Article ID Journal Published Year Pages File Type
1981627 FEBS Open Bio 2015 7 Pages PDF
Abstract

•The aquaporin 2 mutation V71M causes nephrogenic diabetes insipidus in humans.•Val71 is highly conserved in aqua(glycero)porins and points into the translocation pore.•The V71M mutation does not impair the activity and oligomerization of a bacterial homolog.

Several point mutations have been identified in human aquaporins, but their effects on the function of the respective aquaporins are mostly enigmatic. We analyzed the impact of the aquaporin 2 mutation V71M, which causes nephrogenic diabetes insipidus in humans, on aquaporin structure and activity, using the bacterial aquaglyceroporin GlpF as a model. Importantly, the sequence and structure around the V71M mutation is highly conserved between aquaporin 2 and GlpF. The V71M mutation neither impairs substrate flux nor oligomerization of the aquaglyceroporin. Therefore, the human aquaporin 2 mutant V71M is most likely active, but cellular trafficking is probably impaired.

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Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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