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评估显色测定法中产物抑制的影响。

Assessing the impact of product inhibition in a chromogenic assay.

机构信息

Department of Applied Mathematics, University of California, Merced, 5200 North Lake Road, Merced, CA, 95340, USA.

Hematology/Oncology, 8202B Mary Ellen Jones Building, Campus Box 7035, Chapel Hill, NC, 27599-7035, USA.

出版信息

Anal Biochem. 2019 Sep 1;580:62-71. doi: 10.1016/j.ab.2019.05.001. Epub 2019 May 12.

Abstract

Chromogenic substrates (CS) are synthetic substrates used to monitor the activity of a target enzyme. It has been reported that some CSs display competitive product inhibition with their target enzyme. Thus, in assays where enzyme activity is continuously monitored over long periods of time, the product inhibition may significantly interfere with the reactions being monitored. Despite this knowledge, it is rare for CSs to be directly incorporated into mathematical models that simulate these assays. This devalues the predictive power of the models. In this study, we examined the interactions between a single enzyme, coagulation factor Xa, and its chromogenic substrate. We developed, and experimentally validated, a mathematical model of a chromogenic assay for factor Xa that explicitly included product inhibition from the CS. We employed Bayesian inference, in the form of Markov-Chain Monte Carlo, to estimate the strength of the product inhibition and other sources of uncertainty such as pipetting error and kinetic rate constants. Our model, together with carefully calibrated biochemistry experiments, allowed for full characterization of the strength and impact of product inhibition in the assay. The effect of CS product inhibition in more complex reaction mixtures was further explored using mathematical models.

摘要

显色底物(CS)是用于监测靶酶活性的合成底物。据报道,一些 CS 对其靶酶表现出竞争性产物抑制。因此,在长时间连续监测酶活性的测定中,产物抑制可能会严重干扰正在监测的反应。尽管有此认识,但将 CS 直接纳入模拟这些测定的数学模型的情况很少见。这降低了模型的预测能力。在这项研究中,我们研究了单个酶凝血因子 Xa 与其显色底物之间的相互作用。我们开发并通过实验验证了一种因子 Xa 显色测定的数学模型,该模型明确包括了 CS 的产物抑制。我们采用贝叶斯推断(以马尔可夫链蒙特卡罗的形式)来估计产物抑制的强度以及其他来源的不确定性,例如移液误差和动力学速率常数。我们的模型与精心校准的生化实验一起,可充分表征测定中产物抑制的强度和影响。使用数学模型进一步探讨了 CS 产物抑制在更复杂的反应混合物中的影响。

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