Structural basis of the lipid transfer mechanism of phospholipid transfer protein (PLTP) |
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Authors: | Meng Zhang Xiaobo Zhai Jinping Li John J. Albers Simona Vuletic Gang Ren |
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Affiliation: | 1. The Molecular Foundry, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, United States;2. Department of Biomedical Science, Mercer University School of Medicine, Savannah, GA 31404, United States;3. Northwest Lipid Metabolism and Diabetes Research Laboratories, Seattle, WA 98109, United States |
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Abstract: | Human phospholipid transfer protein (PLTP) mediates the transfer of phospholipids among atheroprotective high-density lipoproteins (HDL) and atherogenic low-density lipoproteins (LDL) by an unknown mechanism. Delineating this mechanism would represent the first step towards understanding PLTP-mediated lipid transfers, which may be important for treating lipoprotein abnormalities and cardiovascular disease. Here, using various electron microscopy techniques, PLTP is revealed to have a banana-shaped structure similar to cholesteryl ester transfer protein (CETP). We provide evidence that PLTP penetrates into the HDL and LDL surfaces, respectively, and then forms a ternary complex with HDL and LDL. Insights into the interaction of PLTP with lipoproteins at the molecular level provide a basis to understand the PLTP-dependent lipid transfer mechanisms for dyslipidemia treatment. |
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Keywords: | PLTP Phospholipid transfer protein PLTP bound to HDL PLTP bound to liposome Electron microscopy HDL Liposome |
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