Nomura M
Science. 1973 Mar 2;179(4076):864-73. doi: 10.1126/science.179.4076.864.
I have not mentioned the remarkable progress made mainly by Fellner and his co-workers (86) in the elucidation of the primary structure of rRNA's and by Wittmann and his co-workers (87) in determining the structure of several ribosomal proteins. Such knowledge of primary structures is certainly the basis of complete understanding of the structure of the ribosome. With the current progress in technology, complete elucidation of the primary structure of all the ribosomal components is probably a matter of time. As indicated in this article, a rough approximation of the three-dimensional structure of ribosomes is likely to emerge soon. Although not mentioned in this article, studies of ribosomes from higher organisms are also progressing. We must, therefore, consider what further studies should be conducted and what kinds of questions we would like to solve. Some groups of investigators aim to elucidate the complete three-dimensional structure of ribosomes and to find out how these complex cell organelles function; they hope to determine the conformational changes of many of the component molecules within the ribosome structure in response to external macromolecules and cofactors engaged in protein synthesis. Such knowledge will also be important in enabling us to understand the regulation of translation of genetic messages. Other groups of investigators aim to elucidate the complex series of events which originate in the transcription of the more than 60 genes and culminate in the formation of the specific structure of the organelle. Complete reproduction in vitro of all the assembly events that occur in vivo should not be difficult to achieve in principle. It should then become possible to study in vitro any factor regulating the biogenesis of the organelle. Although we do not know whether such studies would reveal any new fundamental principle that governs the complex circuits of interconnected macromolecular interactions, the achievement of such a complete in vitro system would represent a necessary step in the comprehensive understanding of biogenesis of organelles, and eventually, of the more complex behavior and genesis of cells (89).
我尚未提及费尔纳及其同事(86)在阐明核糖体RNA一级结构方面以及维特曼及其同事(87)在确定几种核糖体蛋白质结构方面所取得的显著进展。这种一级结构的知识无疑是全面理解核糖体结构的基础。随着当前技术的进步,完全阐明所有核糖体组分的一级结构可能只是时间问题。如本文所述,核糖体三维结构的大致轮廓可能很快就会显现。尽管本文未提及,但对高等生物核糖体的研究也在取得进展。因此,我们必须考虑应进行哪些进一步的研究以及我们希望解决哪些类型的问题。一些研究小组旨在阐明核糖体的完整三维结构,并弄清楚这些复杂的细胞器是如何发挥功能的;他们希望确定核糖体结构内许多组分分子在与参与蛋白质合成的外部大分子和辅助因子相互作用时的构象变化。这样的知识对于我们理解遗传信息的翻译调控也将非常重要。其他研究小组旨在阐明一系列复杂的事件,这些事件始于60多个基因的转录,最终导致细胞器特定结构的形成。原则上,在体外完全重现体内发生的所有组装事件应该不难实现。届时,就有可能在体外研究任何调节细胞器生物发生的因素。尽管我们不知道这样的研究是否会揭示任何支配相互连接的大分子相互作用复杂网络的新基本原理,但实现这样一个完整的体外系统将是全面理解细胞器生物发生以及最终理解细胞更复杂行为和起源的必要步骤(89)。