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. 2019 May 24;294(21):8349. doi: 10.1074/jbc.AAC119.009121

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

Shengjun Wang, Yang Mao, Yoshiki Narimatsu, Zilu Ye, Weihua Tian, Christoffer K Goth, Erandi Lira-Navarrete, Nis B Pedersen, Asier Benito-Vicente, Cesar Martin, Kepa B Uribe, Ramon Hurtado-Guerrero, Christina Christoffersen, Nabil G Seidah, Rikke Nielsen, Erik I Christensen, Lars Hansen, Eric P Bennett, Sergey Y Vakhrushev, Katrine T Schjoldager, Henrik Clausen
PMCID: PMC6544857  PMID: 31127061

VOLUME 293 (2018) PAGES 7408–7422

In Fig. 6B, the separation lines between the gel lanes were poorly reproduced. Samples were run in the same gel and only select lanes are shown. In Fig. S3, the merged control picture (upper right panel) was inadvertently taken from a repeat experiment. The “Experimental procedures” inadvertently left out details of the controls used for FACS experiments. In Fig. 2C, the labeled negative control refers to binding of the secondary antibody swine anti-rabbit IgG without preincubation with the rabbit anti-LDLR antibody. In Fig. 3, the labeled control refers to HepG2 WT cells incubated without Dil-LDL, and the same control was used in Figs. S2 and S3. In Fig. 4B, the labeled negative control refers to HEK293 WT cells incubated without FITC-LDL. In Fig. 4, C and D, the labeled control refers to CHO WT cells incubated without Dil-LDL. These errors have now been corrected and do not affect the results or conclusions of this work.

Figure 6B.

Figure 6B.

Figure S3.

Figure S3.


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