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大肠杆菌5S RNA的A和B构象体。通过酶法和化学方法进行表征。

Escherichia coli 5S RNA A and B conformers. Characterisation by enzymatic and chemical methods.

作者信息

Göringer H U, Szymkowiak C, Wagner R

出版信息

Eur J Biochem. 1984 Oct 1;144(1):25-34. doi: 10.1111/j.1432-1033.1984.tb08426.x.

Abstract

The structures of the two stable conformers of Escherichia coli 5 S RNA, the and B form, were compared. Information about the structures were obtained using the methods of limited enzymatic hydrolysis and chemical modification of accessible nucleotides. Base-specific modifications were performed for adenosines and cytidines using diethylpyrocarbonate and dimethylsulfate in combination with a strand-scission reaction at the modified site. Base-specific (RNase T1) as well as conformation-specific (nuclease S1, cobra venom nuclease) enzymes were employed for the limited enzymatic hydrolysis. Clear differences in the accessibility of the two 5 S RNA conformers to the enzymes and the chemical reagents were established and the regions with altered reactivities were localized in the 5 S RNA structure. The results are consistent with the disruption of the secondary structural interactions in helix II and partly in helices III and IV during the transition from the A to the B form. (The numbering of the helices is according to the generally accepted Fox and Woese model.) In addition some regions presumably involved in the tertiary structure are distorted. There is evidence, however, for the new formation of structural regions between two distant sites in the 5 S RNA B form. The results enable us to refine the existing 5 S RNA A-form model and provide insight into the structural dynamics that lead to the formation of the 5 S RNA B form.

摘要

对大肠杆菌5S RNA的两种稳定构象(即A构象和B构象)的结构进行了比较。通过有限酶促水解和可及核苷酸化学修饰的方法获得了有关结构的信息。使用焦碳酸二乙酯和硫酸二甲酯对腺苷和胞苷进行碱基特异性修饰,并结合在修饰位点的链断裂反应。使用碱基特异性(核糖核酸酶T1)以及构象特异性(核酸酶S1、眼镜蛇毒核酸酶)酶进行有限酶促水解。确定了两种5S RNA构象对酶和化学试剂的可及性存在明显差异,并将反应性改变的区域定位在5S RNA结构中。结果与从A构象向B构象转变过程中螺旋II以及部分螺旋III和IV中的二级结构相互作用的破坏一致。(螺旋的编号根据普遍接受的福克斯和沃斯模型。)此外,一些可能参与三级结构的区域也发生了扭曲。然而,有证据表明在5S RNA B构象的两个远距离位点之间形成了新的结构区域。这些结果使我们能够完善现有的5S RNA A构象模型,并深入了解导致5S RNA B构象形成的结构动力学。

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