Molecular tag for promoting N-glycan maturation in the cargo receptor-mediated secretion pathway

MCFD2 and ERGIC-53 form a cargo receptor complex that plays a crucial role in transporting specific glycoproteins, including blood coagulation factor VIII, from the endoplasmic reticulum to the Golgi apparatus. We have demonstrated that MCFD2 recognizes a 10-amino-acid sequence in factor VIII, thereby facilitating its efficient transport. Moreover, the secretion of biopharmaceutical recombinant glycoproteins, such as erythropoietin, can be enhanced by tagging them with this sequence, which we have termed the “passport sequence” (PS). Here, we found that the PS promotes the galactosylation and sialylation of N-glycans on glycoproteins. Furthermore, we discovered that glycoproteins tagged with the PS follow a unique route in the Golgi, where they encounter NUCB1. NUCB1 also recognizes the PS and mediates its interaction with the galactosylation enzyme B4GALT1. These findings offer a promising strategy for controlling the glycosylation of recombinant glycoproteins of biopharmaceutical interest. [Display omitted] •The passport sequence promotes N-glycan maturation of recombinant glycoproteins•The passport sequence directs glycoproteins to interact with NUCB1 in Golgi•NUCB1 mediates the interaction of glycoproteins with galactosylation enzyme•This offers a novel strategy to control glycosylation of biopharmaceutical proteins Biochemistry; Protein; Properties of biomolecules; Glycobiology; Molecular biology