类似病毒的囊体中的点突变驱动对称性减少,形成四面体子
Taylor N Szyszka1,2, Michael P Andreas3, Felicia Lie1
1School of Chemistry, The University of Sydney, Camperdown, NSW 2006, Australia.
bioRxiv : the preprint server for biology
|February 19, 2024
概括
最小的蛋白质突变可以改变病毒囊对称性. 一种细菌囊突变形成四面体结构,揭示了体组装的可塑性和超越二面体对称性的新型几何形状.
科学领域:
- 结构生物学是结构生物学.
- 生物化学 生物化学
- 病毒学 病毒学
背景情况:
- 蛋白质体对病毒结构和功能至关重要,通常表现出二面体对称,以最大限度地提高内部体积.
- 在病毒衍生的体中这种无处不在的二元对称性是结构生物学中长期存在的原则.
研究的目的:
- 研究点突变对病毒类蛋白质体的自我组装和对称性的影响.
- 探索产生超出典型的二面体形状的新型体几何形状的潜力.
主要方法:
- 质光学和本源电荷检测质谱学被用来分析体组件.
- 使用冷电子显微镜 (cryo-EM) 来确定产生的体的高分辨率结构.
主要成果:
- *Myxococcus xanthus*囊中的一个三重定点突变体形成了较小的二态组合.
- 冷电磁探测揭示了已知的60-mer双面体组件和一个新的36-mer四面体组件,具有重新排列的质子体相互作用.
- 通过各种突变可以实现四面体组件的形成,包括单一的histidine点突变.
结论:
- 这项研究报告了细菌囊,HK97类囊和蛋白质数据库中的病毒衍生囊中四面体几何学的第一个实例.
- 最小的遗传变化可以导致状体结构和对称性的显著变化,挑战已有的模型.
- 透露了通过向蛋白质序列修改来设计新型囊架构的潜力.
相关概念视频
Viral Structure
62.2K
Viruses are extraordinarily diverse in shape and size, but they all have several structural features in common. All viruses have a core that contains a DNA- or RNA-based genome. The core is surrounded by a protective coat of proteins called the capsid. The capsid is composed of subunits called capsomeres. The capsid and genome-containing core are together known as the nucleocapsid.
62.2K
Protein Complex Assembly
10.6K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types. Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Many viruses self-assemble into a fully functional unit using the infected host cell to...
10.6K
Amyloid Fibrils
9.5K
Amyloid fibrils are aggregates of misfolded proteins. Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils.
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
Amyloid deposits were observed as early as 1639 in the liver and the spleen. In 1854, Rudolph Virchow performed iodine staining,...
9.5K
Viral Recombination
23.4K
Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
23.4K
Intracellular Movement of Viruses and Bacteria
2.8K
Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a...
2.8K
Viral Mutations
32.3K
A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
32.3K


