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Validation of Fractal-Like Kinetic Models by Time-Resolved Binding Kinetics of Dansylamide and Carbonic Anhydrase in Crowded Media

机译:在拥挤的介质中通过时间分辨的丹磺酰胺和碳酸酐酶的结合动力学验证分形动力学模型

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摘要

Kinetic studies of biochemical reactions are typically carried out in a dilute solution that rarely contains anything more than reactants, products, and buffers. In such studies, mass-action-based kinetic models are used to analyze the progress curves. However, intracellular compartments are crowded by macromolecules. Therefore, we investigated the adequacy of the proposed generalizations of the mass-action model, which are meant to describe reactions in crowded media. To validate these models, we measured time-resolved kinetics for dansylamide binding to carbonic anhydrase in solutions crowded with polyethylene glycol and Ficoll. The measured progress curves clearly show the effects of crowding. The fractal-like model proposed by Savageau was used to fit these curves. In this model, the association rate coefficient ka allometrically depends on concentrations of reactants. We also considered the fractal kinetic model proposed by Schnell and Turner, in which ka depends on time according to a Zipf-Mandelbrot distribution, and some generalizations of these models. We found that the generalization of the mass-action model, in which association and dissociation rate coefficients are concentration-dependent, represents the preferred model. Other models based on time-dependent rate coefficients were inadequate or not preferred by model selection criteria.
机译:生化反应的动力学研究通常是在稀溶液中进行的,稀溶液中几乎不包含反应物,产物和缓冲液。在此类研究中,基于质量作用的动力学模型用于分析进度曲线。然而,细胞内区室被大分子拥挤。因此,我们调查了所提出的质量模型的一般性,以描述拥挤介质中的反应。为了验证这些模型,我们测量了在充满聚乙二醇和Ficoll的溶液中丹磺酰胺与碳酸酐酶结合的时间分辨动力学。测得的进度曲线清楚地显示了拥挤的影响。 Savageau提出的分形模型用于拟合这些曲线。在该模型中,缔合速率系数ka异乎寻常地取决于反应物的浓度。我们还考虑了Schnell和Turner提出的分形动力学模型,其中ka根据Zipf-Mandelbrot分布取决于时间,并对这些模型进行了一些推广。我们发现质量运动模型的一般化(其中缔合和解离速率系数是浓度依赖性的)代表了首选模型。基于时间依赖性速率系数的其他模型不足或不被模型选择标准所偏爱。

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