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巴龙霉素结合会诱导16S rRNA的A位点发生局部构象变化。

Paromomycin binding induces a local conformational change in the A-site of 16 S rRNA.

作者信息

Fourmy D, Yoshizawa S, Puglisi J D

机构信息

Center for Molecular Biology of RNA, University of California, Santa Cruz, CA 95064, USA.

出版信息

J Mol Biol. 1998 Mar 27;277(2):333-45. doi: 10.1006/jmbi.1997.1551.

Abstract

Aminoglycoside antibiotics that bind to ribosomal RNA in the aminoacyl-tRNA site (A-site) cause misreading of the genetic code and inhibit translocation. An A-site RNA oligonucleotide specifically binds to aminoglycoside antibiotics and the structure of the RNA-paromomycin complex was previously determined by nuclear magnetic resonance (NMR) spectroscopy. Here, the A-site RNA structure in its free form has been determined using heteronuclear NMR and compared to the structure of the paromomycin-RNA complex. As in the complex with paromomycin, the asymmetric internal loop is closed by a Watson-Crick base-pair (C1407.G1494) and by two non-canonical base-pairs (U1406.U1495, A1408.A1493). A1492 stacks below A1493 and is intercalated between the upper and lower stems. The comparison of the free and bound conformations of the RNA shows that two universally conserved residues of the A site of 16 S rRNA, A1492 and A1493, are displaced towards the minor groove of the RNA helix in presence of antibiotic. These changes in the RNA conformation place the N1 positions of A1492 and A1493 on the minor groove side of the A-site RNA and suggest a mechanism of action of aminoglycosides on translation.

摘要

与氨酰 - tRNA位点(A位点)的核糖体RNA结合的氨基糖苷类抗生素会导致遗传密码错读并抑制转位。一种A位点RNA寡核苷酸特异性结合氨基糖苷类抗生素,并且先前已通过核磁共振(NMR)光谱法确定了RNA - 巴龙霉素复合物的结构。在这里,已使用异核NMR确定了其游离形式的A位点RNA结构,并与巴龙霉素 - RNA复合物的结构进行了比较。与和巴龙霉素形成的复合物一样,不对称内环由一个沃森 - 克里克碱基对(C1407.G1494)和两个非经典碱基对(U1406.U1495,A1408.A1493)封闭。A1492堆积在A1493下方,并插入上下茎之间。RNA游离和结合构象的比较表明,在存在抗生素的情况下,16 S rRNA的A位点的两个普遍保守残基A1492和A1493向RNA螺旋的小沟方向移位。RNA构象的这些变化使A1492和A1493的N1位置位于A位点RNA的小沟侧,并提示了氨基糖苷类抗生素对翻译的作用机制。

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