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Kinetics of Single-Enzyme Reactions on Vesicles: Role of Substrate Aggregation

机译:囊泡上的单酶反应动力学:底物聚集的作用

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Enzymatic reactions occurring in vivo on lipid membranes can be influenced by various factors including macromolecular crowding in general and substrate aggregation in particular. In academic studies, the role of these factors can experimentally be clarified by tracking single-enzyme kinetics occurring on individual lipid vesicles. To extend the conceptual basis for such experiments, we analyze herein the corresponding kinetics mathematically with emphasis on the role of substrate aggregation. In general, the aggregation may occur on different length scales. Small aggregates may e.g. contain a few proteins or peptides while large aggregates may be mesoscopic as in the case of lipid domains which can be formed in the membranes composed of different lipids. We present a kinetic model describing comprehensively the effect of aggregation of the former type on the dependence of the reaction rate on substrate membrane concentration. The results obtained with physically reasonable parameters indicate that the aggregation-related deviations from the conventional Michaelis-Menten kinetics may be appreciable.
机译:体内在脂质膜上发生的酶促反应会受到多种因素的影响,这些因素通常包括大分子拥挤,尤其是底物聚集。在学术研究中,这些因子的作用可以通过追踪单个脂质囊泡上发生的单酶动力学来实验确定。为了扩展此类实验的概念基础,我们在此处通过数学方法分析相应的动力学,重点是底物聚集的作用。通常,聚集可以在不同的长度尺度上发生。小聚集体例如包含一些蛋白质或肽,而大的聚集体可能是介观的,例如在可以由不同脂质组成的膜中形成的脂质结构域的情况下。我们提供了一个动力学模型,全面描述了前一种类型的聚集对反应速率对底物膜浓度的依赖性的影响。使用物理上合理的参数获得的结果表明,与聚合相关的偏离与常规Michaelis-Menten动力学可能是可观的。

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