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在噬菌体Ms2 RNA的核糖体结合中,干扰因子α取代核糖体蛋白S1。

Replacement of ribosomal protein S1 by interference factor ialpha in ribosomal binding of phage Ms2 RNA.

作者信息

Hermoso J M, Szer W

出版信息

Proc Natl Acad Sci U S A. 1974 Dec;71(12):4708-12. doi: 10.1073/pnas.71.12.4708.

DOI:10.1073/pnas.71.12.4708
PMID:4612526
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC433965/
Abstract

The MS2 RNA binding capacity of 30S ribosomal subunits, which is lost when protein S1 is removed, can be restored following incubation with interference factor ialpha and repelleting. Polyacrylamide-agarose gel electrophoresis shows that, under these conditions, a faster moving, non-RNA binding 30S species, which contains no S1, is converted to a slower moving RNA-binding one, having the same mobility as the 30S species that contains protein S1. Factor ialpha binds to single-stranded RNAs in a pattern that closely resembles the RNA binding pattern of initiation factor IF-3.

摘要

30S核糖体亚基的MS2 RNA结合能力在去除蛋白质S1时丧失,在与干扰因子α孵育并重新沉淀后可恢复。聚丙烯酰胺-琼脂糖凝胶电泳显示,在这些条件下,一种不含S1、迁移速度较快的非RNA结合30S物种转变为迁移速度较慢的RNA结合物种,其迁移率与含有蛋白质S1的30S物种相同。因子α以一种与起始因子IF-3的RNA结合模式非常相似的方式与单链RNA结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/68bbc5124c66/pnas00075-0072-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/5ac38f76a538/pnas00075-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/d7ba5073f6c4/pnas00075-0072-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/68bbc5124c66/pnas00075-0072-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/5ac38f76a538/pnas00075-0072-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/d7ba5073f6c4/pnas00075-0072-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65dc/433965/68bbc5124c66/pnas00075-0072-c.jpg

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本文引用的文献

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The conformational properties of ribosomal protein S1.核糖体蛋白S1的构象特性。
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