在膜化原细胞中,适应性ATP诱导的分子凝聚
Vincent Mukwaya1, Xiaolei Yu1, Shuo Yang1
1State Key Laboratory of Metal Matrix Composites, School of Materials Science and Engineering, Institute of Composite Materials, Shanghai Jiao Tong University, Shanghai 200240, People's Republic of China.
概括
研究人员创建了膜化原细胞,通过使用ATP控制分子凝结. 这种可控制的拥挤影响原细胞功能,酶活性和反应,在微反应器和药物输送中提供应用.
科学领域:
- 生物模拟化学是生物模拟化学.
- 原细胞的发展.
- 阶段分离的动态阶段分离的动态.
背景情况:
- 液-液相分离 (LLPS) 对细胞组织至关重要,但在原细胞模型中难以控制.
- 细胞内ATP水平影响蛋白质相互作用和细胞拥挤,影响凝结物的形成和溶解.
研究的目的:
- 使用非惰性 crowders 开发一个具有可控制分子凝聚的原细胞模型.
- 研究ATP诱导的拥挤对原细胞功能,酶活性和生物化学反应的影响.
主要方法:
- 使用微模板引导组装制造膜化原细胞 (多糖体).
- 通过ATP吸收诱导内源的LLPS和液体凝状相分离.
- 在拥挤的原细胞中评估酶活性和DNA链位移反应.
主要成果:
- 吸收ATP使可调节的细胞内LLPS和液体-凝类相分离成为可能.
- 在拥挤的原细胞中,酶活性增强,但在高凝结水平下降.
- 增加的分子拥挤抑制了细胞内DNA链位移反应.
结论:
- 建立了一种用于构建具有可控制分子拥挤和功能的膜化原细胞的新方法.
- 这些发现表明,在微反应器技术,传感和治疗输送系统方面有潜在的应用.
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