ESCRT-III polymers in membrane neck constriction

Trends in Cell Biology

Volumn 22, Issue 3, 2012, Pages 133-140

  Guizetti, Julien ^a   Gerlich, Daniel W ^a  

^a ETH ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOSOMAL SORTING COMPLEX REQUIRED FOR TRANSPORT III; ESCRT PROTEIN; MEMBRANE PROTEIN; POLYMER; UNCLASSIFIED DRUG;

AUTOPHAGY; CELL DIVISION; CELL MIGRATION; CELL STRUCTURE; CRYSTAL STRUCTURE; CYTOKINESIS; CYTOPLASM; CYTOSOL; ENDOCYTOSIS; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS; IN VITRO STUDY; IN VIVO STUDY; LIPID METABOLISM; MEMBRANE BIOLOGY; MICROTUBULE; MODEL; NONHUMAN; POLYMERIZATION; PRIORITY JOURNAL; PROTEIN HOMEOSTASIS; PROTEIN STABILITY; PROTEIN STRUCTURE; REVIEW; VIRUS RELEASE;

ANIMALS; CELL MEMBRANE; CYTOPLASM; ENDOSOMAL SORTING COMPLEXES REQUIRED FOR TRANSPORT; HUMANS; PROTEIN MULTIMERIZATION; PROTEIN SUBUNITS;

EID: 84857783323     PISSN: 09628924     EISSN: 18793088     Source Type: Journal    
DOI: 10.1016/j.tcb.2011.11.007     Document Type: Review

References (67)

