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小血清蛋白-1改变了诱导凋亡的金属蛋白酶 HV1 对眼镜蛇(Trimeresurus flavoviridis)金属蛋白酶抑制剂的敏感性。

Small serum protein-1 changes the susceptibility of an apoptosis-inducing metalloproteinase HV1 to a metalloproteinase inhibitor in habu snake (Trimeresurus flavoviridis).

机构信息

Department of Chemistry, Faculty of Science, Fukuoka University, Fukuoka 814-0180, Japan.

出版信息

J Biochem. 2013 Jan;153(1):121-9. doi: 10.1093/jb/mvs127. Epub 2012 Oct 25.

Abstract

Viperidae snakes containing various venomous proteins also have several anti-toxic proteins in their sera. However, the physiological function of serum protein has been elucidated incompletely. Small serum protein (SSP)-1 is a major component of the SSPs isolated from the serum of a Japanese viper, the habu snake (Trimeresurus flavoviridis). It exists in the blood as a binary complex with habu serum factor (HSF), a snake venom metalloproteinase inhibitor. Affinity chromatography of the venom on an SSP-1-immobilized column identified HV1, an apoptosis-inducing metalloproteinase, as the target protein of SSP-1. Biacore measurements revealed that SSP-1 was bound to HV1 with a dissociation constant of 8.2 × 10⁻⁸ M. However, SSP-1 did not inhibit the peptidase activity of HV1. Although HSF alone showed no inhibitory activity or binding affinity to HV1, the SSP-1-HSF binary complex bound to HV1 formed a ternary complex that non-competitively inhibited the peptidase activity of HV1 with a inhibition constant of 5.1 ± 1.3 × 10⁻⁹ M. The SSP-1-HSF complex also effectively suppressed the apoptosis of vascular endothelial cells and caspase 3 activation induced by HV1. Thus, SSP-1 is a unique protein that non-covalently attaches to HV1 and changes its susceptibility to HSF.

摘要

蝰科蛇含有各种毒性蛋白,其血清中也含有几种抗毒蛋白。然而,血清蛋白的生理功能尚未完全阐明。小血清蛋白 (SSP)-1 是从日本毒蛇(虎蛇,Trimeresurus flavoviridis)血清中分离出的 SSPs 的主要成分。它以与蛇毒金属蛋白酶抑制剂虎蛇血清因子(HSF)形成二元复合物的形式存在于血液中。将毒液在 SSP-1 固定化柱上进行亲和层析,鉴定出 HV1,一种诱导细胞凋亡的金属蛋白酶,为 SSP-1 的靶蛋白。Biacore 测量显示 SSP-1 与 HV1 的解离常数为 8.2×10⁻⁸ M。然而,SSP-1 并没有抑制 HV1 的肽酶活性。尽管 HSF 本身对 HV1 没有抑制活性或结合亲和力,但 SSP-1-HSF 二元复合物与 HV1 结合形成三元复合物,以非竞争性方式抑制 HV1 的肽酶活性,抑制常数为 5.1±1.3×10⁻⁹ M。SSP-1-HSF 复合物还能有效抑制 HV1 诱导的血管内皮细胞凋亡和 caspase 3 激活。因此,SSP-1 是一种独特的蛋白,它与 HV1 非共价结合,并改变其对 HSF 的敏感性。

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