在体上菌体L装饰蛋白的模板三元化
Brianna M Woodbury1, Rebecca L Newcomer1, Makayla N Leroux1
1Department of Molecular and Cell Biology, University of Connecticut, Storrs, Connecticut, USA.
Protein science : a publication of the Protein Society
|March 18, 2025
概括
体L装饰蛋白 (Dec) 形成了一个稳定的三元体,对于体相互作用至关重要. 体模板化在体内动态加快了Decrimer组件的组装,允许适应结合点.
科学领域:
- 结构生物学是结构生物学.
- 病毒学 病毒学
- 生物化学 生物化学
背景情况:
- 体L装饰蛋白 (Dec) 是一个134残留的同型三聚体.
- Dec稳定了菌体L囊体,具有不对称的三脚架状结构.
- OB-fold域与菌体病毒相互作用,而C-终端尖端稳定了三元体.
研究的目的:
- 调查Dec的C端尖端在囊相互作用中的作用.
- 确定 Dec Trimer 组件的机制和动力学.
- 探索病毒体对蛋白质寡合化的影响.
主要方法:
- 局部导向的突变发生,以产生DEC删除突变 (Dec1-98>).
- 酸性和pH控制的重新折叠实验,以研究trimer拆卸和重新组装.
- 对 Dec 突变体与菌体 P22 病毒体结合的分析.
主要成果:
- Dec1-98突变显示了OB折叠域的独立折叠,但缺乏稳定的囊结合.
- 全长的Dec在低pH (<2) 时分解成单体,带有未折叠的尖峰.
- 在pH 6下,Dec单体在体外重新组装成三元体是缓慢的 (几天).
- 在体内,Dec缩剂组件很可能是由菌体囊形成的模板.
结论:
- Dec的C端尖峰对于稳定的菌体囊相互作用至关重要.
- 病毒囊体模板化动力加快了体内 Dec Trimer 组装的速度.
- 这种模板机制使得Dec能够适应菌体上准对称的结合点.
相关概念视频
Lytic Cycle of Bacteriophages
70.1K
Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the...
70.1K
Lysogenic Cycle of Bacteriophages
61.6K
In contrast to the lytic cycle, phages infecting bacteria via the lysogenic cycle do not immediately kill their host cell. Instead, they combine their genome with the host genome, allowing the bacteria to replicate the phage DNA along with the bacterial genome. The incorporated copy of the phage genome is called the prophage. Some prophages can re-activate and enter the lytic cycle. This often occurs in response to a perturbation, such as DNA damage, but can also transpire in the absence of...
61.6K
Viral Structure
61.5K
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.
61.5K
Pinching-off of Coated Vesicles
3.0K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
3.0K
Protein Complex Assembly
10.5K
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...
10.5K


