
Almost a century ago, plant extracts were documented to be critical for the fertility of rodents. This activity was later ascribed to vitamin E, a term comprising a number of structurally related plant lipids that function as fat soluble antioxidants. The alpha-tocopherol transfer protein (TTP) is a critical regulator of vitamin E status that stimulates the movement of vitamin E between membrane vesicles in vitro and facilitates the secretion of tocopherol from hepatocytes. Heritable mutations in the ttpA gene cause ataxia with vitamin E deficiency (AVED), an autosomal recessive disorder characterized by low plasma vitamin E levels and progressive neurodegeneration. This chapter summarizes recent advances in our understanding of the molecular and physiological aspects of TTP activity.
Models, Molecular, Sequence Homology, Amino Acid, Protein Conformation, Molecular Sequence Data, Rats, Mice, Animals, Humans, Vitamin E, Ataxia, Carrier Proteins
Models, Molecular, Sequence Homology, Amino Acid, Protein Conformation, Molecular Sequence Data, Rats, Mice, Animals, Humans, Vitamin E, Ataxia, Carrier Proteins
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