Large self-assembled clathrin lattices spontaneously disassemble without sufficient adaptor proteins

• Published in: PLoS computational biology Vol. 18; no. 3; p. e1009969
• Main Authors: Guo, Si-Kao, Sodt, Alexander J, Johnson, Margaret E
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.03.2022; Public Library of Science (PLoS)
• Subjects: Abundance; Adapters; Adaptor proteins; Adaptor Proteins, Signal Transducing - metabolism; Bending; Binding sites; Biology and Life Sciences; Cell Membrane - metabolism; Cell membranes; Clathrin; Clathrin - chemistry; Dismantling; Endocytosis; Energy consumption; Experiments; Health aspects; Kinetics; Lattices; Localization; Measurement; Membranes; Nucleation; Physical Sciences; Proteins; Self assembly; Simulation; Software; Stoichiometry; United States
• ISSN: 1553-7358; 1553-734X; 1553-7358
• DOI: 10.1371/journal.pcbi.1009969

Clathrin-coated structures must assemble on cell membranes to internalize receptors, with the clathrin protein only linked to the membrane via adaptor proteins. These structures can grow surprisingly large, containing over 20 clathrin, yet they often fail to form productive vesicles, instead aborting and disassembling. We show that clathrin structures of this size can both form and disassemble spontaneously when adaptor protein availability is low, despite high abundance of clathrin. Here, we combine recent in vitro kinetic measurements with microscopic reaction-diffusion simulations and theory to differentiate mechanisms of stable vs unstable clathrin assembly on membranes. While in vitro conditions drive assembly of robust, stable lattices, we show that concentrations, geometry, and dimensional reduction in physiologic-like conditions do not support nucleation if only the key adaptor AP-2 is included, due to its insufficient abundance. Nucleation requires a stoichiometry of adaptor to clathrin that exceeds 1:1, meaning additional adaptor types are necessary to form lattices successfully and efficiently. We show that the critical nucleus contains ~25 clathrin, remarkably similar to sizes of the transient and abortive structures observed in vivo. Lastly, we quantify the cost of bending the membrane under our curved clathrin lattices using a continuum membrane model. We find that the cost of bending the membrane could be largely offset by the energetic benefit of forming curved rather than flat structures, with numbers comparable to experiments. Our model predicts how adaptor density can tune clathrin-coated structures from the transient to the stable, showing that active energy consumption is therefore not required for lattice disassembly or remodeling during growth, which is a critical advance towards predicting productive vesicle formation.