首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma
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Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma

机译:蛋白质跨膜转移。 I.蛋白水解处理和未处理的新生免疫球蛋白轻链在鼠骨髓瘤的膜结合核糖体上的存在

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摘要

Fractionation of MOPC 41 DL-1 tumors revealed that the mRNA for the light chain of immunoglobulin is localized exclusively in membrane- bound ribosomes. It was shown that the translation product of isolated light chain mRNA in a heterologous protein-synthesizing system in vitro is larger than the authentic secreted light chain; this confirms similar results from several laboratories. The synthesis in vitro of a precursor protein of the light chain is not an artifact of translation in a heterologous system, because it was shown that detached polysomes, isolated from detergent-treated rough microsomes, not only contain nascent light chains which have already been proteolytically processed in vivo but also contain unprocessed nascent light chains. In vitro completion of these nascent light chains thus resulted in the synthesis of some chains having the same mol wt as the authentic secreted light chains, because of completion of in vivo proteolytically processed chains and of other chains which, due to the completion of unprocessed chains, have the same mol wt as the precursor of the light chain. In contrast, completion of the nascent light chains contained in rough microsomes resulted in the synthesis of only processed light chains. Taken together, these results indicate that the processing activity is present in isolated rough microsomes, that it is localized in the membrane moiety of rough microsomes, and, therefore, that it was most likely solubilized during detergent treatment used for the isolation of detached polysomes. Furthermore, these results established that processing in vivo takes place before completion of the nascent chain. The data also indicate that in vitro processing of nascent chains by rough microsomes is dependent on ribosome binding to the membrane. If the latter process is interfered with by aurintricarboxylic acid, rough microsomes also synthesize some unprocessed chains. The data presented in this paper have been interpreted in the light of a recently proposed hypothesis. This hypothesis, referred to as the signal hypothesis, is described in greater detail in the Discussion section.
机译:MOPC 41 DL-1肿瘤的分级显示,免疫球蛋白轻链的mRNA仅位于膜结合核糖体中。结果表明,在异源蛋白合成系统中,分离出的轻链mRNA的翻译产物比真实分泌的轻链要大。这证实了几个实验室的类似结果。轻链前体蛋白的体外合成不是异源系统中的翻译产物,因为已表明,从去污剂处理过的粗微粒体中分离出来的分离的多核糖体不仅包含已经被蛋白水解的新生轻链。在体内进行加工,但还含有未加工的新生轻链。由于体内蛋白水解加工的链和由于未加工链的完成而引起的其他链的完成,这些新生轻链的体外完成因此导致合成了一些具有与真实分泌的轻链相同摩尔重量的链。具有与轻链前体相同的mol wt。相反,粗微粒体中新生的轻链的完成导致仅加工的轻链的合成。综上所述,这些结果表明加工活性存在于分离的粗糙微粒体中,其位于粗糙微粒体的膜部分中,因此,在用于分离游离多核糖体的去污剂处理过程中最有可能被溶解。此外,这些结果证实了体内加工发生在新生链完成之前。数据还表明粗糙的微粒体在体外加工新生链取决于核糖体与膜的结合。如果后一过程受到金三羧酸的干扰,则粗糙的微粒体还会合成一些未加工的链。本文中提出的数据已根据最近提出的假设进行了解释。在讨论部分中将更详细地描述这个假设,即信号假设。

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