Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations

Li, J. V.; Ng, C. A.; Cheng, D.; Yao, M.; Guo, Y.; Yu, Z.-Y.; Ramaswamy, Y.; Ju, L. A.; Kuchel, P. W.; Feneley, M. P.; Fatkin, D.; Cox, C. D.

doi:10.1101/2020.11.30.404962

bioRxiv · 10.1101/2020.11.30.404962

Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations

Li, J. V.·Ng, C. A.·Cheng, D.·Yao, M.·Guo, Y.·Yu, Z.-Y.·Ramaswamy, Y.·Ju, L. A.·Kuchel, P. W.·Feneley, M. P.·Fatkin, D.·Cox, C. D.

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Abstract

Mechanosensitive channels are integral membrane proteins that sense mechanical stimuli. Like all membrane proteins, they pass through biosynthetic quality control in the endoplasmic reticulum and Golgi that results in them reaching their destination at the plasma membrane. Here we show that N-linked glycosylation of two highly conserved asparagine residues in the cap region of mechanosensitive Piezo1 channels are necessary for the mature protein to reach the plasma membrane. Both mutation of these asparagines (N2294Q/N2331Q) and treatment with an enzyme that hydrolyses N-linked oligosaccharides (PNGaseF) eliminates the fully glycosylated mature Piezo1 protein. The N-glycans in the cap are a pre-requisite for higher-order glycosylation in the propeller regions, which are present in loops that are essential for mechanotransduction. Importantly, trafficking-defective Piezo1 variants linked to generalized lymphatic dysplasia and bicuspid aortic valve display reduced fully N-glycosylated protein. The higher order glycosylation status in vitro correlates with efficient membrane trafficking and will aid in determining the functional impact of Piezo1 variants of unknown significance.

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Li, J. V., Ng, C. A., Cheng, D., Yao, M., Guo, Y., Yu, Z.-Y., Ramaswamy, Y., Ju, L. A., Kuchel, P. W., Feneley, M. P., Fatkin, D., Cox, C. D.. 2020-12-01. Modified N-linked glycosylation status predicts trafficking defective human Piezo1 channel mutations. https://doi.org/10.1101/2020.11.30.404962

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