生物发生
蛋白质稳态
生物
伴侣(临床)
核糖体
细胞生物学
蛋白质生物合成
蛋白质折叠
翻译(生物学)
信使核糖核酸
生物化学
核糖核酸
基因
医学
病理
作者
Fabián Morales-Polanco,Jae Ho Lee,Natália M. Barbosa,Judith Frydman
标识
DOI:10.1146/annurev-biodatasci-121721-095858
摘要
The formation of protein complexes is crucial to most biological functions. The cellular mechanisms governing protein complex biogenesis are not yet well understood, but some principles of cotranslational and posttranslational assembly are beginning to emerge. In bacteria, this process is favored by operons encoding subunits of protein complexes. Eukaryotic cells do not have polycistronic mRNAs, raising the question of how they orchestrate the encounter of unassembled subunits. Here we review the constraints and mechanisms governing eukaryotic co- and posttranslational protein folding and assembly, including the influence of elongation rate on nascent chain targeting, folding, and chaperone interactions. Recent evidence shows that mRNAs encoding subunits of oligomeric assemblies can undergo localized translation and form cytoplasmic condensates that might facilitate the assembly of protein complexes. Understanding the interplay between localized mRNA translation and cotranslational proteostasis will be critical to defining protein complex assembly in vivo.
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