Baumgartel D M, Howell S H
Biochim Biophys Acta. 1976 Dec 1;454(2):349-61. doi: 10.1016/0005-2787(76)90237-9.
A model of polyribosome function based on tape theory has been applied to the analysis of intact polyribosomes from Chlamydomonas reinhardi. The distribution of nascent polypeptide chains found on polyribosomes does not conform to the expected pattern in which small polypeptides are synthesized on small polyribosomes and large polypeptides on correspondingly large polyribosomes. This discrepancy was revealed in the analysis of specific activity of polyribosomes (radioactivity in nascent chains per ribosome) versus polyribosome size at labeling saturation. It was found that the specific activity of small polyribosomes was higher than predicted and that of large polyribosomes was lower. This finding was validated by measuring the sizes of nascent chains from various polyribosome size classes by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis. The presence of large polypeptides on small polyribosomes could be partially accounted for by the synthesis of polypeptides on chloroplast (chloramphenicol-sensitive) polyribosomes. A maximum peptide interval time of 10 s was estimated from the labeling kinetics of the nascent chains of mid-sized (cytoplasmic) polyribosomes. This rate of translation is comparable to that reported in other eucaryotic cells.
基于磁带理论的多核糖体功能模型已应用于莱茵衣藻完整多核糖体的分析。在多核糖体上发现的新生多肽链的分布不符合预期模式,即小多肽在小多核糖体上合成,大多肽在相应的大多核糖体上合成。这种差异在标记饱和时多核糖体比活性(每个核糖体新生链中的放射性)与多核糖体大小的分析中得以揭示。发现小多核糖体的比活性高于预测值,而大多核糖体的比活性低于预测值。通过十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳测量不同多核糖体大小类别的新生链大小,验证了这一发现。小多核糖体上存在大多肽可部分归因于叶绿体(对氯霉素敏感)多核糖体上多肽的合成。从中等大小(细胞质)多核糖体新生链的标记动力学估计出最大肽间隔时间为10秒。这种翻译速率与其他真核细胞中报道的速率相当。