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通过拉曼光谱和红外光谱对G.U摆动碱基对的证明。

Demonstration of G . U wobble base pairs by Raman and IR spectroscopy.

作者信息

Ackermann T, Gramlich V, Klump H, Knäble T, Schmid E D, Seliger H, Stulz J

机构信息

Inst. Physik. Chemie, Universität Freiburg, W. Germany.

出版信息

Biophys Chem. 1979 Nov;10(3-4):231-8. doi: 10.1016/0301-4622(79)85011-5.

Abstract

When guanine and uracil form hydrogen bonds in the pairing scheme first proposed by Crick one would expect that poly(A,G) will form an unperturbed double helix with poly U at room temperature in a dilute electrolyte solution (0.1 M NaCl). We have demonstrated by Raman- and IR-spectroscopy that the secondary structure of poly(A.G) . poly U is very similar to the structure of poly A . poly U; only the thermal stability of the double helix seems slightly lower than the stability of poly A . poly U, whereas the average helix length is unaffected by the dispersed G . U base pairs. From our input ratio of guanine and adenine we estimate that about every fourth base pair is a wobble pair.

摘要

当鸟嘌呤和尿嘧啶按照克里克最初提出的配对方案形成氢键时,可以预期聚(A,G)在室温下于稀电解质溶液(0.1M氯化钠)中会与聚U形成未受干扰的双螺旋结构。我们通过拉曼光谱和红外光谱证明,聚(A,G)·聚U的二级结构与聚A·聚U的结构非常相似;只是双螺旋的热稳定性似乎略低于聚A·聚U的稳定性,而平均螺旋长度不受分散的G·U碱基对的影响。根据我们鸟嘌呤和腺嘌呤的输入比例,我们估计大约每四个碱基对中有一个摆动对。

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