低温电子显微
乙型肝炎病毒
协议(科学)
免疫原性
样板房
分辨率(逻辑)
计算机科学
工作流程
物理
病毒学
统计物理学
人工智能
生物
病毒
抗原
医学
粒子物理学
数据库
病理
替代医学
核磁共振
遗传学
作者
Nadia M. DiNunno,Emily N Bianchini,Haitao Liu,Joseph Che‐Yen Wang
出处
期刊:Bio-protocol
[American Academy of Arts and Sciences]
日期:2023-01-01
卷期号:13 (14): e4751-e4751
被引量:2
标识
DOI:10.21769/bioprotoc.4751
摘要
Hepatitis B virus (HBV) infection is a global public health concern. During chronic infection, the HBV small-surface antigen is expressed in large excess as non-infectious spherical subviral particles (SVPs), which possess strong immunogenicity. To date, attempts at understanding the structure of HBV spherical SVP have been restricted to 12-30 Å with contradictory conclusions regarding its architecture. We have used cryo-electron microscopy (cryo-EM) and 3D image reconstruction to solve the HBV spherical SVP to 6.3 Å. Here, we present an extended protocol on combining AlphaFold2 prediction with a moderate-resolution cryo-EM density map to build a reliable 3D model. This protocol utilizes multiple software packages that are routinely used in the cryo-EM community. The workflow includes 3D model prediction, model evaluation, rigid-body fitting, flexible fitting, real-space refinement, model validation, and model adjustment. Finally, the described protocol can also be applied to high-resolution cryo-EM datasets (2-4 Å).
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