Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography
Pore formation in membranes is important for mammalian immune defense against invading bacteria. Induced by complement activation, the membrane attack complex (MAC) forms through sequential binding and membrane insertion of C5b6, C7, C8, and C9. Using cryo-electron tomography with a Volta phase plat...
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doaj-5e952d1a7c884b60846268471c6cd54c2020-11-25T02:20:56ZengElsevierCell Reports2211-12472016-04-011511810.1016/j.celrep.2016.03.002Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron TomographyThomas H. Sharp0Abraham J. Koster1Piet Gros2Section Electron Microscopy, Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, the NetherlandsSection Electron Microscopy, Department of Molecular Cell Biology, Leiden University Medical Center, 2300 RC Leiden, the NetherlandsCrystal and Structural Chemistry, Bijvoet Center for Biomolecular Research and Department of Chemistry, Faculty of Science, Utrecht University, Padualaan 8, 3584 CH Utrecht, the NetherlandsPore formation in membranes is important for mammalian immune defense against invading bacteria. Induced by complement activation, the membrane attack complex (MAC) forms through sequential binding and membrane insertion of C5b6, C7, C8, and C9. Using cryo-electron tomography with a Volta phase plate and subtomogram averaging, we imaged C5b-7, C5b-8, and C5b-9 complexes and determined the C5b-9 pore structure in lipid bilayers. The in situ C5b-9 pore structure at 2.3-nm resolution reveals a 10- to 11.5-nm cone-shaped pore starting with C5b678 and multiple copies of C9 that is poorly closed, yielding a seam between C9 and C6 substituting for the shorter β strands in C6 and C7. However, large variations of composite pore complexes are apparent in subtomograms. Oligomerized initiator complexes C5b-7 and C5b-8 show stages of membrane binding, deformation, and perforation that yield ∼3.5-nm-wide pores. These data indicate a dynamic process of pore formation that likely adapts to biological membranes under attack.http://www.sciencedirect.com/science/article/pii/S2211124716302261phase platemembrane attack complexcomplementelectron tomographysubtomogram averagemembrane pore |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas H. Sharp Abraham J. Koster Piet Gros |
spellingShingle |
Thomas H. Sharp Abraham J. Koster Piet Gros Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography Cell Reports phase plate membrane attack complex complement electron tomography subtomogram average membrane pore |
author_facet |
Thomas H. Sharp Abraham J. Koster Piet Gros |
author_sort |
Thomas H. Sharp |
title |
Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography |
title_short |
Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography |
title_full |
Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography |
title_fullStr |
Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography |
title_full_unstemmed |
Heterogeneous MAC Initiator and Pore Structures in a Lipid Bilayer by Phase-Plate Cryo-electron Tomography |
title_sort |
heterogeneous mac initiator and pore structures in a lipid bilayer by phase-plate cryo-electron tomography |
publisher |
Elsevier |
series |
Cell Reports |
issn |
2211-1247 |
publishDate |
2016-04-01 |
description |
Pore formation in membranes is important for mammalian immune defense against invading bacteria. Induced by complement activation, the membrane attack complex (MAC) forms through sequential binding and membrane insertion of C5b6, C7, C8, and C9. Using cryo-electron tomography with a Volta phase plate and subtomogram averaging, we imaged C5b-7, C5b-8, and C5b-9 complexes and determined the C5b-9 pore structure in lipid bilayers. The in situ C5b-9 pore structure at 2.3-nm resolution reveals a 10- to 11.5-nm cone-shaped pore starting with C5b678 and multiple copies of C9 that is poorly closed, yielding a seam between C9 and C6 substituting for the shorter β strands in C6 and C7. However, large variations of composite pore complexes are apparent in subtomograms. Oligomerized initiator complexes C5b-7 and C5b-8 show stages of membrane binding, deformation, and perforation that yield ∼3.5-nm-wide pores. These data indicate a dynamic process of pore formation that likely adapts to biological membranes under attack. |
topic |
phase plate membrane attack complex complement electron tomography subtomogram average membrane pore |
url |
http://www.sciencedirect.com/science/article/pii/S2211124716302261 |
work_keys_str_mv |
AT thomashsharp heterogeneousmacinitiatorandporestructuresinalipidbilayerbyphaseplatecryoelectrontomography AT abrahamjkoster heterogeneousmacinitiatorandporestructuresinalipidbilayerbyphaseplatecryoelectrontomography AT pietgros heterogeneousmacinitiatorandporestructuresinalipidbilayerbyphaseplatecryoelectrontomography |
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