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Impaired α-TTP-PIPs interaction underlies familial vitamin E deficiency.

Science. 2013 May 31;340(6136):1106-10. Epub 2013 Apr 18
Nozomu Kono 1 , Umeharu Ohto , Tatsufumi Hiramatsu , Michiko Urabe , Yasunori Uchida , Yoshinori Satow , Hiroyuki Arai
Nozomu Kono 1 , Umeharu Ohto , Tatsufumi Hiramatsu , Michiko Urabe , Yasunori Uchida , Yoshinori Satow , Hiroyuki Arai
+ et al

[No authors listed]

Author information
  • 1 Graduate School of Pharmaceutical Sciences, University of Tokyo, Tokyo, Japan.

摘要


α-Tocopherol (vitamin E) transfer protein (α-TTP) regulates the secretion of α-tocopherol from liver cells. Missense mutations of some arginine residues at the surface of α-TTP cause severe vitamin E deficiency in humans, but the role of these residues is unclear. Here, we found that wild-type α-TTP bound phosphatidylinositol phosphates (PIPs), whereas the arginine mutants did not. In addition, PIPs in the target membrane promoted the intermembrane transfer of α-tocopherol by α-TTP. The crystal structure of the α-TTP-PIPs complex revealed that the disease-related arginine residues interacted with phosphate groups of the PIPs and that the PIPs binding caused the lid of the α-tocopherol-binding pocket to open. Thus, PIPs have a role in promoting the release of a ligand from a lipid-transfer protein.