7CN2
Subparticle refinement of human papillomavirus type 16 pesudovirus in complex with H16.001 Fab
7CN2 の概要
| エントリーDOI | 10.2210/pdb7cn2/pdb |
| EMDBエントリー | 30414 |
| 分子名称 | The light chain variable region of H16.001 Fab fragment, The heavy chain variable region of H16.001 Fab fragment, Major capsid protein L1 (3 entities in total) |
| 機能のキーワード | virus, immune complex, immune system-viral protein complex, immune system/viral protein |
| 由来する生物種 | Human papillomavirus type 16 詳細 |
| タンパク質・核酸の鎖数 | 18 |
| 化学式量合計 | 486381.04 |
| 構造登録者 | |
| 主引用文献 | Huang, W.,He, M.,Ning, T.,Nie, J.,Zhang, F.,Zheng, Q.,Zhang, R.,Xu, Y.,Gu, Y.,Li, S.,Wang, Y. Structural characterization of a neutralizing mAb H16.001, a potent candidate for a common potency assay for various HPV16 VLPs. Npj Vaccines, 5:89-89, 2020 Cited by PubMed Abstract: With more human papillomavirus (HPV) virus-like particle (VLP) vaccines to hit the market in future, a monoclonal antibody (mAb) with preferably comparable reactivity against vaccines from different expression systems and bioprocesses is urgently needed for the potency characterization. Among all mAbs against HPV16 collected, rabbit mAb H16.001 is potently neutralizing with the highest affinity, recognizes an immune-dominant epitope, and can comparably react with HPV16 vaccines from various sources. Cryo-electron microscopic (cryo-EM) structure demonstrated that 360 H16.001 Fabs could bind to HPV16 capsid in preferable binding manner without steric hindrance between neighboring Fabs, potentially supporting its identification for VLP structural integrity and utility in monitoring VLP structural probity. This structural analysis indicated that mAb H16.001 afforded unbiased potency characterization for various HPV16 vaccines and was potential for use in vaccine regulation practice. This study also showed a model process for selecting suitable mAbs for potency assays of other vaccines. PubMed: 33042588DOI: 10.1038/s41541-020-00236-w 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (3.43 Å) |
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