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The interdomain flexible linker of the polypeptide GalNAc transferases dictates their long-range glycosylation preferences.

Matilde de Las Rivas | Erandi Lira-Navarrete | Earnest James Paul Daniel | Ismael Compañón | Helena Coelho | Ana Diniz | Jesús Jiménez-Barbero | Jesús M Peregrina | Henrik Clausen | Francisco Corzana | Filipa Marcelo | Gonzalo Jiménez-Osés | Thomas A Gerken | Ramon Hurtado-Guerrero
Nature communications | 2017

The polypeptide GalNAc-transferases (GalNAc-Ts), that initiate mucin-type O-glycosylation, consist of a catalytic and a lectin domain connected by a flexible linker. In addition to recognizing polypeptide sequence, the GalNAc-Ts exhibit unique long-range N- and/or C-terminal prior glycosylation (GalNAc-O-Ser/Thr) preferences modulated by the lectin domain. Here we report studies on GalNAc-T4 that reveal the origins of its unique N-terminal long-range glycopeptide specificity, which is the opposite of GalNAc-T2. The GalNAc-T4 structure bound to a monoglycopeptide shows that the GalNAc-binding site of its lectin domain is rotated relative to the homologous GalNAc-T2 structure, explaining their different long-range preferences. Kinetics and molecular dynamics simulations on several GalNAc-T2 flexible linker constructs show altered remote prior glycosylation preferences, confirming that the flexible linker dictates the rotation of the lectin domain, thus modulating the GalNAc-Ts' long-range preferences. This work for the first time provides the structural basis for the different remote prior glycosylation preferences of the GalNAc-Ts.

Pubmed ID: 29208955

Research resources used in this publication

None found

Antibodies used in this publication

None found

Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM113534
  • Agency: NIGMS NIH HHS, United States
    Id: U01 GM113534

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