| Literature DB >> 32004500 |
Fanli Yang1, Sheng Lin1, Fei Ye1, Jing Yang1, Jianxun Qi2, Zhujun Chen1, Xi Lin1, Jichao Wang1, Dan Yue1, Yanwei Cheng1, Zimin Chen1, Hua Chen1, Yu You1, Zhonglin Zhang1, Yu Yang1, Ming Yang1, Honglu Sun1, Yuhua Li3, Yu Cao4, Shengyong Yang1, Yuquan Wei1, George F Gao5, Guangwen Lu6.
Abstract
Rabies virus (RABV), the etiological agent for the lethal disease of rabies, is a deadly zoonotic pathogen. The RABV glycoprotein (RABV-G) is a key factor mediating virus entry and the major target of neutralizing antibodies. Here, we report the crystal structures of RABV-G solved in the free form at ∼pH-8.0 and in the complex form with a neutralizing antibody 523-11 at ∼pH-6.5, respectively. RABV-G has three domains, and the basic-to-acidic pH change results in large domain re-orientations and concomitant domain-linker re-constructions, switching it from a bent hairpin conformation into an extended conformation. During such low-pH-induced structural transitions, residues located in the domain-linker are found to play important roles in glycoprotein-mediated membrane fusion. Finally, the antibody interacts with RABV-G mainly through its heavy chain and binds to a bipartite conformational epitope in the viral protein for neutralization. These structures provide valuable information for vaccine and drug design.Entities:
Keywords: antibody-neutralization mechanism; crystal structure; glycoprotein; low-pH-induced structural transition; rabies virus; transition basis
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Year: 2020 PMID: 32004500 DOI: 10.1016/j.chom.2019.12.012
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023