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DNA的序列特异性识别:合成RNA聚合酶启动子亚氨基质子的核磁共振研究

Sequence-specific recognition of DNA: NMR studies of the imino protons of a synthetic RNA polymerase promoter.

作者信息

Chou S H, Wemmer D E, Hare D R, Reid B R

出版信息

Biochemistry. 1984 May 8;23(10):2257-62. doi: 10.1021/bi00305a026.

Abstract

We have synthesized both strands of a DNA duplex containing the consensus Pribnow promoter sequence TATAATG , flanked by GC base pairs to stabilize the ends of the helix. The stability of this duplex has been studied by using 1H nuclear magnetic resonance. The imino protons have been assigned by using the sequential nuclear Overhauser effect approach. Exchange rates have been monitored by using selective inversion recovery measurements. The helix is relatively unstable in the center of the AT-rich region even when surrounded by GC base pairs, and there is considerable asymmetry in the melting of the helix.

摘要

我们合成了包含共有普里布诺启动子序列TATAATG的DNA双链体的两条链,其两侧为GC碱基对以稳定螺旋末端。通过使用1H核磁共振研究了该双链体的稳定性。利用序列核Overhauser效应方法对亚氨基质子进行了归属。通过选择性反转恢复测量监测了交换速率。即使被GC碱基对包围,该螺旋在富含AT区域的中心也相对不稳定,并且螺旋解链存在相当大的不对称性。

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