Kaufman R J
Howard Hughes Medical Institute, Department of Biological Chemistry, University of Michigan Medical Center, Ann Arbor 48105.
Curr Opin Biotechnol. 1994 Oct;5(5):550-7. doi: 10.1016/0958-1669(94)90073-6.
Protein synthesis is controlled at the level of translation initiation. Cells rapidly respond to environmental changes by disassembly of polysomes and recruitment of specific mRNAs from inactive ribonucleoprotein particles into polysomes active in translation. Recent insights have elucidated specific protein and RNA sequence interactions that are required to mobilize translation of selective mRNAs. The specificity of translational control provides a unique target to inhibit synthesis of specific polypeptides to control infectious disease as well as to control aberrant cell growth. In addition, greater understanding of the factors that limit protein synthesis is enabling the design of novel strategies to optimize protein expression and engineer host cells for enhanced growth and protein synthesis capacity.
蛋白质合成在翻译起始水平受到调控。细胞通过多聚核糖体的解体以及将特定mRNA从无活性的核糖核蛋白颗粒招募到活跃翻译的多聚核糖体中,快速响应环境变化。最近的研究揭示了动员选择性mRNA翻译所需的特定蛋白质和RNA序列相互作用。翻译控制的特异性为抑制特定多肽的合成以控制传染病以及控制异常细胞生长提供了独特的靶点。此外,对限制蛋白质合成因素的更深入了解有助于设计新策略来优化蛋白质表达,并改造宿主细胞以提高生长和蛋白质合成能力。