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二肽基肽酶 IV 活性测定方法的比较及其在含有可逆抑制剂的生物样品中的应用。

Method comparison of dipeptidyl peptidase IV activity assays and their application in biological samples containing reversible inhibitors.

机构信息

Laboratory of Medical Biochemistry, University of Antwerp, Antwerp, Belgium.

出版信息

Clin Chim Acta. 2012 Feb 18;413(3-4):456-62. doi: 10.1016/j.cca.2011.10.031. Epub 2011 Nov 7.

Abstract

BACKGROUND

Dipeptidyl peptidase IV (DPPIV, DPP4) is a serine protease that releases N-terminal dipeptides. It is a validated drug target for type 2 diabetes and DPPIV inhibitors are currently evaluated for other therapeutic applications. Various assays are used for DPPIV activity measurements in biological samples. Highly sensitive methods are needed to measure also very low activities in inhibited samples.

METHODS

Here, the three most extensively used substrates to quantify DPPIV activity are compared using in-house methods. A luminescent kit was also included. In addition, one of the in-house fluorometric assays was elaborated for use in biological samples containing reversible DPPIV inhibitors to estimate residual DPPIV activity which is usually underestimated due to sample dilution.

RESULTS

The in-house methods showed a good precision, linearity and specificity. Both fluorometric substrates had a 10-fold higher sensitivity compared to the colorimetric assay. The luminescent kit was found to be the most sensitive.

CONCLUSIONS

All three in-house methods can be used to measure DPPIV activity in non-inhibited biological samples. The more sensitive fluorometric assays are recommended when sample volumes are limited or when using inhibited samples. The elaborated fluorometric method can be used to estimate the residual in vivo DPPIV activity in inhibitor treated subjects.

摘要

背景

二肽基肽酶 IV(DPPIV,DPP4)是一种丝氨酸蛋白酶,可释放 N 端二肽。它是 2 型糖尿病的有效药物靶点,目前正在评估 DPPIV 抑制剂在其他治疗应用中的作用。各种测定法用于测量生物样品中的 DPPIV 活性。需要高度灵敏的方法来测量抑制样品中的非常低的活性。

方法

本文使用内部方法比较了三种最广泛用于定量 DPPIV 活性的底物。还包括一个发光试剂盒。此外,还对一种内部荧光测定法进行了阐述,用于含有可逆 DPPIV 抑制剂的生物样品中,以估计残留的 DPPIV 活性,由于样品稀释,通常会低估该活性。

结果

内部方法显示出良好的精密度、线性和特异性。两种荧光底物的灵敏度比比色测定法高 10 倍。发现发光试剂盒最灵敏。

结论

所有三种内部方法都可用于测量非抑制性生物样品中的 DPPIV 活性。当样品体积有限或使用抑制样品时,建议使用更灵敏的荧光测定法。阐述的荧光测定法可用于估计抑制剂处理的受试者体内残留的 DPPIV 活性。

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