Clathrin-mediated endocytosis (CME) proceeds through a series of morphological changes of the plasma membrane induced by a number of protein components. Although the spatiotemporal assembly of these proteins has been elucidated by fluorescence-based techniques, the protein-induced morphological changes of the plasma membrane have not been fully clarified in living cells. Here we visualize membrane morphology together with protein localizations during CME by utilizing high-speed atomic force microscopy combined with a confocal laser scanning unit. The plasma membrane starts to invaginate ~30 seconds after clathrin starts to assemble, and the aperture diameter increases as clathrin accumulates. Actin rapidly accumulates around the pit and induces a small membrane swelling, which within 30 seconds rapidly covers the pit irreversibly. Inhibition of actin turnover abolishes the swelling and induces a reversible open-close motion of the pit, indicating that actin dynamics are necessary for efficient and irreversible pit closure at the end of the CME.
Morphological changes of plasma membrane and protein assembly during clathrin-mediated endocytosis
A. Yoshida,Nobuaki Sakai,Yoshitsugu Uekusa,Yuka Imaoka,Yoshitsuna Itagaki,Yuki Suzuki,S. Yoshimura
Published 2017 in bioRxiv
ABSTRACT
PUBLICATION RECORD
- Publication year
2017
- Venue
bioRxiv
- Publication date
2017-10-31
- Fields of study
Biology, Medicine, Chemistry
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
CITATION MAP
EXTRACTION MAP
CLAIMS
- No claims are published for this paper.
CONCEPTS
- No concepts are published for this paper.
REFERENCES
Showing 1-83 of 83 references · Page 1 of 1
CITED BY
Showing 1-63 of 63 citing papers · Page 1 of 1