8VOM

Double alanine Apex domain mutant of bacteriophage P2 central spike protein, membrane-piercing module

これはPDB形式変換不可エントリーです。

8VOM の概要

• エントリーDOI: 10.2210/pdb8vom/pdb
• 分子名称: Spike protein, PHOSPHATIDYLETHANOLAMINE (3 entities in total)
• 機能のキーワード: membrane-piercing, phage, baseplate, trimer, viral protein
• 由来する生物種: Bacteriophage P2
• タンパク質・核酸の鎖数: 6
• 化学式量合計: 72725.69

構造登録者

Leiman, P.G.,Miller, J.M. (登録日: 2024-01-15, 公開日: 2024-08-07)

主引用文献

Miller, J.M.,Knyazhanskaya, E.S.,Buth, S.A.,Prokhorov, N.S.,Leiman, P.G.
Function of the bacteriophage P2 baseplate central spike Apex domain in the infection process.
bioRxiv, 2023

PubMed Abstract: The contractile tail of bacteriophage P2 functions to drive the tail tube across the outer membrane of its host bacterium, a prerequisite event for subsequent translocation of phage genomic DNA into the host cell. The tube is equipped with a spike-shaped protein (product of P2 gene , gpV or Spike) that contains a membrane-attacking Apex domain carrying a centrally positioned Fe ion. The ion is enclosed in a histidine cage that is formed by three symmetry-related copies of a conserved HxH (histidine, any residue, histidine) sequence motif. Here, we used solution biophysics and X-ray crystallography to characterize the structure and properties of Spike mutants in which the Apex domain was either deleted or its histidine cage was either destroyed or replaced with a hydrophobic core. We found that the Apex domain is not required for the folding of full-length gpV or its middle intertwined β-helical domain. Furthermore, despite its high conservation, the Apex domain is dispensable for infection in laboratory conditions. Collectively, our results show that the diameter of the Spike but not the nature of its Apex domain determines the efficiency of infection, which further strengthens the earlier hypothesis of a drill bit-like function of the Spike in host envelope disruption.

PubMed: 36865152
DOI: 10.1101/2023.02.25.529910

実験手法

X-RAY DIFFRACTION (1.25 Å)