Site-specific O-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactions

Wang, S. ; Mao, Y. ; Narimatsu, Y. ; Ye, Z. ; Tian, W. ; Goth, C.K. ; Lira-Navarrete, E. ; Pedersen, N.B. ; Benito-Vicente, A. ; Martin, C. ; Uribe, K.B. ; Hurtado-Guerrero, R. (Universidad de Zaragoza) ; Christoffersen, C. ; Seidah, N.G. ; Nielsen, R. ; Christensen, E.I. ; Hansen, L. ; Bennett, E.P. ; Vakhrushev, S.Y. ; Schjoldager, K.T. ; Clausen, H.

Resumen: The low-density lipoprotein receptor (LDLR) and related receptors are important for the transport of diverse biomolecules across cell membranes and barriers. Their functions are especially relevant for cholesterol homeostasis and diseases, including neurodegenerative and kidney disorders. Members of the LDLR-related protein family share LDLR class A (LA) repeats providing binding properties for lipoproteins and other biomolecules. We previously demonstrated that short linker regions between these LA repeats contain conserved O-glycan sites. Moreover, we found that O-glycan modifications at these sites are selectively controlled by the GalNAc-transferase isoform, GalNAc-T11. However, the effects of GalNAc-T11–mediated O-glycosylation on LDLR and related receptor localization and function are unknown. Here, we characterized O-glycosylation of LDLR-related proteins and identified conserved O-glycosylation sites in the LA linker regions of VLDLR, LRP1, and LRP2 (Megalin) from both cell lines and rat organs. Using a panel of gene-edited isogenic cell line models, we demonstrate that GalNAc-T11–mediated LDLR and VLDLR O-glycosylation is not required for transport and cell-surface expression and stability of these receptors but markedly enhances LDL and VLDL binding and uptake. Direct ELISA-based binding assays with truncated LDLR constructs revealed that O-glycosylation increased affinity for LDL by 5-fold. The molecular basis for this observation is currently unknown, but these findings open up new avenues for exploring the roles of LDLR-related proteins in disease.

Idioma: Inglés

DOI: 10.1074/jbc.M117.817981

Año: 2018

Publicado en: Journal of Biological Chemistry 293, 19 (2018), 7408-7422
ISSN: 0021-9258

Factor impacto SCIMAGO: 2.403 - Biochemistry (Q1) - Molecular Biology (Q1) - Cell Biology (Q1)

Tipo y forma: Article (Published version)

Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)