhage induced by venoms of Bothrops snakes. This fact suggests that the epitope recognized by MAJar 3 is present in other metalloproteinases throughout snake phylogeny. However, slight structural differences in the epitope may result in insufficient affinity for neutralization of biological activities.

摘要

蛇毒金属蛋白酶(SVMPs)大量存在于蝰蛇毒液中,在一些眼镜蛇科蛇类毒液中也有发现。矛头蝮蛇毒金属蛋白酶是存在于巴西矛头蝮蛇毒液中的一种P-III多结构域出血性SVMP的代表。它由一个催化结构域、一个解整合素样结构域和一个富含半胱氨酸的结构域组成。制备了七种抗矛头蝮蛇毒金属蛋白酶单克隆抗体(MAJar 1-7),其中六种与解整合素结构域发生反应。MAJar 3识别解整合素样结构域C末端部分存在的一个表位,并中和了矛头蝮蛇毒金属蛋白酶诱导的出血。在本研究中,我们评估了这些单克隆抗体与来自不同科的27种蛇毒液的反应性。MAJar 3识别了大多数出血性毒液。通过酶联免疫吸附测定(ELISA),MAJar 3与蝰蛇科毒液反应强烈,与游蛇科和眼镜蛇科毒液反应较弱。这种识别模式归因于50至80 kDa之间的条带,对应于P-III SVMPs。该抗体优先中和巴西矛头蝮属蛇毒液诱导的出血。这一事实表明,MAJar 3识别的表位在整个蛇类系统发育中的其他金属蛋白酶中也存在。然而,表位的微小结构差异可能导致对生物活性中和的亲和力不足。

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