Three-dimensional structure of 22 uncultured ssRNA bacteriophages: Flexibility of the coat protein fold and variations in particle shapes

Capsid structures reveal a remarkable structural diversity among small bacterial RNA viruses. The single-stranded RNA (ssRNA) bacteriophages are among the simplest known viruses with small genomes and exceptionally high mutation rates. The number of ssRNA phage isolates has remained very low, but re...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Science advances Ročník 6; číslo 36
Hlavní autoři: Rūmnieks, Jānis, Liekniņa, Ilva, Kalniņš, Gints, Šišovs, Mihails, Akopjana, Ināra, Bogans, Jānis, Tārs, Kaspars
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States American Association for the Advancement of Science 01.09.2020
Témata:
SciAdv r-articles
Structural Biology
ISSN:2375-2548, 2375-2548
On-line přístup:Získat plný text
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!
Popis
Shrnutí:Capsid structures reveal a remarkable structural diversity among small bacterial RNA viruses. The single-stranded RNA (ssRNA) bacteriophages are among the simplest known viruses with small genomes and exceptionally high mutation rates. The number of ssRNA phage isolates has remained very low, but recent metagenomic studies have uncovered an immense variety of distinct uncultured ssRNA phages. The coat proteins (CPs) in these genomes are particularly diverse, with notable variation in length and often no recognizable similarity to previously known viruses. We recombinantly expressed metagenome-derived ssRNA phage CPs to produce virus-like particles and determined the three-dimensional structure of 22 previously uncharacterized ssRNA phage capsids covering nine distinct CP types. The structures revealed substantial deviations from the previously known ssRNA phage CP fold, uncovered an unusual prolate particle shape, and revealed a previously unseen dsRNA binding mode. These data expand our knowledge of the evolution of viral structural proteins and are of relevance for applications such as ssRNA phage–based vaccine design.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2375-2548
2375-2548
DOI:10.1126/sciadv.abc0023