牛腺病毒3次要蛋白和核心蛋白的结构见解:桥接衣壳和基因组核心。

IF 4.5 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Hao Xiao , Hao Pang , Junquan Zhou , Hao Feng , Jingdong Song , Lingpeng Cheng , Li Wang , Hongrong Liu
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引用次数: 0

摘要

腺病毒是与人类和动物健康广泛相关的双链DNA病毒,作为治疗载体具有相当大的潜力。尽管进行了广泛的研究,但对腺病毒核心蛋白和次要衣壳蛋白的结构细节仍然知之甚少。本研究利用低温电子显微镜分析了乳突腺病毒属成员牛腺病毒3型(badv3)的结构。我们的结构表明badv3与人类腺病毒具有显著的结构保守性。为次要蛋白VI和核心蛋白V和Mu的先前未表征的区域构建了原子模型。该研究揭示了核心蛋白如何在基因组和衣壳之间架起桥梁,强调了蛋白V在加强衣壳稳定性和促进基因组释放方面的多方面作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Structural Insights into Minor and Core Proteins of Bovine Adenovirus 3: Bridging Capsid and Genomic Core

Structural Insights into Minor and Core Proteins of Bovine Adenovirus 3: Bridging Capsid and Genomic Core
Adenoviruses are double-stranded DNA viruses with broad relevance to human and animal health and considerable potential as therapeutic vectors. Despite extensive studies, the structural details of core and minor capsid proteins in adenoviruses remain poorly understood. In this study, the architecture of bovine adenovirus type 3 (BAdV-3), a member of the Mastadenovirus genus, was solved by cryo-electron microscopy. Our structure shows that BAdV-3 shares significant structural conservation with human adenoviruses. Atomic models were constructed for a previously uncharacterized region of the minor protein VI and for the core proteins V and Mu. The study revealed how core proteins bridge the genome and capsid, underscore the multifaceted roles of protein V in strengthening capsid stability and facilitating genome release.
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来源期刊
Journal of Molecular Biology
Journal of Molecular Biology 生物-生化与分子生物学
CiteScore
11.30
自引率
1.80%
发文量
412
审稿时长
28 days
期刊介绍: Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions. Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.
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