5CPU

Crystal structure of murine polyomavirus PTA strain VP1

5CPU の概要

• エントリーDOI: 10.2210/pdb5cpu/pdb
• 関連するPDBエントリー: 1VPN 1VPS
• 分子名称: VP1, GLYCEROL (3 entities in total)
• 機能のキーワード: murine polyomavirus, viral protein, carbohydrate complex, virus-host interaction
• 由来する生物種: Murine polyomavirus
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 158798.27

構造登録者

Liaci, A.M.,Buch, M.H.C.,Neu, U.,Stehle, T. (登録日: 2015-07-21, 公開日: 2015-10-28, 最終更新日: 2024-01-10)

主引用文献

Buch, M.H.,Liaci, A.M.,O'Hara, S.D.,Garcea, R.L.,Neu, U.,Stehle, T.
Structural and Functional Analysis of Murine Polyomavirus Capsid Proteins Establish the Determinants of Ligand Recognition and Pathogenicity.
Plos Pathog., 11:e1005104-e1005104, 2015

PubMed Abstract: Murine polyomavirus (MuPyV) causes tumors of various origins in newborn mice and hamsters. Infection is initiated by attachment of the virus to ganglioside receptors at the cell surface. Single amino acid exchanges in the receptor-binding pocket of the major capsid protein VP1 are known to drastically alter tumorigenicity and spread in closely related MuPyV strains. The virus represents a rare example of differential receptor recognition directly influencing viral pathogenicity, although the factors underlying these differences remain unclear. We performed structural and functional analyses of three MuPyV strains with strikingly different pathogenicities: the low-tumorigenicity strain RA, the high-pathogenicity strain PTA, and the rapidly growing, lethal laboratory isolate strain LID. Using ganglioside deficient mouse embryo fibroblasts, we show that addition of specific gangliosides restores infectability for all strains, and we uncover a complex relationship between virus attachment and infection. We identify a new infectious ganglioside receptor that carries an additional linear [α-2,8]-linked sialic acid. Crystal structures of all three strains complexed with representative oligosaccharides from the three main pathways of ganglioside biosynthesis provide the molecular basis of receptor recognition. All strains bind to a range of sialylated glycans featuring the central [α-2,3]-linked sialic acid present in the established receptors GD1a and GT1b, but the presence of additional sialic acids modulates binding. An extra [α-2,8]-linked sialic acid engages a protein pocket that is conserved among the three strains, while another, [α-2,6]-linked branching sialic acid lies near the strain-defining amino acids but can be accommodated by all strains. By comparing electron density of the oligosaccharides within the binding pockets at various concentrations, we show that the [α-2,8]-linked sialic acid increases the strength of binding. Moreover, the amino acid exchanges have subtle effects on their affinity for the validated receptor GD1a. Our results indicate that both receptor specificity and affinity influence MuPyV pathogenesis.

PubMed: 26474293
DOI: 10.1371/journal.ppat.1005104

実験手法

X-RAY DIFFRACTION (1.64 Å)