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      Structural Basis of Vesicle Formation at the Inner Nuclear Membrane

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          Summary

          Vesicular nucleo-cytoplasmic transport is becoming recognized as a general cellular mechanism for translocation of large cargoes across the nuclear envelope. Cargo is recruited, enveloped at the inner nuclear membrane (INM), and delivered by membrane fusion at the outer nuclear membrane. To understand the structural underpinning for this trafficking, we investigated nuclear egress of progeny herpesvirus capsids where capsid envelopment is mediated by two viral proteins, forming the nuclear egress complex (NEC). Using a multi-modal imaging approach, we visualized the NEC in situ forming coated vesicles of defined size. Cellular electron cryo-tomography revealed a protein layer showing two distinct hexagonal lattices at its membrane-proximal and membrane-distant faces, respectively. NEC coat architecture was determined by combining this information with integrative modeling using small-angle X-ray scattering data. The molecular arrangement of the NEC establishes the basic mechanism for budding and scission of tailored vesicles at the INM.

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          Highlights

          • Multimodal imaging reveals mechanism of vesicle formation at inner nuclear membrane

          • Nucleo-cytoplasmic cargo vesicle coat in situ comprises two distinct lattices

          • Lattices are formed by hexameric building blocks made of the nuclear egress complex

          • Induction of membrane curvature based solely on heterodimeric interactions

          Abstract

          A multi-modal live-cell and cryo-imaging approach reveals how vesicles assemble at the inner nuclear membrane for transport to the cytoplasm during herpesvirus maturation. This also suggests a functional model for counterparts in uninfected cells that mediate nuclear egress of large cargo like ribonucleoprotein particles.

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          Most cited references37

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          Nuclear pore complex is able to transport macromolecules with diameters of about 39 nm.

          Bidirectional transport of macromolecules between the nucleus and the cytoplasm occurs through the nuclear pore complexes (NPCs) by a signal-mediated mechanism that is directed by targeting signals (NLSs) residing on the transported molecules or "cargoes." Nuclear transport starts after interaction of the targeting signal with soluble cellular receptors. After the formation of the cargo-receptor complex in the cytosol, this complex crosses the NPC. Herein, we use gold particles of various sizes coated with cargo-receptor complexes to determine precisely how large macromolecules crossing the NPC by the signal-mediated transport mechanism could be. We found that cargo-receptor-gold complexes with diameter close to 39 nm could be translocated by the NPC. This implies that macromolecules much larger than the assumed functional NPC diameter of 26 nm can be transported into the karyoplasm. The physiological relevance of this finding was supported by the observation that intact nucleocapsids of human hepatitis B virus with diameters of 32 and 36 nm are able to cross the nuclear pore without disassembly.
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            Focused-ion-beam thinning of frozen-hydrated biological specimens for cryo-electron microscopy.

            Cryo-electron microscopy can provide high-resolution structural information about cells and organelles in the nearly native, frozen-hydrated state. Applicability, however, is limited by difficulties encountered in preparing suitably thin, vitreously frozen biological specimens. We demonstrate, by cryo-electron tomography of Escherichia coli cells, that a focused ion beam (FIB) can be used to thin whole frozen-hydrated cells in a convenient and essentially artifact-free way.
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              Coat proteins and vesicle budding.

              The trafficking of proteins within eukaryotic cells is achieved by the capture of cargo and targeting molecules into vesicles that bud from a donor membrane and deliver their contents to a receiving department. This process is bidirectional and may involve multiple organelles within a cell. Distinct coat proteins mediate each budding event, serving both to shape the transport vesicle and to select by direct or indirect interaction the desired set of cargo molecules. Secretion, which has been viewed as a default pathway, may require sorting and packaging signals on transported molecules to ensure their rapid delivery to the cell surface.
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                Author and article information

                Contributors
                Journal
                Cell
                Cell
                Cell
                Cell Press
                0092-8674
                1097-4172
                17 December 2015
                17 December 2015
                : 163
                : 7
                : 1692-1701
                Affiliations
                [1 ]Oxford Particle Imaging Centre, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK
                [2 ]Diamond Light Source Ltd., Harwell Science and Innovation Campus, Didcot OX11 0DE, UK
                [3 ]Department of Molecular Biology, Princeton Neuroscience Institute, Princeton University, Washington Road, Princeton, NJ 08544, USA
                [4 ]Institute of Molecular Virology and Cell Biology, Friedrich-Loeffler-Institut, 17493 Greifswald-Insel Riems, Germany
                [5 ]Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, Am Klopferspitz 18, 82152 Martinsried, Germany
                [6 ]Helmholtz Zentrum Berlin für Materialien und Energie GmbH, Wilhelm-Conrad-Röntgen Campus, 12489 Berlin, Germany
                [7 ]Micron Oxford, Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK
                [8 ]Max von Pettenkofer-Institut, Ludwig-Maximilians-Universität München, Pettenkoferstr. 9a, 80336 Munich, Germany
                Author notes
                []Corresponding author thomas.mettenleiter@ 123456fli.bund.de
                [∗∗ ]Corresponding author kay@ 123456strubi.ox.ac.uk
                [9]

                Co-first author

                [10]

                Present address: Heinrich-Pette-Institute, Leibniz-Institute of Experimental Virology, Martinistrasse 52, 20251 Hamburg, Germany

                [11]

                Present address: Paul Scherrer Institut, Swiss Light Source, 5232 Villigen PSI, Switzerland

                Article
                S0092-8674(15)01548-2
                10.1016/j.cell.2015.11.029
                4701712
                26687357
                93174dbe-5893-42b9-9615-83ebb0a4491a
                © 2015 The Authors

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 1 June 2015
                : 11 September 2015
                : 6 November 2015
                Categories
                Article

                Cell biology
                Cell biology

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