分子拥挤对形成多个G-四重复的端粒突起的可访问性的影响
Golam Mustafa1, Sajad Shiekh1, Janan Alfehaid1
1Department of Physics, Kent State University, Kent, Ohio 44242, United States.
Biomacromolecules
|June 13, 2025
概括
分子拥挤压缩着端粒突起,减少探头的可访问性. 这项研究揭示了细胞环境如何影响G-四重复 (GQ) 结构和端粒结构.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 细胞生物物理学 细胞生物物理学
背景情况:
- 分子拥挤是细胞环境的关键特征.
- 拥挤影响G-四重复 (GQ) 折叠,形状和稳定性.
- 拥挤对端粒悬浮架构和GQ可访问性的影响还未得到充分研究.
研究的目的:
- 研究分子拥挤如何影响含有多个GQs的端粒突起的架构和可访问性.
- 在不同拥挤条件下量化测试探头可访问端粒悬浮的减少.
主要方法:
- 使用单分子弗斯特共振能量转移 (smFRET) 和FRET-PAINT技术.
- 检查的端粒突起能够形成1-6个GQ.
- 在不同度的聚乙烯糖醇 (PEG) 分子 (PEG-200和PEG-6000) 存在时,对核酸 (PNA) 探针的可访问性进行评估.
主要成果:
- 增加的PEG度导致了端粒突起的逐渐紧缩和建筑凝结.
- 在30%的PEG度下,PEG-200的探头可达性降低了大约3倍,PEG-6000的可达性降低了8倍.
- 拥挤大大降低了对补充PNA探针的端粒悬浮的可访问性.
结论:
- 分子拥挤压缩着端粒突起,改变了它们的结构.
- 拥挤调节了G-四重复结构在端粒突起中的可访问性.
- 这些发现提供了关于细胞环境在调节端粒结构和功能的作用的见解.
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