4QZV

Bat-derived coronavirus HKU4 uses MERS-CoV receptor human CD26 for cell entry

4QZV の概要

• エントリーDOI: 10.2210/pdb4qzv/pdb
• 関連するPDBエントリー: 4KR0
• 分子名称: Dipeptidyl peptidase 4, Spike protein S1, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (6 entities in total)
• 機能のキーワード: 8-bladed beta-propeller domain, alpha/beta hydrolase domain, blades iv and v, cd26 beta-propeller, hydrolase-viral protein complex, hydrolase/viral protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 229455.56

構造登録者

Gao, F.G.,Wang, Q.H.,Qi, J.X.,Lu, G.W. (登録日: 2014-07-29, 公開日: 2014-10-29, 最終更新日: 2024-11-20)

主引用文献

Wang, Q.H.,Qi, J.X.,Yuan, Y.,Xuan, Y.,Han, P.,Wan, Y.,Ji, W.,Li, Y.,Wu, Y.,Wang, J.,Iwamoto, A.,Woo, P.C.,Yuen, K.Y.,Yan, J.,Lu, G.W.,Gao, G.F.
Bat Origins of MERS-CoV Supported by Bat Coronavirus HKU4 Usage of Human Receptor CD26.
Cell Host Microbe, 16:328-337, 2014

PubMed Abstract: The recently reported Middle East respiratory syndrome coronavirus (MERS-CoV) is phylogenetically closely related to the bat coronaviruses (BatCoVs) HKU4 and HKU5. However, the evolutionary pathway of MERS-CoV is still unclear. A receptor binding domain (RBD) in the MERS-CoV envelope-embedded spike protein specifically engages human CD26 (hCD26) to initiate viral entry. The high sequence identity in the viral spike protein prompted us to investigate if HKU4 and HKU5 can recognize hCD26 for cell entry. We found that HKU4-RBD, but not HKU5-RBD, binds to hCD26, and pseudotyped viruses embedding HKU4 spike can infect cells via hCD26 recognition. The structure of the HKU4-RBD/hCD26 complex revealed a hCD26-binding mode similar overall to that observed for MERS-RBD. HKU4-RBD, however, is less adapted to hCD26 than MERS-RBD, explaining its lower affinity for receptor binding. Our findings support a bat origin for MERS-CoV and indicate the need for surveillance of HKU4-related viruses in bats.

PubMed: 25211075
DOI: 10.1016/j.chom.2014.08.009

実験手法

X-RAY DIFFRACTION (2.592 Å)