在AP分析中,AP分析解决了同翻译折叠路径和伴侣相互作用in vivo
Xiuqi Chen1,2,3, Christian M Kaiser2,4
1CMDB Graduate Program, Johns Hopkins University, Baltimore, MD, United States.
bioRxiv : the preprint server for biology
|September 11, 2023
概括
我们开发了Arrest Peptide分析 (AP分析) 来测量活细胞合成过程中的蛋白质折叠. 这种方法揭示了蛋白质结构和陪伴物如何影响共同翻译折叠路径.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
- 细胞生物学 细胞生物学
背景情况:
- 蛋白质折叠对细胞功能至关重要,但共同翻译折叠仍然不太了解.
- 现有的方法很难准确地测量复杂的细胞环境中的折叠.
研究的目的:
- 开发一种高通量方法来量化活细胞中的同翻译折叠.
- 为了研究蛋白质拓和分子伴侣如何影响折叠路径.
主要方法:
- 开发了一种新的高吞吐量技术 - - 逮捕形状 (AP 形状) 分析.
- 应用AP剖析来研究GTPase域和伴随性切除的影响.
主要成果:
- 划出了GTPase域的共同翻译折叠路径,突出了拓学的作用.
- 在陪伴者基因切除后观察到局部折叠变化,这表明功能冗余机制.
结论:
- 在研究新生的蛋白质折叠过程中,AP分析提供了前所未有的分辨率和吞吐量.
- 这项工作提供了关于细胞折叠机制和伴侣相互作用的见解.
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