4Q4V

Crystal structure of Coxsackievirus A24v

4Q4V の概要

• エントリーDOI: 10.2210/pdb4q4v/pdb
• 関連するPDBエントリー: 4Q4W 4Q4X 4Q4Y
• 分子名称: Coxsackievirus capsid protein VP1, Coxsackievirus capsid protein VP2, Coxsackievirus capsid protein VP3, ... (4 entities in total)
• 機能のキーワード: coxsackievirus a24v, virus
• 由来する生物種: Coxsackievirus A24; 詳細
• 細胞内の位置: Host cytoplasm (By similarity). Host cytoplasmic vesicle membrane; Peripheral membrane protein; Cytoplasmic side (By similarity): V9VEF3 V9VEF3 V9VEF3 V9VEF3
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 98152.57

構造登録者

Zocher, G.,Stehle, T. (登録日: 2014-04-15, 公開日: 2014-11-05, 最終更新日: 2024-02-28)

主引用文献

Zocher, G.,Mistry, N.,Frank, M.,Hahnlein-Schick, I.,Ekstrom, J.O.,Arnberg, N.,Stehle, T.
A sialic Acid binding site in a human picornavirus.
Plos Pathog., 10:e1004401-e1004401, 2014

PubMed Abstract: The picornaviruses coxsackievirus A24 variant (CVA24v) and enterovirus 70 (EV70) cause continued outbreaks and pandemics of acute hemorrhagic conjunctivitis (AHC), a highly contagious eye disease against which neither vaccines nor antiviral drugs are currently available. Moreover, these viruses can cause symptoms in the cornea, upper respiratory tract, and neurological impairments such as acute flaccid paralysis. EV70 and CVA24v are both known to use 5-N-acetylneuraminic acid (Neu5Ac) for cell attachment, thus providing a putative link between the glycan receptor specificity and cell tropism and disease. We report the structures of an intact human picornavirus in complex with a range of glycans terminating in Neu5Ac. We determined the structure of the CVA24v to 1.40 Å resolution, screened different glycans bearing Neu5Ac for CVA24v binding, and structurally characterized interactions with candidate glycan receptors. Biochemical studies verified the relevance of the binding site and demonstrated a preference of CVA24v for α2,6-linked glycans. This preference can be rationalized by molecular dynamics simulations that show that α2,6-linked glycans can establish more contacts with the viral capsid. Our results form an excellent platform for the design of antiviral compounds to prevent AHC.

PubMed: 25329320
DOI: 10.1371/journal.ppat.1004401

実験手法

X-RAY DIFFRACTION (2.9 Å)