Literature DB >> 26929357

Role of bacteriophage T4 baseplate in regulating assembly and infection.

Moh Lan Yap1, Thomas Klose1, Fumio Arisaka2, Jeffrey A Speir3, David Veesler4, Andrei Fokine1, Michael G Rossmann5.   

Abstract

Bacteriophage T4 consists of a head for protecting its genome and a sheathed tail for inserting its genome into a host. The tail terminates with a multiprotein baseplate that changes its conformation from a "high-energy" dome-shaped to a "low-energy" star-shaped structure during infection. Although these two structures represent different minima in the total energy landscape of the baseplate assembly, as the dome-shaped structure readily changes to the star-shaped structure when the virus infects a host bacterium, the dome-shaped structure must have more energy than the star-shaped structure. Here we describe the electron microscopy structure of a 3.3-MDa in vitro-assembled star-shaped baseplate with a resolution of 3.8 Å. This structure, together with other genetic and structural data, shows why the high-energy baseplate is formed in the presence of the central hub and how the baseplate changes to the low-energy structure, via two steps during infection. Thus, the presence of the central hub is required to initiate the assembly of metastable, high-energy structures. If the high-energy structure is formed and stabilized faster than the low-energy structure, there will be insufficient components to assemble the low-energy structure.

Entities:  

Keywords:  bacteriophage T4; baseplate assembly; conformational changes; cryo-EM reconstruction; near-atomic resolution

Mesh:

Substances:

Year:  2016        PMID: 26929357      PMCID: PMC4791028          DOI: 10.1073/pnas.1601654113

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  45 in total

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7.  Time-resolved DNA release from an O-antigen-specific Salmonella bacteriophage with a contractile tail.

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