Current Research Interests
Our goal is to understand the linkage between dysfunctional SEC14-like proteins and human diseases. In particular, we try to understand how members of the SEC14-like family of proteins recognize and shuttle specific lipids between compartments. Besides the biophysical aspects of targeted lipid-transfer we aim to understand how human retinopathies and neurological disorders are associated with missense mutations of the carriers.
Major research projects
- Vitamin E retention and homeostasis
- The role of Vitamin A binding proteins in the chemistry of vision
- Modulation of cholesterol endosynthesis by SEC14-like proteins