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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Main Authors: Thomas H. Sharp, Abraham J. Koster, Piet Gros
Format: Article
Language:English
Published: Elsevier 2016-04-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124716302261
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spelling 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
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AT abrahamjkoster heterogeneousmacinitiatorandporestructuresinalipidbilayerbyphaseplatecryoelectrontomography
AT pietgros heterogeneousmacinitiatorandporestructuresinalipidbilayerbyphaseplatecryoelectrontomography
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