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• W2057688655 abstract "Neuronal Kv3 voltage-gated K+ channels have two absolutely conserved N-glycosylation sites. Here, it is shown that Kv3.1, 3.3, and 3.4 channels are N-glycosylated in rat brain. Digestion of total brain membranes with peptide N glycosidase F (PNGase F) produced faster migrating immunobands than those of undigested membranes. Additionally, partial PNGase F digests showed that both sites are occupied by oligosaccharides. Neuraminidase treatment produced a smaller immunoband shift relative to PNGase F treatment. These results indicate that both sites are highly available and occupied by N-linked oligosaccharides for Kv3.1, 3.3, and 3.4 in rat brain, and furthermore that at least one oligosaccharide is of complex type. Additionally, these results point to an extracytoplasmic S1–S2 linker in Kv3 proteins expressed in native membranes. We suggest that N-glycosylation processing of Kv3 channels is critical for the expression of K+ currents at the surface of neurons, and perhaps contributes to the pathophysiology of congenital disorders of glycosylation." @default.
• W2057688655 created "2016-06-24" @default.
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• W2057688655 date "2007-04-01" @default.
• W2057688655 modified "2023-10-15" @default.
• W2057688655 title "Complex oligosaccharides are N-linked to Kv3 voltage-gated K+ channels in rat brain" @default.
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• W2057688655 doi "https://doi.org/10.1016/j.bbagen.2006.11.013" @default.
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