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Bacteriophage PRD1 shares many structural and functional similarities with adenovirus. A major difference is the PRD1 internal membrane, which acts in concert with vertex proteins to translocate the phage genome into the host. Multiresolution models of the PRD1 capsid, together with genetic analyses, provide fine details of the molecular interactions associated with particle stability and membrane dynamics. The N- and C-termini of the major coat protein (P3), which are required for capsid assembly, act as conformational switches bridging capsid to membrane and linking P3 trimers. Electrostatic P3-membrane interactions increase virion stability upon DNA packaging. Newly revealed proteins suggest how the metastable vertex works and how the capsid edges are stabilized.

Original publication

DOI

10.1038/nsb837

Type

Journal article

Journal

Nat Struct Biol

Publication Date

10/2002

Volume

9

Pages

756 - 763

Keywords

Bacteriophage PRD1, Capsid, Cloning, Molecular, Crystallography, X-Ray, Intracellular Membranes, Models, Molecular