Suppr超能文献

II类氨酰-tRNA合成酶的剖析:小螺旋识别的决定因素与氨基酸活化结构域紧密相关。

Dissection of a class II tRNA synthetase: determinants for minihelix recognition are tightly associated with domain for amino acid activation.

作者信息

Buechter D D, Schimmel P

机构信息

Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.

出版信息

Biochemistry. 1993 May 18;32(19):5267-72. doi: 10.1021/bi00070a039.

Abstract

The ten class II aminoacyl-tRNA synthetases are large homo- and hetero-oligomeric proteins that share three conserved sequence motifs. Within this class, Escherichia coli alanyl-tRNA synthetase is the only homotetramer and is comprised of subunits of 875 amino acids. The enzyme aminoacylates sequence-specific RNA oligonucleotides that recreate as few as four base pairs of the acceptor stem of tRNA(Ala). A monomeric 461 amino acid N-terminal fragment (461N) was previously shown to have full adenylate synthesis activity. However, fragment 461N has significant, but reduced, efficiency of charging of tRNA(Ala), when compared to native enzyme [Ho, C., Jasin, M., & Schimmel, P. (1985) Science 229, 389-393]. We show here that, in contrast, the fragment and the native enzyme aminoacylate a 12 base pair acceptor-T psi C stem minihelix and a four base pair RNA tetraloop with the same efficiency. We also show that fragment 461N makes footprint contacts both on and outside the acceptor helix of bound tRNA(Ala). With one possible exception, the contacts observed with fragment 461N are identical to those seen with the native enzyme. In spite of contacts outside the acceptor helix, fragment 461N charges the native tRNA, minihelix, and tetraloop with similar efficiency. Thus, all minihelix contacts required for activation for charging are tightly associated with the adenylate synthesis domain and, at least in the fragment, are not influenced by additional RNA-protein contacts outside the minihelix domain.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

十种II类氨酰-tRNA合成酶是大型的同源和异源寡聚蛋白,它们共有三个保守的序列基序。在这一类中,大肠杆菌丙氨酰-tRNA合成酶是唯一的同四聚体,由875个氨基酸的亚基组成。该酶对序列特异性RNA寡核苷酸进行氨酰化,这些寡核苷酸可重现tRNA(Ala)接受茎的少至四个碱基对。先前已证明一个461个氨基酸的单体N端片段(461N)具有完整的腺苷酸合成活性。然而,与天然酶相比,片段461N对tRNA(Ala)的充电效率显著降低,但仍有一定活性[Ho,C.,Jasin,M.,& Schimmel,P.(1985)Science 229,389 - 393]。我们在此表明,相比之下,该片段和天然酶对一个12个碱基对的接受体-TψC茎小螺旋和一个4个碱基对的RNA四环进行氨酰化的效率相同。我们还表明,片段461N在结合的tRNA(Ala)的接受体螺旋上和外部都形成足迹接触。除了一个可能的例外,片段461N观察到的接触与天然酶的接触相同。尽管在接受体螺旋外部有接触,片段461N对天然tRNA、小螺旋和四环的充电效率相似。因此,充电激活所需的所有小螺旋接触都与腺苷酸合成结构域紧密相关,并且至少在该片段中,不受小螺旋结构域外部额外的RNA - 蛋白质接触的影响。(摘要截短至250字)

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验