Identification and functional analyses of disease-associated P4-ATPase phospholipid flippase variants in red blood cells

Angela Y Liou, Laurie L Molday, Jiao Wang, Jens Peter Andersen, Robert S Molday

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisTidsskriftartikelForskningpeer review

Abstract

ATP-dependent phospholipid flippase activity crucial for generating lipid asymmetry was first detected in red blood cell (RBC) membranes, but the P4-ATPases responsible have not been directly determined. Using affinity-based MS, we show that ATP11C is the only abundant P4-ATPase phospholipid flippase in human RBCs, whereas ATP11C and ATP8A1 are the major P4-ATPasesinmouse RBCs. Wealso found that ATP11A and ATP11B are present at low levels. Mutations in the gene encoding ATP11C are responsible for blood and liver disorders, but the disease mechanisms are not known. Using heterologous expression, we show that the T415N substitution in the phosphorylation motif of ATP11C, responsible for congenital hemolytic anemia, reduces ATP11C expression, increases retention in the endoplasmic reticulum, and decreases ATPase activity by 61% relative to WT ATP11C. The I355K substitution in the transmembrane domain associated with cholestasis and anemia in mice was expressed at WT levels and trafficked to the plasma membrane but was devoid of activity. We conclude that the T415N variant causes significant protein misfolding, resulting in low protein expression, cellular mislocalization, and reduced functional activity. In contrast, the I355K variant folds and traffics normally but lacks key contacts required for activity. We propose that the loss in ATP11C phospholipid flippase activity coupled with phospholipid scramblase activity results in the exposure of phosphatidylserine on the surface of RBCs, decreasing RBC survival and resulting in anemia.

OriginalsprogEngelsk
TidsskriftJournal of Biological Chemistry
Vol/bind294
Nummer17
Sider (fra-til)6809-6821
Antal sider13
ISSN0021-9258
DOI
StatusUdgivet - apr. 2019

Fingeraftryk

Dyk ned i forskningsemnerne om 'Identification and functional analyses of disease-associated P4-ATPase phospholipid flippase variants in red blood cells'. Sammen danner de et unikt fingeraftryk.

Citationsformater