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Peptidomic analysis of blood plasma after in vivo treatment with protease inhibitors--a proof of concept study.

机译:蛋白酶抑制剂体内治疗后血浆的肽段分析-概念研究的证明。

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Native peptides can be regarded as surrogate markers for protease activity in biological samples. Analysis of peptides by peptidomics allows to monitor protease activity in vivo and to describe the influence of protease inhibition. To elucidate the potential of peptides as markers for in vivo protease inhibition we analyzed plasma samples from animals treated with either the indirect FXa inhibitor FONDAPARINUX or the dipeptidylpeptidase IV inhibitor AB192. Signals correlating with the treatment were subsequently identified and assessed with respect to protease-dependent consensus cleavage motifs and occurrence of downstream targets. It could be shown that regulated peptides were either substrates, products or downstream targets of the inhibited protease. The results from the present study demonstrate that the in vivo analysis of peptides by peptidomics has the potential to broaden the knowledge of inhibitor related effects in vivo and that this method may pave the way to develop predictive biomarkers.
机译:天然肽可以被认为是生物样品中蛋白酶活性的替代标记。通过肽组学对肽进行分析可以监测体内的蛋白酶活性并描述蛋白酶抑制的影响。为了阐明肽作为体内蛋白酶抑制标记物的潜力,我们分析了用间接FXa抑制剂FONDAPARINUX或二肽基肽酶IV抑制剂AB192处理过的动物的血浆样品。随后确定和评估与治疗相关的信号,并评估蛋白酶依赖性共有裂解基序和下游靶标的发生。可以表明,调节的肽是被抑制的蛋白酶的底物,产物或下游靶标。本研究的结果表明,通过肽组学对肽进行体内分析有可能拓宽体内抑制剂相关作用的知识,并且该方法可能为开发预测性生物标志物铺平道路。

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