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bioRxiv · 10.1101/2021.05.28.446235

Integration and comparison of multi-omics profiles of NGLY1 deficiency plasma and cellular models to identify clinically relevant molecular phenotypes

Chen, S.·Wang, G.·Shen, X.·Hornburg, D.·Hoffman, R.·Nevins, S.·Cheng, X.·Snyder, M.
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Abstract

NGLY1 (N-glycanase 1) deficiency is a rare congenital recessive disorder of protein deglycosylation unaddressed by the current standard of care. Using combined metabolomics and proteomics profiling, we show that NGLY1 deficiency activates the immune response and disturbs lipid metabolism, biogenic amine synthesis, and glutathione metabolism. These alterations were also observed in NGLY1 deficient patient-derived induced pluripotent stem cells (iPSCs) and differentiated neural progenitor cells (NPCs), which serve as personalized cellular models of the disease. These findings provide molecular insight into the pathophysiology of NGLY1 deficiency and suggest potential therapeutic strategies.

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Chen, S., Wang, G., Shen, X., Hornburg, D., Hoffman, R., Nevins, S., Cheng, X., Snyder, M.. 2021-05-28. Integration and comparison of multi-omics profiles of NGLY1 deficiency plasma and cellular models to identify clinically relevant molecular phenotypes. https://doi.org/10.1101/2021.05.28.446235

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