A Design Principle for a Posttranslational Biochemical Oscillator

SummaryMultisite phosphorylation plays an important role in biological oscillators such as the circadian clock. Its general role, however, has been elusive. In this theoretical study, we show that a simple substrate with two modification sites acted upon by two opposing enzymes (e.g., a kinase and a phosphatase) can show oscillations in its modification state. An unbiased computational analysis of this oscillator reveals two common characteristics: a unidirectional modification cycle and sequestering of an enzyme by a specific modification state. These two motifs cause a substrate to act as a coupled system in which a unidirectional cycle generates single-molecule oscillators, whereas sequestration synchronizes the population by limiting the available enzyme under conditions in which substrate is in excess. We also demonstrate the conditions under which the oscillation period is temperature compensated, an important feature of the circadian clock. This theoretical model will provide a framework for analyzing and synthesizing posttranslational oscillators.

Graphical AbstractFigure optionsDownload as PowerPoint slideHighlights
► Multisite substrate modifications can oscillate with two opposing enzymes
► Oscillation requires a unidirectional modification cycle and enzyme sequestration
► Coupling of single-molecule oscillators is a design principle
► The period of oscillation can be temperature compensated