Coassembly of flotillins induces formation of membrane microdomains, membrane curvature, and vesicle budding |
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Authors: | Frick Manfred Bright Nicholas A Riento Kirsi Bray Aurélie Merrified Christien Nichols Benjamin J |
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Institution: | Medical Research Council Laboratory of Molecular Biology, Cambridge, UK. |
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Abstract: | Endocytosis has a crucial role in many cellular processes. The best-characterized mechanism for endocytosis involves clathrin-coated pits 1], but evidence has accumulated for additional endocytic pathways in mammalian cells 2]. One such pathway involves caveolae, plasma-membrane invaginations defined by caveolin proteins. Plasma-membrane microdomains referred to as lipid rafts have also been associated with clathrin-independent endocytosis by biochemical and pharmacological criteria 3]. The mechanisms, however, of nonclathrin, noncaveolin endocytosis are not clear 4, 5]. Here we show that coassembly of two similar membrane proteins, flotillin1 and flotillin2 6-8], is sufficient to generate de novo membrane microdomains with some of the predicted properties of lipid rafts 9]. These microdomains are distinct from caveolin1-positive caveolae, are dynamic, and bud into the cell. Coassembly of flotillin1 and flotillin2 into microdomains induces membrane curvature, the formation of plasma-membrane invaginations morphologically similar to caveolae, and the accumulation of intracellular vesicles. We propose that flotillin proteins are defining structural components of the machinery that mediates a clathrin-independent endocytic pathway. Key attributes of this machinery are the dependence on coassembly of both flotillins and the inference that flotillin microdomains can exist in either flat or invaginated states. |
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