9E80

Canine parvovirus subtype 2a empty capsid in complex with Fab fragments of Mab 2C5

これはPDB形式変換不可エントリーです。

9E80 の概要

• エントリーDOI: 10.2210/pdb9e80/pdb
• EMDBエントリー: 47697
• 分子名称: Capsid protein 2 (1 entity in total)
• 機能のキーワード: virus, antibody, complex
• 由来する生物種: Canine parvovirus 2a
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 64745.56

構造登録者

Lee, H.,Hafenstein, S. (登録日: 2024-11-04, 公開日: 2025-01-29, 最終更新日: 2025-05-21)

主引用文献

Adu, O.F.,Lee, H.,Fruh, S.P.,Schoenle, M.V.,Weichert, W.S.,Flyak, A.I.,Hafenstein, S.L.,Parrish, C.R.
Structures and functions of the limited natural polyclonal antibody response to parvovirus infection.
Proc.Natl.Acad.Sci.USA, 122:e2423460122-e2423460122, 2025

PubMed Abstract: Host antibody responses are key components in the protection of animals against pathogens, yet the defining properties of viral antigens and induction of B cell responses that result in varied protection are still poorly understood. Parvoviruses are simple molecular structures that display 60 repeated motifs on their capsid surface, and rapidly induce strong antibody responses that protect animals from infection. We recently showed that following canine parvovirus infection of its natural host, the polyclonal response in the sera contained only two or three dominant antibodies that bound two epitopes on the capsid. Here, we characterize key antibodies present in that immune response, identifying their sequences, defining their binding properties on the capsid by cryoelectron microscopic (cryoEM) analysis, and testing their effects on viral infectivity. Two antibodies sharing the same heavy chain bound to the side of the capsid threefold spike (B-site), while another distinct antibody bound close to the threefold axis (A-site). The epitopes of these antibodies overlapped the binding site of the host receptor, the transferrin receptor type-1, but to varying degrees. The antibodies varied widely in their neutralization efficiencies as either immunoglobulins (IgGs) or monomeric antigen-binding fragments (Fabs), which was consistent with their ability to compete for the receptor. The monoclonal antibodies characterized here matched the structures from the cryoEM analysis of polyclonal sera, including those present in a different dog than the monoclonal source. This shows that after infection, a focused response to the viral antigen is produced that protects against infection.

PubMed: 39951487
DOI: 10.1073/pnas.2423460122

実験手法

ELECTRON MICROSCOPY (1.81 Å)