Colocalization and Sequential Enzyme Activity in Aqueous Biphasic Systems: Experiments and Modeling

被引:47
作者
Davis, Bradley W. [1 ]
Aumiller, William M., Jr. [1 ]
Hashemian, Negar [2 ]
An, Songon [1 ]
Armaou, Antonios [2 ]
Keating, Christine D. [1 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
PHASE-SEPARATION; HORSERADISH-PEROXIDASE; PARTITION BEHAVIOR; IMP CYCLOHYDROLASE; KINETIC-ANALYSIS; 2-PHASE SYSTEMS; ADENYLOSUCCINATE; PURIFICATION; EXPRESSION; COMPLEXES;
D O I
10.1016/j.bpj.2015.09.020
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Subcellular compartmentalization of biomolecules and their reactions is common in biology and provides a general strategy for improving and/or controlling kinetics in metabolic pathways that contain multiple sequential enzymes. Enzymes can be colocalized in multiprotein complexes, on scaffolds or inside subcellular organelles. Liquid organelles formed by intracellular phase coexistence could provide an additional means of sequential enzyme colocalization. Here we use experiment and computation to explore the kinetic consequences of sequential enzyme compartmentalization into model liquid organelles in a crowded polymer solution. Two proteins of the de novo purine biosynthesis pathway, ASL (adenylosuccinate lyase, Step 8) and ATIC (5-aminoimidazole-4-carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase, Steps 9 and 10), were studied in a polyethylene glycol/dextran aqueous two-phase system. Dextran-rich phase droplets served as model liquid compartments for enzyme colocalization. In this system, which lacks any specific binding interactions between the phase-forming polymers and the enzymes, we did not observe significant rate enhancements from colocalization for the overall reaction under our experimental conditions. The experimental results were used to adapt a mathematical model to quantitatively describe the kinetics. The mathematical model was then used to explore additional, experimentally inaccessible conditions to predict when increased local concentrations of enzymes and substrates can (or cannot) be expected to yield increased rates of product formation. Our findings indicate that colocalization within these simplified model liquid organelles can lead to enhanced metabolic rates under some conditions, but that very strong partitioning into the phase that serves as the compartment is necessary. In vivo, this could be provided by specific binding affinities between components of the liquid compartment and the molecules to be localized within it.
引用
收藏
页码:2182 / 2194
页数:13
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