Table 1.
Reconstituted process or structure | Components used | References |
---|---|---|
Microspheres | ||
Cell motility | Listeria monocytogenes and NPF-coated microspheres immersed in Xenopus laevis extracts | 63,64 |
NPF-coated microspheres, actin, profilin, cofilin, Arp2/3 complex and capping protein | 22,23 | |
NPF-coated microspheres, actin, Arp2/3 complex and fascin | 25,24 | |
Mitotic spindle | DNA-coated microspheres and X. laevis cytoplasmic extracts | 20,65 |
Plasmid segregation | ParC coated microspheres, ParR and ParM | 27 |
Supported bilayers | ||
Immunological synapse | Supported bilayer containing MHC peptide and ICAM1, and T cells | 31,62 |
Neuronal synapse | Supported bilayer containing neuroligin 1, and neuronal cells | 32 |
Bacterial cell division | MinD and MinE | 33 |
Vesicle fission | Dynamin 1 and GTP | 35 |
Cell motility | Lipid-coated beads, N-WASP, actin, profilin, cofilin, Arp2/3 complex and capping protein | 34 |
Giant vesicles | ||
Bacterial cell division | Membrane-targeted FtsZ | 50 |
Membrane tube networks | Kinesin-bound GUV and microtubule tracks | 40,66 |
Actin–membrane interaction | PtdIns(4,5)P2-containing vesicles, actin, N-WASP and Arp2/3 complex | 46 |
Filopodia formation | PtdIns(4,5)P2-containing vesicles, actin, N-WASP and Arp2/3 complex | 48 |
Membrane scission | vps20, snf7 and vps24 | 67 |
Arp2/3, actin-related protein 2/3; GUV, giant unilamellar vesicle; ICAM1, intercellular adhesion molecule 1; MHC, major histocompatibility complex; NPF, nucleation-promotion factor; N-WASP, neuronal-Wiscott–Aldrich syndrome protein (also known as WASL); PtdIns(4,5)P2, phosphatidylinositol-4,5-bisphosphate; snf7, sucrose non-fermenting protein 7; Vps, vacuole protein sorting protein.