6G01

Complex of neuraminidase from H1N1 influenza virus with tamiphosphor monomethyl ester

6G01 の概要

• エントリーDOI: 10.2210/pdb6g01/pdb
• 関連するPDBエントリー: 6G02
• 分子名称: Neuraminidase, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (9 entities in total)
• 機能のキーワード: neuraminidase, influenza, complex, inhibitor, viral protein
• 由来する生物種: Influenza A virus (A/Texas/17/2009(H1N1))
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 89086.82

構造登録者

Pachl, P.,Pokorna, J. (登録日: 2018-03-15, 公開日: 2019-01-23, 最終更新日: 2024-10-23)

主引用文献

Kozisek, M.,Navratil, V.,Rojikova, K.,Pokorna, J.,Berenguer Albinana, C.,Pachl, P.,Zemanova, J.,Machara, A.,Sacha, P.,Hudlicky, J.,Cisarova, I.,Rezacova, P.,Konvalinka, J.
DNA-linked inhibitor antibody assay (DIANA) as a new method for screening influenza neuraminidase inhibitors.
Biochem. J., 475:3847-3860, 2018

PubMed Abstract: Influenza neuraminidase is responsible for the escape of new viral particles from the infected cell surface. Several neuraminidase inhibitors are used clinically to treat patients or stockpiled for emergencies. However, the increasing development of viral resistance against approved inhibitors has underscored the need for the development of new antivirals effective against resistant influenza strains. A facile, sensitive, and inexpensive screening method would help achieve this goal. Recently, we described a multiwell plate-based DNA-linked inhibitor antibody assay (DIANA). This highly sensitive method can quantify femtomolar concentrations of enzymes. DIANA also has been applied to high-throughput enzyme inhibitor screening, allowing the evaluation of inhibition constants from a single inhibitor concentration. Here, we report the design, synthesis, and structural characterization of a tamiphosphor derivative linked to a reporter DNA oligonucleotide for the development of a DIANA-type assay to screen potential influenza neuraminidase inhibitors. The neuraminidase is first captured by an immobilized antibody, and the test compound competes for binding to the enzyme with the oligo-linked detection probe, which is then quantified by qPCR. We validated this novel assay by comparing it with the standard fluorometric assay and demonstrated its usefulness for sensitive neuraminidase detection as well as high-throughput screening of potential new neuraminidase inhibitors.

PubMed: 30404922
DOI: 10.1042/BCJ20180764

実験手法

X-RAY DIFFRACTION (1.61 Å)