Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142, USA.
J Biol Chem. 2012 Oct 19;287(43):36528-35. doi: 10.1074/jbc.X112.420356. Epub 2012 Sep 17.
For the past fifty-five years, much of my research has focused on the function and biogenesis of red blood cells, including the cloning and study of many membrane proteins such as glucose and anion transporters and the erythropoietin receptor. We have also elucidated the mechanisms of membrane insertion, folding, and maturation of many plasma membrane and secreted proteins. Despite all of this work and more, I remain extremely proud of our very early work on the regulation of mRNA translation: work on bacteriophage f2 RNA in the 1960s and on translation of α- and β-globin mRNAs in the early 1970s. Using techniques hopelessly antiquated by today's standards, we correctly elucidated many important aspects of translational control, and I thought readers would be interested in learning how we did these experiments.
在过去的五十年里,我的大部分研究都集中在红细胞的功能和生物发生上,包括克隆和研究许多膜蛋白,如葡萄糖和阴离子转运体以及促红细胞生成素受体。我们还阐明了许多质膜和分泌蛋白的膜插入、折叠和成熟的机制。尽管做了所有这些工作,我仍然对我们早期在 mRNA 翻译调控方面的工作感到非常自豪:20 世纪 60 年代研究噬菌体 f2 RNA,20 世纪 70 年代早期研究α和β珠蛋白 mRNA 的翻译。使用的技术与今天的标准相比已经过时,我们正确地阐明了翻译控制的许多重要方面,我认为读者会有兴趣了解我们是如何进行这些实验的。