Viral architecture
Transcription
Viral architecture
Viral architecture Functions of the virus particle = virion: Genome protection (coating) Receptor recognition and penetration into host cell Genome uncoating and targeting Incorporation of enzymes (e.g., retroviruses) An insight to the virion structure from a novelist… …and the viral entities hidden within, submicroscopic parasites in their soviet socialist protein coats. Don DeLillo “UNDERWORLD” Principles of virion organization Most virions resemble nuts with a genome inside and a protective protein shell outside Small genome size dictates repeated use of a small number of building blocks (protein subunits) Self-organization of repeated subunits results in symmetrical structures Virion shape is determined by interactions between protein subunits Helical symmetry results in elongated virions Helical capsid architecture Organization of the protein subunits (yellow) and RNA (red) in a helical capsid Beet yellows virus, a 1,400 x 12 nm flexuous filament Tobacco mosaic virus, a 300 x 18 nm rod Structure of the TMV capsid protein Self-assembly of the TMV virion Icosahedral symmetry results in roughly spherical virions Virus proteins (VPs) 1, 2, and 3 share β-barrel fold Poliovirus, a 30 nm sphere Structure of the icosahedral capsids 3-D structure of the capsid protein Quasi-equivalent arrangement of the identical protein subunits in a capsid Nodamura virus Insect-infecting (+)RNA virus Cryoelectron microscopy Polio 32 nm Adeno 110 nm Papilloma 60 nm Herpes 125 nm Spherical RNA or DNA viruses that infect bacteria, fungi, plants, and animals often share the similar, β-barrel type of a capsid protein subunit(s) Self-assembly of the simple, icosahedral virions Assembly of the large icosahedral capsids requires scaffolding proteins, which are removed prior to DNA packaging scaffold DNA within herpesvirus capsid Helical, icosahedral, or combined virions can be complex Geminivirus (ssDNA within a double sphere) Atomic force microscopy used to visualize tails of the closterovirus (ssRNA + four proteins) Tailed bacteriophages (dsDNA packed in heads): T4, T4, P2 Acquisition of a viral envelope viral envelope protein (transmembrane) nucleocapsid assembly Viral genome (RNA or DNA) capsid protein mature progeny virion lipid bilayer Surface of Herpes simplex virus modeled using cryoelectron tomography Glycoprotein Membrane Structure of Herpes simplex virus Glycoprotein Membrane Tegument protein Nucleocapsid Protein-only capsids Icosahedral Helical JRC Picornavirus SF Microviridae Bromoviridae Polyomaviridae Adjoining Tymoviridae Papillomaviridae icosahedra Tombusviridae Parvoviridae Geminiviridae Ourmiaviridae Circoviridae (JRC?) Birnaviridae Concentric icosahedra JRC-DB Reoviridae Adenoviridae (JRC/non-JRC) Other folds Leviviridae Picobirnaviridae Totiviridae Partitiviridae Closteroviridae Flexiviridae Virgaviridae Potyviridae Inoviridae Rudiviridae Unknown folds Caulimoviridae Chrysoviridae Complex Spindle-shaped Bicaudoviridae Tailed bacteriophages and archaeal viruses Caudovirales, GTA Capsid-less Viroids Narnaviridae Hypoviridae Endornaviridae Membrane-containing virions Inner membrane Isosahedral capsid; JRC-DB Corticoviridae, Tectiviridae STIV NCLDV: Outer membrane Isosahedral Concentric icosahedra Cystoviridae Phycodnaviridae, Mimiviridae Arterivirida Flaviviridae Hepadnaviridae Togaviridae Herpesvirales Double membrane NCLDV Asfaviridae Ascoviridae Iridoviridae Polydnaviridae Brick-shaped Poxviridae (NCLDV) Droplet-shaped Fuselloviridae Guttaviridae Bottle-shaped Ampullaviridae Pleomorphic virions, thread-like nucleocapsid Mononegavirales Orthomyxoviridae Arenaviridae Bunyaviridae Coronaviridae Ophioviridae Roniviridae Globuloviridae Plasmaviridae Irregular or cone-shaped nucleocapsid Retroviridae Helical nucleocapsid, elongated virions Lipothrixviridae Filoviridae Membrane-only Pleolipoviruses Baculoviridae Nudivirus Nimaviridae