4.8 Article

The TPLATE complex mediates membrane bending during plant clathrin-mediated endocytosis

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2113046118

Keywords

clathrin-mediated endocytosis; TPLATE; Arabidopsis; membrane remodeling

Funding

  1. Austrian Science Fund [I3630B25]
  2. Agence Nationale de la Recherche [ANR-11-EQPX-0029, ANR-10-INBS-04]
  3. NSF [1121998, 1614915]
  4. European Research Council [682436]
  5. China Scholarship Council [201508440249]
  6. Ghent University Special Research [ST01511051]
  7. Scientific Service Units of Institute of Science and Technology Austria (IST Austria)
  8. Direct For Biological Sciences
  9. Div Of Molecular and Cellular Bioscience [1614915] Funding Source: National Science Foundation

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This study identified the TPLATE complex as a key component in the unique plant endocytosis mechanism, playing a crucial role in mediating membrane bending against high-turgor pressure in plant cells.
Clathrin-mediated endocytosis is the major route of entry of cargos into cells and thus underpins many physiological processes. During endocytosis, an area of flat membrane is remodeled by proteins to create a spherical vesicle against intracellular forces. The protein machinery which mediates this membrane bending in plants is unknown. However, it is known that plant endocytosis is actin independent, thus indicating that plants utilize a unique mechanism to mediate membrane bending against high-turgor pressure compared to other model systems. Here, we investigate the TPLATE complex, a plant-specific endocytosis protein complex. It has been thought to function as a classical adaptor functioning underneath the clathrin coat. However, by using biochemical and advanced live microscopy approaches, we found that TPLATE is peripherally associated with clathrin-coated vesicles and localizes at the rim of endocytosis events. As this localization is more fitting to the protein machinery involved in membrane bending during endocytosis, we examined cells in which the TPLATE complex was disrupted and found that the clathrin structures present as flat patches. This suggests a requirement of the TPLATE complex for membrane bending during plant clathrin-mediated endocytosis. Next, we used in vitro biophysical assays to confirm that the TPLATE complex possesses protein domains with intrinsic membrane remodeling activity. These results redefine the role of the TPLATE complex and implicate it as a key component of the evolutionarily distinct plant endocytosis mechanism, which mediates endocytic membrane bending against the high-turgor pressure in plant cells.

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