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PMID: 20729836 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Coupling between clathrin-dependent endocytic budding and F-BAR-dependent tubulation in a cell-free system.

Nature cell biology ·Vol. 12 ·No. 9 ·2010-09-00 ·Pages 902-8

Wu M, Huang B, Graham M, Raimondi A, Heuser JE, Zhuang X, De Camilli P

Abstract

Cell-free reconstitution of membrane traffic reactions and the morphological characterization of membrane intermediates that accumulate under these conditions have helped to elucidate the physical and molecular mechanisms involved in membrane transport. To gain a better understanding of endocytosis, we have reconstituted vesicle budding and fission from isolated plasma membrane sheets and imaged these events. Electron and fluorescence microscopy, including subdiffraction-limit imaging by stochastic optical reconstruction microscopy (STORM), revealed F-BAR (FBP17) domain coated tubules nucleated by clathrin-coated buds when fission was blocked by GTPgammaS. Triggering fission by replacing GTPgammaS with GTP led not only to separation of clathrin-coated buds, but also to vesicle formation by fragmentation of the tubules. These results suggest a functional link between FBP17-dependent membrane tubulation and clathrin-dependent budding. They also show that clathrin spatially directs plasma membrane invaginations that lead to the generation of endocytic vesicles larger than those enclosed by the coat.

MeSH Terms
Actins/antagonists & inhibitors Acyltransferases/metabolism Adenosine Triphosphate/pharmacology Animals Antibodies/immunology,pharmacology Bridged Bicyclo Compounds, Heterocyclic/pharmacology Carrier Proteins/immunology,metabolism Cattle Cell Line Cell Membrane/drug effects,physiology,ultrastructure Cell Membrane Structures/drug effects,physiology,ultrastructure Cell-Free System/drug effects,physiology Clathrin/immunology,metabolism Coated Pits, Cell-Membrane/drug effects,physiology,ultrastructure Cytosol/metabolism Dynamins/metabolism Endocytosis/drug effects,physiology Fatty Acid-Binding Proteins Fibroblasts Guanosine 5'-O-(3-Thiotriphosphate)/pharmacology Guanosine Triphosphate/pharmacology Humans Imaging, Three-Dimensional/methods Mice Microscopy, Electron, Transmission Microscopy, Fluorescence Models, Biological Potoroidae Rats Receptors, Transferrin/metabolism Thiazolidines/pharmacology
Chemicals
Actins Antibodies Bridged Bicyclo Compounds, Heterocyclic Carrier Proteins Clathrin FNBP1 protein, human Fatty Acid-Binding Proteins Receptors, Transferrin Thiazolidines Guanosine 5'-O-(3-Thiotriphosphate) Guanosine Triphosphate Adenosine Triphosphate Acyltransferases 2-acylglycerophosphate acyltransferase Dynamins latrunculin B
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Wu Min
Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06520, USA.
Huang Bo
Graham Morven
Raimondi Andrea
Heuser John E
Zhuang Xiaowei
De Camilli Pietro
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Article Info
Journal
Nature cell biology
Abbr.
Nat Cell Biol
ISSN
1476-4679
Published
2010-09-00
Epub
2010-00-22
Pages
902-8
Language
English
Region
England
NLM ID
100890575
PMCID
PMC3338250
Subset
IM
Grants
NIGMS NIH HHS · R01 GM068518 · United States
Howard Hughes Medical Institute · United States
NIDA NIH HHS · P30 DA018343 · United States
NIDDK NIH HHS · DK45735 · United States
NIDDK NIH HHS · P30 DK045735 · United States
NINDS NIH HHS · R01 NS036251 · United States
NIGMS NIH HHS · GM068518 · United States
NINDS NIH HHS · NS36251 · United States
NINDS NIH HHS · R37 NS036251 · United States
NINDS NIH HHS · R37 NS036251-15 · United States
Corrections
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