Intrinsic disorder accelerates dissociation rather than association

Koji Umezawa, Jun Ohnuki, Junichi Higo, Mitsunori Takano

    Research output: Contribution to journalArticlepeer-review

    19 Citations (Scopus)


    The intrinsically disordered protein (IDP) has distinct properties both physically and biologically: it often becomes folded when binding to the target and is frequently involved in signal transduction. The physical property seems to be compatible with the biological property where fast association and dissociation between IDP and the target are required. While fast association has been well studied, fueled by the fly-casting mechanism, the dissociation kinetics has received less attention. We here study how the intrinsic disorder affects the dissociation kinetics, as well as the association kinetics, paying attention to the interaction strength at the binding site (i.e., the quality of the “fly lure”). Coarse-grained molecular dynamics simulation of the pKID-KIX system, a well-studied IDP system, shows that the association rate becomes larger as the disorder-inducing flexibility that was imparted to the model is increased, but the acceleration is marginal and turns into deceleration as the quality of the fly lure is worsened. In contrast, the dissociation rate is greatly enhanced as the disorder is increased, indicating that intrinsic disorder serves for rapid signal switching more effectively through dissociation than association. Proteins 2016; 84:1124–1133.

    Original languageEnglish
    Pages (from-to)1124-1133
    Number of pages10
    JournalProteins: Structure, Function and Genetics
    Issue number8
    Publication statusPublished - 2016 Aug 1


    • capture radius
    • coarse-grained model
    • coupled folding and binding
    • flexibility
    • fly-casting mechanism
    • Langevin dynamics
    • molecular dynamics simulation
    • phosphorylation
    • signaling

    ASJC Scopus subject areas

    • Biochemistry
    • Structural Biology
    • Molecular Biology

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