Literature DB >> 16116440

The tail structure of bacteriophage T4 and its mechanism of contraction.

Victor A Kostyuchenko1, Paul R Chipman, Petr G Leiman, Fumio Arisaka, Vadim V Mesyanzhinov, Michael G Rossmann.   

Abstract

Bacteriophage T4 and related viruses have a contractile tail that serves as an efficient mechanical device for infecting bacteria. A three-dimensional cryo-EM reconstruction of the mature T4 tail assembly at 15-A resolution shows the hexagonal dome-shaped baseplate, the extended contractile sheath, the long tail fibers attached to the baseplate and the collar formed by six whiskers that interact with the long tail fibers. Comparison with the structure of the contracted tail shows that tail contraction is associated with a substantial rearrangement of the domains within the sheath protein and results in shortening of the sheath to about one-third of its original length. During contraction, the tail tube extends beneath the baseplate by about one-half of its total length and rotates by 345 degrees , allowing it to cross the host's periplasmic space.

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Year:  2005        PMID: 16116440     DOI: 10.1038/nsmb975

Source DB:  PubMed          Journal:  Nat Struct Mol Biol        ISSN: 1545-9985            Impact factor:   15.369


  81 in total

1.  Structure of the three N-terminal immunoglobulin domains of the highly immunogenic outer capsid protein from a T4-like bacteriophage.

Authors:  Andrei Fokine; Mohammad Z Islam; Zhihong Zhang; Valorie D Bowman; Venigalla B Rao; Michael G Rossmann
Journal:  J Virol       Date:  2011-06-01       Impact factor: 5.103

Review 2.  Structural biology of type VI secretion systems.

Authors:  Eric Cascales; Christian Cambillau
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2012-04-19       Impact factor: 6.237

3.  Structure of lactococcal phage p2 baseplate and its mechanism of activation.

Authors:  Giuliano Sciara; Cecilia Bebeacua; Patrick Bron; Denise Tremblay; Miguel Ortiz-Lombardia; Julie Lichière; Marin van Heel; Valérie Campanacci; Sylvain Moineau; Christian Cambillau
Journal:  Proc Natl Acad Sci U S A       Date:  2010-03-29       Impact factor: 11.205

4.  Structure of the bacteriophage T4 long tail fiber receptor-binding tip.

Authors:  Sergio G Bartual; José M Otero; Carmela Garcia-Doval; Antonio L Llamas-Saiz; Richard Kahn; Gavin C Fox; Mark J van Raaij
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-01       Impact factor: 11.205

5.  How the phage T4 injection machinery works including energetics, forces, and dynamic pathway.

Authors:  Ameneh Maghsoodi; Anupam Chatterjee; Ioan Andricioaei; Noel C Perkins
Journal:  Proc Natl Acad Sci U S A       Date:  2019-11-25       Impact factor: 11.205

6.  Structure of the type VI secretion system contractile sheath.

Authors:  Mikhail Kudryashev; Ray Yu-Ruei Wang; Maximilian Brackmann; Sebastian Scherer; Timm Maier; David Baker; Frank DiMaio; Henning Stahlberg; Edward H Egelman; Marek Basler
Journal:  Cell       Date:  2015-02-26       Impact factor: 41.582

7.  Anatomy of a lactococcal phage tail.

Authors:  Stephen Mc Grath; Horst Neve; Jos F M L Seegers; Robyn Eijlander; Christina S Vegge; Lone Brøndsted; Knut J Heller; Gerald F Fitzgerald; Finn K Vogensen; Douwe van Sinderen
Journal:  J Bacteriol       Date:  2006-06       Impact factor: 3.490

8.  Structure and transformation of bacteriophage A511 baseplate and tail upon infection of Listeria cells.

Authors:  Ricardo C Guerrero-Ferreira; Mario Hupfeld; Sergey Nazarov; Nicholas Mi Taylor; Mikhail M Shneider; Jagan M Obbineni; Martin J Loessner; Takashi Ishikawa; Jochen Klumpp; Petr G Leiman
Journal:  EMBO J       Date:  2019-01-02       Impact factor: 11.598

Review 9.  Protein interactions in the assembly of the tail of bacteriophage T4.

Authors:  Fumio Arisaka; Shuji Kanamaru
Journal:  Biophys Rev       Date:  2013-04-24

10.  Common Evolutionary Origin of Procapsid Proteases, Phage Tail Tubes, and Tubes of Bacterial Type VI Secretion Systems.

Authors:  Andrei Fokine; Michael G Rossmann
Journal:  Structure       Date:  2016-09-22       Impact factor: 5.006

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