文献类型: 外文期刊
作者: Yang, Mo 1 ; Li, Zehou 1 ; Chen, Jing 2 ; Li, Yang 2 ; Xu, Ran 3 ; Wang, Meihua 2 ; Xu, Ying 1 ; Chen, Rong 4 ; Ji, Weiwei 1 ; Li, Xiaoxia 1 ; Wei, Jiayu 1 ; Zhou, Zhengrong 1 ; Ren, Minjie 1 ; Ma, Ke 1 ; Guan, Jiayu 1 ; Mo, Guoxiang 1 ; Zhou, Peng 5 ; Shu, Bo 2 ; Guo, Jingjing 3 ; Yuan, Yuan 6 ; Shi, Zheng-Li 2 ; Zhang, Shuijun 1 ;
作者机构: 1.Nanjing Agr Univ, Coll Life Sci, Nanjing, Peoples R China
2.Chinese Acad Sci, Wuhan Inst Virol, Key Lab Virol & Biosafety, Wuhan, Peoples R China
3.Macao Polytech Univ, Fac Appl Sci, Ctr Artificial Intelligence Driven Drug Discovery, Taipa, Macao, Peoples R China
4.Jiangsu Acad Agr Sci, Inst Vet Med, Key Lab Vet Biol Engn & Technol, Minist Agr, Nanjing, Peoples R China
5.Guangzhou Int Bio Isl, Guangzhou Lab, Guangzhou, Guangdong, Peoples R China
6.Anhui Univ, Sch Life Sci, Hefei, Anhui, Peoples R China
期刊名称:PLOS PATHOGENS ( 影响因子:4.9; 五年影响因子:5.4 )
ISSN: 1553-7366
年卷期: 2024 年 20 卷 11 期
页码:
收录情况: SCI
摘要: Middle East respiratory syndrome coronavirus (MERS-CoV) and the pangolin MERS-like coronavirus MjHKU4r-CoV-1 employ dipeptidyl peptidase 4 (DPP4) as an entry receptor. MjHKU4r-CoV-1 could infect transgenic mice expressing human DPP4. To understand the mechanism of MjHKU4r-CoV-1 entry into cells, we determined the crystal structures of the receptor binding domain (RBD) of MjHKU4r-CoV-1 spike protein bound to human DPP4 (hDPP4) and Malayan pangolin DPP4 (MjDPP4), respectively. The overall hDPP4-binding mode of MjHKU4r-CoV-1 RBD is similar to that of MERS-CoV RBD. MjHKU4r-CoV-1 RBD shows higher binding affinity to hDPP4 compared to the bat MERS-like coronavirus Ty-BatCoV-HKU4. Via swapping residues between MjHKU4r-CoV-1 RBD and Ty-BatCoV-HKU4 RBD, we identified critical determinants on MjHKU4r-CoV-1 that are responsible for virus usage of hDPP4. Our study suggests that MjHKU4r-CoV-1 is more adapted to the human receptor compared to the bat HKU4 coronavirus and highlights the potential of virus emergence into the human population.
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