Quantifications of FCHo2 interaction with in vitro and in cellulo systems
Data files
Feb 15, 2022 version files 2.33 MB
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ElAlaoui_2022_a_Intensity_PIP2_membranes.xlsx
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ElAlaoui_2022_b_Intensity_PIP2_cells.xlsx
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ElAlaoui_2022_c_Norm_Intensity_PIP2_Cytosol.xlsx
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ElAlaoui_2022_d_Norm_Intensity_Clathrin_Cytosol.xlsx
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ElAlaoui_2022_e_Size_clusters_fluo.xlsx
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ElAlaoui_2022_f_Size_clusters_AFM.xlsx
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ElAlaoui_2022_g_Height_clusters_AFM.xlsx
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ElAlaoui_2022_h_Distance_FCHo2_AFM.xlsx
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ElAlaoui_2022_i_Docking_FCHo2_AFM.xlsx
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ElAlaoui_2022_j_Binding_FCHo2_bilayers.xlsx
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ElAlaoui_2022_k_Binding_FBAR_bilayers.xlsx
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ElAlaoui_2022_l_Intensity_FCHo2_bilayers.xlsx
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ElAlaoui_2022_m_Intensity_FBAR_bilayers.xlsx
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ElAlaoui_2022_n_Lifetime_FCHo2_bilayers.xlsx
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ElAlaoui_2022_o_Intensity_Clathrin_bilayers.xlsx
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ELALAOUI_2022_README.txt
Abstract
Clathrin-mediated endocytosis (CME) is a central trafficking pathway in eukaryotic cells regulated by phosphoinositides. The plasma membrane phosphatidylinositol-4,5-bisphosphate (PI(4,5)P2) plays an instrumental role in driving CME initiation. The F-BAR domain only protein 1 and 2 complex (FCHo1/2) is among the early proteins that reach the plasma membrane, but the exact mechanisms triggering its recruitment remain elusive. Here, we show the molecular dynamics of FCHo2 self-assembly on membranes by combining minimal reconstituted in vitro and cellular systems. Our results indicate that PI(4,5)P2 domains assist FCHo2 docking at specific membrane regions, where it self-assembles into ring-like shape protein patches. We show that the binding of FCHo2 on cellular membranes promotes PI(4,5)P2 clustering at the boundary of cargo receptors and that this accumulation enhances clathrin assembly. Thus, our results provide a mechanistic framework that could explain the recruitment of early PI(4,5)P2-interacting proteins at endocytic sites.