首页> 外文期刊>The biochemical journal >Characterization of human pre-elafin mutants: full antipeptidase activity is essential to preserve lung tissue integrity in experimental emphysema
【24h】

Characterization of human pre-elafin mutants: full antipeptidase activity is essential to preserve lung tissue integrity in experimental emphysema

机译:人类前弹性蛋白突变体的表征:完整的抗肽酶活性对于在实验性肺气肿中保持肺组织完整性至关重要

获取原文
           

摘要

pPre-elafin is a tight-binding inhibitor of neutrophil elastase and myeloblastin; two enzymes thought to contribute to tissue damage in lung emphysema. Previous studies have established that pre-elafin is also an effective anti-inflammatory molecule. However, it is not clear whether both functions are linked to the antipeptidase activity of pre-elafin. As a first step toward elucidating the structure/function relationship of this protein, we describe here the construction and characterization of pre-elafin variants with attenuated antipeptidase potential. In these mutants, the P1′ methionine residue of the inhibitory loop is replaced by either a lysine (pre-elafinsupM25K/sup) or a glycine (pre-elafinsupM25G/sup) residue. Both mutated variants are stable and display biochemical properties undistinguishable from WT (wild-type) pre-elafin. However, compared with WT pre-elafin, their inhibitory constants are increased by one to four orders of magnitude toward neutrophil elastase, myeloblastin and pancreatic elastase, depending on the variants and enzymes tested. As suggested by molecular modelling, this attenuated inhibitory potential correlates with decreased van der Waals interactions between the variants and the enzymes S1′ subsite. In elastase-induced experimental emphysema in mice, only WT pre-elafin protected against tissue destruction, as assessed by the relative airspace enlargement measured using lung histopathological sections. Pre-elafin and both mutants prevented transient neutrophil alveolitis. However, even the modestly affected pre-elafinsupM25K/sup mutant, as assayed iin vitro/i with small synthetic substrates, was a poor inhibitor of the neutrophil elastase and myeloblastin elastolytic activity measured with insoluble elastin. We therefore conclude that full antipeptidase activity of pre-elafin is essential to protect against lung tissue lesions in this experimental model./p
机译:Pre-elafin是嗜中性粒细胞弹性蛋白酶和成肌成纤维蛋白的紧密结合抑制剂。两种酶被认为会导致肺气肿的组织损伤。先前的研究已经确定,前弹性蛋白也是一种有效的抗炎分子。但是,尚不清楚这两个功能是否都与前弹性蛋白的抗肽酶活性有关。作为阐明这种蛋白质的结构/功能关系的第一步,我们在这里描述了抗肽酶电位降低的前弹性蛋白变体的构建和表征。在这些突变体中,抑制环的P1'甲硫氨酸残基被赖氨酸(pre-elafin M25K )或甘氨酸(pre-elafin M25G )残基取代。两种突变的变体都是稳定的,并且显示出与野生型WT(野生型)前弹性蛋白没有区别的生化特性。但是,与WT前弹性蛋白相比,根据测试的变体和酶的不同,它们对中性粒细胞弹性蛋白酶,成纤维细胞生成素和胰腺弹性蛋白酶的抑制常数增加了1-4个数量级。如分子模型所暗示的,这种减弱的抑制潜力与变体和酶S1'亚位点之间的范德华相互作用降低有关。在小鼠的弹性蛋白酶诱导的实验性肺气肿中,只有WT前弹性蛋白可以防止组织破坏,这是通过使用肺组织病理学切片测量的相对空域扩大来评估的。弹性蛋白前体和两个突变体均预防了短暂性中性粒细胞性肺炎。但是,即使使用少量合成底物在体外进行检测,即使受到中等程度影响的pre-elafin M25K 突变体,也对中性粒细胞弹性蛋白酶和成肌成纤维蛋白的弹性降解活性均表现出较弱的抑制性,用不溶性检测弹性蛋白。因此,我们得出结论,在此实验模型中,前弹性蛋白的充分抗肽酶活性对于预防肺组织损伤至关重要。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号