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Bacterial Cytoskeletal Elements Establishment of morphogenesis in bacteria ? ? Cytoskeletal elements The bacterial cytoskeleton Eukaryotes tubulin actin IFs Bacteria FtsZ MreB Ccrp (Crescentin) 3D structures of cytoskeletal elements Phylogeny of FtsZ Tubulin ortholog FtsZ forms a ring-like structure in the cell centre Immuno-fluorescence of FtsZ (red) and DNA (green) in Bacillus subtilis E. coli: FtsZ-GFP Tubulin forms hollow tubules, while FtsZ forms single strand polymers Assembly of the divisome Cell division in Bacillus subtilis Actin Treadmilling Plasmid segregation via a double protein filament K. Gerdes, J. Pogliano Bipolar movement through search and capturing of a second plasmid ParM-Alexa 488, ParR-Alexa red D. Mullins Structures of actin-like proteins F-actin and MreB filaments MreB MreB ParM ParM MreB J. Löwe Depletion of MreB (or MreC) leads to the formation of round cells and is lethal 2 4 6 doubling times membrane-stain The depletion of MreB leads to a loss in rod- shaped cell morphology GFP-MreB: dynamc helical filaments? GFP-MreB 2D arrangement of MreB filaments 3D arrangement of MreB filaments Filament dynamics at 100 nm resolution: TIRF-SIM YFP-MreB N-SIM A. Rohrbach Model for the generation of rod shape Intermediate-Filament proteins Crescentin affects cell curvature in Caulobacter crescentus C. Jacobs-Wagner, Yale Crescentin localizes to the short axis of the cell Crescentin forms left handed helices Crescentin-YFP Deletion of IF encoding genes leads to loss of cell shape in Helicobacter pylori Ccrps (coiled coil-rich proteins) form long bundles of filaments Cell curvature through mechanical bending of cells via a rigid protein filament Positioning of magnetosomes through an actin-like protein (MamK) Spiroplasma melliferum Bacterial cytoskeletal elements Model for the function of MreB Motility of Spiroplasma Filament formation in a mammalian cell system YFP-MreB CFP-Mbl mCherry-MreBH .

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The Cytoskeleton in Cell-Autonomous Immunity: Structural Determinants of Host Defence
Mostowy & Shenoy, Nat Rev Immunol, doi:10.1038/nri3877 The cytoskeleton in cell-autonomous immunity: structural determinants of host defence Serge Mostowy and Avinash R. Shenoy Medical Research Council Centre of Molecular Bacteriology and Infection (CMBI), Imperial College London, Armstrong Road, London SW7 2AZ, UK. e‑mails: [email protected] ; [email protected] doi:10.1038/nri3877 Published online 21 August 2015 Abstract Host cells use antimicrobial proteins, pathogen-restrictive compartmentalization and cell death in their defence against intracellular pathogens. Recent work has revealed that four components of the cytoskeleton — actin, microtubules, intermediate filaments and septins, which are well known for their roles in cell division, shape and movement — have important functions in innate immunity and cellular self-defence. Investigations using cellular and animal models have shown that these cytoskeletal proteins are crucial for sensing bacteria and for mobilizing effector mechanisms to eliminate them. In this Review, we highlight the emerging roles of the cytoskeleton as a structural determinant of cell-autonomous host defence. 1 Mostowy & Shenoy, Nat Rev Immunol, doi:10.1038/nri3877 Cell-autonomous immunity, which is defined as the ability of a host cell to eliminate an invasive infectious agent, is a first line of defence against microbial pathogens 1 . It relies on antimicrobial proteins, specialized degradative compartments and programmed host cell death 1–3 . Cell- autonomous immunity is mediated by tiered innate immune signalling networks that sense microbial pathogens and stimulate downstream pathogen elimination programmes. Recent studies on host– microorganism interactions show that components of the host cell cytoskeleton are integral to the detection of bacterial pathogens as well as to the mobilization of antibacterial responses (FIG.
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Soft Matter PAPER
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A Metabolic Assembly Line in Bacteria
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Of the Bacterial Cytoskeleton
30 Apr 2004 18:9 AR AR214-BB33-09.tex AR214-BB33-09.sgm LaTeX2e(2002/01/18) P1: FHD 10.1146/annurev.biophys.33.110502.132647 Annu. Rev. Biophys. Biomol. Struct. 2004. 33:177–98 doi: 10.1146/annurev.biophys.33.110502.132647 Copyright c 2004 by Annual Reviews. All rights reserved First published online as a Review in Advance on January 7, 2004 MOLECULES OF THE BACTERIAL CYTOSKELETON Jan Lowe,¨ Fusinita van den Ent, and Linda A. Amos MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 2QH, United Kingdom; email: [email protected]; [email protected]; [email protected] Key Words FtsZ, MreB, ParM, tubulin, actin ■ Abstract The structural elucidation of clear but distant homologs of actin and tubulin in bacteria and GFP labeling of these proteins promises to reinvigorate the field of prokaryotic cell biology. FtsZ (the tubulin homolog) and MreB/ParM (the actin ho- mologs) are indispensable for cellular tasks that require the cell to accurately position molecules, similar to the function of the eukaryotic cytoskeleton. FtsZ is the organizing molecule of bacterial cell division and forms a filamentous ring around the middle of the cell. Many molecules, including MinCDE, SulA, ZipA, and FtsA, assist with this process directly. Recently, genes much more similar to tubulin than to FtsZ have been identified in Verrucomicrobia. MreB forms helices underneath the inner membrane and probably defines the shape of the cell by positioning transmembrane and periplas- mic cell wall–synthesizing enzymes. Currently, no interacting proteins are known for MreB and its relatives that help these proteins polymerize or depolymerize at certain times and places inside the cell.
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Arxiv:1105.2423V1 [Physics.Bio-Ph] 12 May 2011 C
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Cytoskeleton and Cell Motility Thomas Risler To cite this version: Thomas Risler. Cytoskeleton and Cell Motility. Robert A. Meyers. Encyclopedia of Complexity and System Science, Springer, pp.1738-1774, 2009, 978-0-387-75888-6. 10.1007/978-0-387-30440-3_112. hal-00961037 HAL Id: hal-00961037 https://hal.archives-ouvertes.fr/hal-00961037 Submitted on 22 Mar 2017 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Cytoskeleton and Cell Motility Thomas Risler Institut Curie, Centre de Recherche, UMR 168 (UPMC Univ Paris 06, CNRS), 26 rue d'Ulm, F-75005 Paris, France Article Outline C. Macroscopic phenomenological approaches: The active gels Glossary D. Comparisons of the diﬀerent approaches to de- scribing active polymer solutions I. Deﬁnition of the Subject and Its Importance VIII. Extensions and Future Directions II. Introduction Acknowledgments III. The Diversity of Cell Motility Bibliography A. Swimming B. Crawling C. Extensions of cell motility IV. The Cell Cytoskeleton A. Biopolymers B. Molecular motors C. Motor families D. Other cytoskeleton-associated proteins E. Cell anchoring and regulatory pathways F. The prokaryotic cytoskeleton V. Filament-Driven Motility A. Microtubule growth and catastrophes B.
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