The
polysome structure is essential for efficient protein synthesis in cells.
细胞内的多聚核糖体结构对于蛋白质合成至关重要。
During cell growth, the number of
polysomes increases to meet the demand for new proteins.
在细胞生长过程中,多聚核糖体的数量会增加以满足新蛋白质的需求。
Ribosomes can associate to form large
polysomes on mRNA molecules during translation.
翻译过程中,核糖体可以结合形成大的多聚核糖体在mRNA分子上。
The eukaryotic ribosome is involved in the formation of multiple
polysomes in the cytoplasm.
真核细胞中的核糖体参与细胞质中多聚核糖体的形成。
In a stress response, cells often halt
polysome assembly to conserve energy.
在应激反应中,细胞常常暂停多聚核糖体组装以节省能量。
The
polysome profiling technique helps researchers understand gene expression patterns.
多聚核糖体分析技术帮助研究人员理解基因表达模式。
The release of nascent peptides from
polysomes is facilitated by the action of chaperone proteins.
伴侣蛋白的作用有助于从多聚核糖体释放新生肽链。
The degradation of damaged or unnecessary
polysomes is a cellular quality control mechanism.
对受损或不必要的多聚核糖体的降解是细胞质量控制的一种机制。
The drug translation inhibitors target specific
polysomes to halt viral protein production.
翻译抑制剂针对特定的多聚核糖体,阻止病毒蛋白质的产生。
In eukaryotes,
polysomes are often found in rough endoplasmic reticulum (RER) for proper protein folding.
在真核细胞中,多聚核糖体通常位于糙面内质网上,以利于蛋白质正确折叠。
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