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丙型肝炎病毒内部核糖体进入位点的发夹IIIe周围的蛋白质,位于人40S核糖体亚基上。

Proteins surrounding hairpin IIIe of the hepatitis C virus internal ribosome entry site on the human 40S ribosomal subunit.

作者信息

Laletina Elena, Graifer Dmitri, Malygin Alexey, Ivanov Anton, Shatsky Ivan, Karpova Galina

机构信息

Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, 630090, Russia.

出版信息

Nucleic Acids Res. 2006 Apr 13;34(7):2027-36. doi: 10.1093/nar/gkl155. Print 2006.

Abstract

Binding of the internal ribosome entry site (IRES) of the hepatitis C virus (HCV) RNA to the eIF-free 40S ribosomal subunit is the first step of initiation of translation of the viral RNA. Hairpins IIId and IIIe comprising 253-302 nt of the IRES are known to be essential for binding to the 40S subunit. Here we have examined the molecular environment of the HCV IRES in its binary complex with the human 40S ribosomal subunit. For this purpose, two RNA derivatives were used that bore a photoactivatable perfluorophenyl azide cross-linker. In one derivative the cross-linker was at the nucleotide A296 in hairpin IIIe, and in the other at G87 in domain II. Site-specific introduction of the cross-linker was performed using alkylating derivatives of oligodeoxyribonucleotides complementary to the target RNA sequences. No cross-links with the rRNA were detected with either RNA derivative. The RNA with the photoactivatable group at A296 cross-linked to proteins identified as S5 and S16 (major) and p40 and S3a (minor), while no cross-links with proteins were detected with RNA modified at G87. The results obtained indicate that hairpin IIIe is located on the solvent side of the 40S subunit head on a site opposite the beak.

摘要

丙型肝炎病毒(HCV)RNA的内部核糖体进入位点(IRES)与无eIF的40S核糖体亚基结合是病毒RNA翻译起始的第一步。已知包含IRES的253 - 302 nt的发夹IIId和IIIe对于与40S亚基的结合至关重要。在此,我们研究了HCV IRES与人类40S核糖体亚基二元复合物中的分子环境。为此,使用了两种带有可光活化全氟苯基叠氮交联剂的RNA衍生物。在一种衍生物中,交联剂位于发夹IIIe中的核苷酸A296处,另一种位于结构域II中的G87处。使用与靶RNA序列互补的寡脱氧核糖核苷酸的烷基化衍生物进行交联剂的位点特异性引入。两种RNA衍生物均未检测到与rRNA的交联。在A296处带有可光活化基团的RNA与鉴定为S5和S16(主要)以及p40和S3a(次要)的蛋白质交联,而在G87处修饰的RNA未检测到与蛋白质的交联。所得结果表明,发夹IIIe位于40S亚基头部的溶剂侧,喙的对面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a24/1435985/a7c8105ae706/gkl155f1.jpg

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