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核糖体蛋白S4和S8在16S RNA上结合位点的电子显微镜测定

Electron microscopic determination of the binding sites of ribosomal proteins S4 and S8 on 16S RNA.

作者信息

Cole M D, Beer M, Koller T, Strycharz W A, Nomura M

出版信息

Proc Natl Acad Sci U S A. 1978 Jan;75(1):270-4. doi: 10.1073/pnas.75.1.270.

Abstract

Specific complexes.early in the assembly of Escherichia coli ribosomes were examined in the electron microscope. Complexes between ribosomal protein S4 or S8 and 16S RNA were fixed gently with formaldehyde and then denatured for protein-free spreading. Binding of each protein was found to preserve an easily recognized configuration in the RNA that allows the sites of protein binding to be determined. S8--16S RNA complexes have a single hairpin loop near the middle of the 16S RNA, 798 +/- 21 bases from one end and 657 +/- 26 bases from the other. S4-16S RNA complexes have two adjacent loops at one end with 250--450 bases. This structure probably arises from the simultaneous binding of S4 to three noncontiguous sites on the RNA. Measurements of these complexes place the binding sites near the 5' end, at more than one site 250--585 nucleotides from the 5' end and 645 +/- 45 bases from the 3' end. The latter site has not been recognized previously as a distinct S4 binding site. This approach allows the binding sites to be determined without knowledge of the nucleotide sequence and gives insight into the configuration of the rRNA in the assembling ribisome.

摘要

特定复合物。利用电子显微镜对大肠杆菌核糖体组装早期的复合物进行了检测。核糖体蛋白S4或S8与16S RNA之间的复合物先用甲醛温和固定,然后变性以便进行无蛋白铺展。发现每种蛋白质的结合在RNA中保留了一种易于识别的构型,从而能够确定蛋白质的结合位点。S8 - 16S RNA复合物在16S RNA中部附近有一个单发卡环,从一端起798 ± 21个碱基,从另一端起657 ± 26个碱基。S4 - 16S RNA复合物在一端有两个相邻的环,含250 - 450个碱基。这种结构可能源于S4同时与RNA上三个不相邻的位点结合。对这些复合物的测量将结合位点定位在5'端附近,在距离5'端250 - 585个核苷酸且距离3'端645 ± 45个碱基的多个位点处。后一个位点以前未被识别为一个独特的S4结合位点。这种方法无需了解核苷酸序列就能确定结合位点,并能深入了解组装中的核糖体中rRNA的构型。

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