1. Stuffers S., et al. Multivesicular endosome biogenesis in the absence of ESCRTs. Traffic 2009, 10:925-937.
2. Ewers H., Helenius A. Lipid-mediated endocytosis. Cold Spring Harb. Perspect. Biol. 2011, 3:a004721.
3. Matsuo H., et al. Role of LBPA and Alix in multivesicular liposome formation and endosome organization. Science 2004, 303:531-534.
4. Hurley J.H., et al. Membrane budding. Cell 2010, 143:875-887.
5. Babst M. MVB vesicle formation: ESCRT-dependent, ESCRT-independent and everything in between. Curr. Opin. Cell Biol. 2011, 23:452-457.
6. Weiss E.R., Gottlinger H. The role of cellular factors in promoting HIV budding. J. Mol. Biol. 2011, 410:525-533.
7. Ramachandran R. Vesicle scission: dynamin. Semin. Cell Dev. Biol. 2011, 22:10-17.
8. Roux A., et al. GTP-dependent twisting of dynamin implicates constriction and tension in membrane fission. Nature 2006, 441:528-531.
9. Henne W.M., et al. The ESCRT pathway. Dev. Cell 2011, 21:77-91.
10. Hurley J.H., Emr S.D. The ESCRT complexes: structure and mechanism of a membrane-trafficking network. Annu. Rev. Biophys. Biomol. Struct. 2006, 35:277-298.
11. Raiborg C., Stenmark H. The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins. Nature 2009, 458:445-452.
12. Hanson P.I., et al. Cell biology of the ESCRT machinery. Curr. Opin. Cell Biol. 2009, 21:568-574.
13. Williams R.L., Urbe S. The emerging shape of the ESCRT machinery. Nat. Rev. Mol. Cell Biol. 2007, 8:355-368.
14. Slagsvold T., et al. Endosomal and non-endosomal functions of ESCRT proteins. Trends Cell Biol. 2006, 16:317-326.
15. Carlton J.G., Martin-Serrano J. Parallels between cytokinesis and retroviral budding: a role for the ESCRT machinery. Science 2007, 316:1908-1912.
16. Morita E., et al. Human ESCRT-III and VPS4 proteins are required for centrosome and spindle maintenance. Proc. Natl. Acad. Sci. U. S. A. 2010, 107:12889-12894.
17. Elia N., et al. Dynamics of endosomal sorting complex required for transport (ESCRT) machinery during cytokinesis and its role in abscission. Proc. Natl. Acad. Sci. U. S. A. 2011, 108:4846-4851.
18. Guizetti J., et al. Cortical constriction during abscission involves helices of ESCRT-III-dependent filaments. Science 2011, 331:1616-1620.
19. Morita E., et al. Human ESCRT and ALIX proteins interact with proteins of the midbody and function in cytokinesis. EMBO J. 2007, 26:4215-4227.
20. Lee J.A., et al. ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration. Curr. Biol. 2007, 17:1561-1567.
21. Rusten T.E., Stenmark H. How do ESCRT proteins control autophagy?. J. Cell Sci. 2009, 122:2179-2183.
22. Martin-Serrano J., Neil S.J. Host factors involved in retroviral budding and release. Nat. Rev. Microbiol. 2011, 9:519-531.
23. Morita E., Sundquist W.I. Retrovirus budding. Annu. Rev. Cell Dev. Biol. 2004, 20:395-425.
24. Lata S., et al. Structure and function of ESCRT-III. Biochem. Soc. Trans. 2009, 37:156-160.
25. Wollert T., et al. Membrane scission by the ESCRT-III complex. Nature 2009, 458:172-177.
26. Ghazi-Tabatabai S., et al. Structure and disassembly of filaments formed by the ESCRT-III subunit Vps24. Structure 2008, 16:1345-1356.
27. Wollert T., Hurley J.H. Molecular mechanism of multivesicular body biogenesis by ESCRT complexes. Nature 2010, 464:864-869.
28. Pires R., et al. A crescent-shaped ALIX dimer targets ESCRT-III CHMP4 filaments. Structure 2009, 17:843-856.
29. Saksena S., et al. Functional reconstitution of ESCRT-III assembly and disassembly. Cell 2009, 136:97-109.
30. Fyfe I., et al. Association of ESCRT-II with VPS20 generates a curvature sensitive protein complex capable of nucleating filaments of ESCRT-III. J. Biol. Chem. 2011, 286:34262-34270.
31. Hurley J.H., Hanson P.I. Membrane budding and scission by the ESCRT machinery: it's all in the neck. Nat. Rev. Mol. Cell Biol. 2010, 11:556-566.
32. Ganser-Pornillos B.K., et al. The structural biology of HIV assembly. Curr. Opin. Struct. Biol. 2008, 18:203-217.
33. von Schwedler U.K., et al. The protein network of HIV budding. Cell 2003, 114:701-713.
34. Morita E., et al. ESCRT-III protein requirements for HIV-1 budding. Cell Host Microbe 2011, 9:235-242.
35. Baumgartel V., et al. Live-cell visualization of dynamics of HIV budding site interactions with an ESCRT component. Nat. Cell Biol. 2011, 13:469-474.
