Suppr超能文献

分泌性和非分泌性组织的膜结合核糖体和游离核糖体的蛋白质合成。

Protein synthesis by membrane-bound and free ribosomes of secretory and non-secretory tissues.

作者信息

Andrews T M, Tata J R

出版信息

Biochem J. 1971 Feb;121(4):683-94. doi: 10.1042/bj1210683.

Abstract
  1. Methods for the separation of membrane-bound and free ribosomes from rat brain (cortex) and skeletal muscle were described and the preparations characterized by chemical analysis and electron microscopy. The attachment of ribosomes to membranes is not an artifact of the separation procedure. 2. The rate of incorporation of l-[(14)C]leucine into protein in vitro by the membrane-bound and free ribosomes from these two predominantly non-protein-secreting tissues is compared with that by similar preparations from rat liver. With all three tissues the initial rate was higher for the membrane-bound preparations. 3. By using the technique of discharging nascent polypeptide chains by incubation with puromycin followed by treatment with sodium deoxycholate (Redman & Sabatini, 1966), a major difference was observed for the vectorial discharge of nascent protein synthesized both in vivo and in vitro on membrane-bound ribosomes from liver, on the one hand, and brain and muscle, on the other. Whereas a large part of nascent protein synthesized on membrane-bound liver ribosomes was discharged into the membranous vesicles (presumably destined for export from the cell), almost all nascent protein from membrane-bound ribosomes from brain and muscle was released directly into the supernatant. Incorporation of [(3)H]puromycin into peptidyl-[(3)H]puromycin confirmed these findings. There was thus no difference between membrane-bound and free ribosomes from brain on the one hand, and from free polyribosomes from liver on the other, as far as the vectorial release of newly synthesized protein was concerned. 4. Incubation with puromycin also showed that the nascent chains, pre-formed in vivo and in vitro, are not involved in the attachment of ribosomes to membranes of the endoplasmic reticulum. 5. The differences in vectorial discharge from membrane-bound ribosomes from liver as compared with brain and muscle are not due to the different types of messenger RNA in the different tissues. Polyphenylalanine synthesized on incubation with polyuridylic acid was handled in the same way as polypeptides synthesized with endogenous messenger. 6. It is concluded that there is a major difference in the attachment of ribosomes to the membranes of the endoplasmic reticulum of secretory and non-secretory tissues, which results in a tissue-specific difference in the vectorial discharge of nascent proteins.
摘要
  1. 描述了从大鼠脑(皮层)和骨骼肌中分离膜结合核糖体和游离核糖体的方法,并通过化学分析和电子显微镜对制备物进行了表征。核糖体与膜的附着并非分离过程中的人为产物。2. 将来自这两种主要非蛋白质分泌组织的膜结合核糖体和游离核糖体在体外将 l-[(14)C]亮氨酸掺入蛋白质的速率与来自大鼠肝脏的类似制备物的速率进行了比较。对于所有三种组织,膜结合制备物的初始掺入速率更高。3. 通过使用与嘌呤霉素孵育然后用脱氧胆酸钠处理来释放新生多肽链的技术(Redman & Sabatini,1966),观察到一个主要差异,即一方面,在肝脏的膜结合核糖体上体内和体外合成的新生蛋白质的定向释放,与另一方面脑和肌肉的情况不同。在肝脏膜结合核糖体上合成的大部分新生蛋白质被释放到膜泡中(可能注定要从细胞中输出),而来自脑和肌肉的膜结合核糖体的几乎所有新生蛋白质都直接释放到上清液中。[(3)H]嘌呤霉素掺入肽基-[(3)H]嘌呤霉素证实了这些发现。因此,就新合成蛋白质的定向释放而言,脑的膜结合核糖体和游离核糖体与肝脏的游离多核糖体之间没有差异。4. 与嘌呤霉素孵育还表明,在体内和体外预先形成的新生链不参与核糖体与内质网膜的附着。5. 与脑和肌肉相比,肝脏膜结合核糖体定向释放的差异不是由于不同组织中不同类型的信使 RNA 所致。与聚尿苷酸一起孵育合成的聚苯丙氨酸的处理方式与用内源性信使合成的多肽相同。6. 得出的结论是,分泌组织和非分泌组织的核糖体与内质网膜的附着存在主要差异,这导致新生蛋白质的定向释放存在组织特异性差异。

相似文献

3
Difference in vectorial release of nascent protein from membrane-bound ribosomes of secretory and non-secretory tissues.
Biochem Biophys Res Commun. 1968 Sep 30;32(6):1050-6. doi: 10.1016/0006-291x(68)90136-8.
4
Production of membrane whorls in rat liver by some inhibitors of protein synthesis.
J Cell Biol. 1974 Jul;62(1):20-31. doi: 10.1083/jcb.62.1.20.
5
The in vitro reconstitution of a functional rough membrane active in protein synthesis.
Mol Biol Rep. 1975 Mar;2(1):73-9. doi: 10.1007/BF00357300.
10
In vitro synthesis of different categories of specific protein by membrane-bound and free ribosomes.
Proc Natl Acad Sci U S A. 1969 Aug;63(4):1370-6. doi: 10.1073/pnas.63.4.1370.

引用本文的文献

2
SCENITH: A Flow Cytometry-Based Method to Functionally Profile Energy Metabolism with Single-Cell Resolution.
Cell Metab. 2020 Dec 1;32(6):1063-1075.e7. doi: 10.1016/j.cmet.2020.11.007.
3
Properties of Cavities in Biological Structures-A Survey of the Protein Data Bank.
Front Mol Biosci. 2020 Nov 6;7:591381. doi: 10.3389/fmolb.2020.591381. eCollection 2020.
4
TePhe, a tellurium-containing phenylalanine mimic, allows monitoring of protein synthesis in vivo with mass cytometry.
Proc Natl Acad Sci U S A. 2019 Apr 23;116(17):8155-8160. doi: 10.1073/pnas.1821151116. Epub 2019 Apr 10.
5
The Sec System: Protein Export in .
EcoSal Plus. 2017 Nov;7(2). doi: 10.1128/ecosalplus.ESP-0002-2017.
7
Ribosomal proteins and human diseases: pathogenesis, molecular mechanisms, and therapeutic implications.
Med Res Rev. 2015 Mar;35(2):225-85. doi: 10.1002/med.21327. Epub 2014 Aug 28.
9
Imaging protein synthesis in cells and tissues with an alkyne analog of puromycin.
Proc Natl Acad Sci U S A. 2012 Jan 10;109(2):413-8. doi: 10.1073/pnas.1111561108. Epub 2011 Dec 12.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.
J Biol Chem. 1951 Nov;193(1):265-75.
4
The precision of ultraviolet absorption measurements in the Schmidt-Thannhauser procedure for nucleic acid estimation.
Biochim Biophys Acta. 1962 May 14;55:571-83. doi: 10.1016/0006-3002(62)90836-3.
8
Membrane-bound ribonucleic acid in mammalian erythroid cells.
Biochemistry. 1967 Sep;6(9):2840-7. doi: 10.1021/bi00861a026.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验