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arXiv · 0805.0835

Mechanism of robust circadian oscillation of KaiC phosphorylation in vitro

Kohei Eguchi·Mitsumasa Yoda·Tomoki P. Terada·Masaki Sasai
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Abstract

By incubating the mixture of three cyanobacterial proteins, KaiA, KaiB, and KaiC, with ATP in vitro, Kondo and his colleagues reconstituted the robust circadian rhythm of the phosphorylation level of KaiC (Science, 308; 414-415 (2005)). This finding indicates that protein-protein interactions and the associated hydrolysis of ATP suffice to generate the circadian rhythm. Several theoretical models have been proposed to explain the rhythm generated in this "protein-only" system, but the clear criterion to discern different possible mechanisms was not known. In this paper, we discuss a model based on the two basic assumptions: The assumption of the allosteric transition of a KaiC hexamer and the assumption of the monomer exchange between KaiC hexamers. The model shows a stable rhythmic oscillation of the phosphorylation level of KaiC, which is robust against changes in concentration of Kai proteins. We show that this robustness gives a clue to distinguish different possible mechanisms. We also discuss the robustness of oscillation against the change in the system size. Behaviors of the system with the cellular or subcellular size should shed light on the role of the protein-protein interactions in in vivo circadian oscillation.

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Kohei Eguchi, Mitsumasa Yoda, Tomoki P. Terada, Masaki Sasai. 2008-05-07. Mechanism of robust circadian oscillation of KaiC phosphorylation in vitro. https://doi.org/10.1529/biophysj.107.127555

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