36. Jouvenet N., et al. Dynamics of ESCRT protein recruitment during retroviral assembly. Nat. Cell Biol. 2011, 13:394-401.
37. Teis D., et al. ESCRT-II coordinates the assembly of ESCRT-III filaments for cargo sorting and multivesicular body vesicle formation. EMBO J. 2010, 29:871-883.
38. Barr F.A., Gruneberg U. Cytokinesis: placing and making the final cut. Cell 2007, 131:847-860.
39. Guizetti J., Gerlich D.W. Cytokinetic abscission in animal cells. Semin. Cell Dev. Biol. 2010, 21:909-916.
40. Steigemann P., Gerlich D.W. Cytokinetic abscission: cellular dynamics at the midbody. Trends Cell Biol. 2009, 19:606-616.
41. Eggert U.S., et al. Animal cytokinesis: from parts list to mechanisms. Annu. Rev. Biochem. 2006, 75:543-566.
42. Carlton J.G., et al. Differential requirements for Alix and ESCRT-III in cytokinesis and HIV-1 release. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:10541-10546.
43. Leung K.F., et al. Evolution of the multivesicular body ESCRT machinery; retention across the eukaryotic lineage. Traffic 2008, 9:1698-1716.
44. Samson R.Y., et al. A role for the ESCRT system in cell division in archaea. Science 2008, 322:1710-1713.
45. Lindas A.C., et al. A unique cell division machinery in the Archaea. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:18942-18946.
46. Shim S., et al. Structure/function analysis of four core ESCRT-III proteins reveals common regulatory role for extreme C-terminal domain. Traffic 2007, 8:1068-1079.
47. Babst M., et al. ESCRT-III: an endosome-associated heterooligomeric protein complex required for MVB sorting. Dev. Cell 2002, 3:271-282.
48. Muziol T., et al. Structural basis for budding by the ESCRT-III factor CHMP3. Dev. Cell 2006, 10:821-830.
49. Lata S., et al. Helical structures of ESCRT-III are disassembled by VPS4. Science 2008, 321:1354-1357.
50. Hanson P.I., et al. Plasma membrane deformation by circular arrays of ESCRT-III protein filaments. J. Cell Biol. 2008, 180:389-402.
51. Bodon G., et al. Charged multivesicular body protein 2B (CHMP2B) of the endosomal sorting complex required for transport-III (ESCRT-III) polymerizes into helical structures deforming the plasma membrane. J. Biol. Chem. 2011, 286:40276-40286.
52. Lata S., et al. Structural basis for autoinhibition of ESCRT-III CHMP3. J. Mol. Biol. 2008, 378:818-827.
53. Zamborlini A., et al. Release of autoinhibition converts ESCRT-III components into potent inhibitors of HIV-1 budding. Proc. Natl. Acad. Sci. U. S. A. 2006, 103:19140-19145.
54. Bajorek M., et al. Structural basis for ESCRT-III protein autoinhibition. Nat. Struct. Mol. Biol. 2009, 16:754-762.
55. Teis D., et al. Ordered assembly of the ESCRT-III complex on endosomes is required to sequester cargo during MVB formation. Dev. Cell 2008, 15:578-589.
56. Malerod L., Stenmark H. ESCRTing membrane deformation. Cell 2009, 136:15-17.
57. Babst M., et al. The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function. EMBO J. 1998, 17:2982-2993.
58. Toomre D., Bewersdorf J. A new wave of cellular imaging. Annu. Rev. Cell Dev. Biol. 2010, 26:285-314.
59. Shu X., et al. A genetically encoded tag for correlated light and electron microscopy of intact cells, tissues, and organisms. PLoS Biol. 2011, 9:e1001041.
60. Lippincott-Schwartz J., et al. Photobleaching and photoactivation: following protein dynamics in living cells. Nat. Cell Biol. 2003, (Suppl.):S7-S14.
61. Kozlovsky Y., Kozlov M.M. Membrane fission: model for intermediate structures. Biophys. J. 2003, 85:85-96.
62. Roll-Mecak A., Vale R.D. Structural basis of microtubule severing by the hereditary spastic paraplegia protein spastin. Nature 2008, 451:363-367.
63. Trajkovic K., et al. Ceramide triggers budding of exosome vesicles into multivesicular endosomes. Science 2008, 319:1244-1247.
64. Mobius W., et al. Recycling compartments and the internal vesicles of multivesicular bodies harbor most of the cholesterol found in the endocytic pathway. Traffic 2003, 4:222-231.
65. Sagona A.P., et al. PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody. Nat. Cell Biol. 2010, 12:362-371.
66. Liu J., et al. Endocytic vesicle scission by lipid phase boundary forces. Proc. Natl. Acad. Sci. U. S. A. 2006, 103:10277-10282.
67. Fabrikant G., et al. Computational model of membrane fission catalyzed by ESCRT-III. PLoS Comput. Biol. 2009, 5:e1000575.