Deciphering How Clustered O‑Glycosylation Shapes Substrate-Binding Preferences in an Intrinsically Disordered Protein Region

解析簇状 O-糖基化如何影响固有无序蛋白区域的底物结合偏好

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Abstract

Post-translational modifications such as clustered O-glycosylation are frequently enriched in intrinsically disordered regions (IDRs), yet their roles in shaping molecular behavior and functional specificity remain poorly understood. Here, we addressed this challenge through an integrative, stepwise strategy that combines chemical synthesis, experimental characterization, and molecular dynamics (MD) simulations, employing the extensively O-mannosylated linker of Trichoderma reesei Family 7 cellobiohydrolase as a model IDR. Using synthetically accessible linker glycoforms bearing monomannose residues, we showed that unglycosylated and partially glycosylated linkers strongly prefer lignin over cellulose, driven by electrostatic interactions with the negatively charged lignin surface. Increasing glycan density or glycan size, such as through the introduction of dimannose, weakens lignin binding and partially shifts binding preference toward cellulose. Importantly, MD simulations informed and validated by these experimental data enabled prediction of currently synthetically inaccessible glycoforms, revealing that negatively charged glycans, such as phosphorylated mannose, effectively abolish lignin affinity while largely preserving cellulose binding. This work provides a generalizable and predictive framework for elucidating how complex glycosylation patterns regulate IDR-ligand interactions and identifies charge-mediated modulation as a key mechanism through which clustered O-glycosylation tunes IDR function.

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