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Inhibition of N-glycanase1 induces autophagic clearance of protein aggregates

Needs, Sarah; Bootman, Martin; Alonzi, Dominic and Allman, Sarah (2016). Inhibition of N-glycanase1 induces autophagic clearance of protein aggregates. In: Glycobiology, 26(12) pp. 1351–1499.

DOI (Digital Object Identifier) Link: https://doi.org/10.1093/glycob/cww110
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Abstract

Quality control of protein folding is crucial to the maintenance of cellular homeostasis. Impairment of these systems and the related degradative pathways involved in the clearance of misfolded proteins can result in severe and varied pathologies. Peptide N-glycanase (EC 3.5.1.52) is an endoglycosidase which cleaves N-linked glycans from incorrectly folded glycoproteins exported from the endoplasmic reticulum and occurs prior to degradation by the 26S proteasome and is important for the degradation of misfolded glycoproteins during ER-associated degradation. Mutations in this enzyme are responsible for the rare disorder, N-GLY1, a congenital multi-system disorder which results in a build-up of protein aggregates in the cell cytosol. Using a pharmacological inhibitor of peptide N-glycanase, carbobenzoxy-valyl-ananyl-aspartyl-[O-methyl]-fluoromethylketone (Z-VAD-fmk), we have found that inhibition of Nglycanase using 50 µM Z-VAD-fmk resulted in an increase in Thioflavin T fluorescence intensity after 48 hours which decreases to near basal levels after 72 hours. Thioflavin T is a fluorescent dye that exhibits enhanced fluorescence upon binding to β-sheets, characteristic of aggregated structures and fibril formation. Changes in characteristic ER stress markers were also observed; variation in the expression of BiP (GRP78), which is increased during the unfolded protein response, was observed to correlate with the changes in Thioflavin T fluorescence. Using a GFP-LC3 reporter in HEK cells we found an increase in autophagy after 72 hours of peptide N-glycanase inhibition. The increase in autophagy corresponded to the decrease in Thioflavin T fluorescence and variation in BiP levels, suggesting that protein aggregates were removed by the induction of autophagy when deglycosylation is impaired. In an autophagy deficient cell line, ATG13-/- MEFs, we found inhibition of peptide N-glycanase by 50 µM Z-VAD-fmk lead to a 45 % decrease in cell viability within 24 hours with no loss of viability seen in the corresponding wild type MEFs or HEK cells. These results show that autophagy is essential for removal of protein aggregates resulting from the inhibition of peptide N-glycanase. Further work will focus on the investigation of the autophagic machinery linked to clearance of protein aggregates caused by peptide N-glycanase inhibition.

Item Type: Conference or Workshop Item
ISSN: 0959-6658
Academic Unit/School: Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
Other Departments > Research and Academic Strategy
Other Departments
Interdisciplinary Research Centre: Biomedical Research Network (BRN)
Health and Wellbeing PRA (Priority Research Area)
Related URLs:
Item ID: 47837
Depositing User: Sarah Allman
Date Deposited: 16 Nov 2016 16:07
Last Modified: 11 Sep 2017 15:32
URI: http://oro.open.ac.uk/id/eprint/47837
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