首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Recombinant alpha 1-antitrypsin Pittsburgh (Met 358----Arg) is a potent inhibitor of plasma kallikrein and activated factor XII fragment.
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Recombinant alpha 1-antitrypsin Pittsburgh (Met 358----Arg) is a potent inhibitor of plasma kallikrein and activated factor XII fragment.

机译:重组α1-抗胰蛋白酶匹兹堡(Met 358 ---- Arg)是血浆激肽释放酶和活化因子XII片段的有效抑制剂。

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摘要

In normal plasma, the serine protease inhibitor alpha 1-antitrypsin (alpha 1-AT) plays little or no role in the control of plasma kallikrein or activated Factor XII fragment (Factor XIIf), this function being performed by Cl-inhibitor. Recently, an alpha 1-AT variant was described with a Met----Arg mutation at the reactive center P1 residue (position 358) which altered the specificity of inhibition from the Met- or Val-specific protease neutrophil elastase to thrombin, an Arg-specific protease. We have now examined the inhibition of plasma kallikrein and Factor XIIf, both Arg-specific enzymes, with recombinant alpha 1-AT(Met358----Arg) produced by an Escherichia coli strain carrying a mutated human alpha 1-AT gene. The engineered protein was a very efficient inhibitor of both enzymes. It was more effective than Cl-inhibitor by a factor of 4.1 for kallikrein and 11.5 for Factor XIIf. These results suggest that recombinant alpha 1-AT(Met358----Arg) has therapeutic potential for disease states where activation of the plasma kinin-forming system is observed, for example in hereditary angioedema or septic shock.
机译:在正常血浆中,丝氨酸蛋白酶抑制剂α1-抗胰蛋白酶(α1-AT)在血浆激肽释放酶或活化的因子XII片段(因子XIIf)的控制中几乎没有或没有任何作用,该功能由Cl抑制剂执行。最近,描述了一种在反应中心P1残基(位置358)具有Met ---- Arg突变的alpha 1-AT变体,该突变改变了Met或Val特异性蛋白酶中性粒细胞弹性蛋白酶对凝血酶的抑制特异性。 Arg特异性蛋白酶。现在,我们已经研究了由携带突变的人α1-AT基因的大肠杆菌菌株产生的重组α1-AT(Met358-Arg)对血浆激肽释放酶和因子XIIf(这两种Arg特异性酶)的抑制作用。工程蛋白是两种酶的非常有效的抑制剂。它对激肽释放酶的作用比Cl抑制剂高4.1倍,对因子XIIf则高11.5倍。这些结果表明,重组α1-AT(Met358 ---- Arg)具有治疗潜力,可用于观察到血浆激肽形成系统活化的疾病状态,例如在遗传性血管性水肿或败血性休克中。

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