Strauss-Soukup J K, Rodrigues P D, Maher L J
Department of Biochemistry and Molecular Biology and Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE 68198, USA.
Biophys Chem. 1998 Jun 9;72(3):297-306. doi: 10.1016/s0301-4622(98)00112-4.
Of the many forces involved in DNA bending by proteins, we have focused on the possible role of asymmetric phosphate neutralization due to interactions between the negatively charged phosphate backbone of duplex DNA and cationic amino acids of an approaching protein. The resulting unbalanced charge distribution along the duplex DNA is thought to induce the double helix to collapse toward the neutralized surface. Previous work has confirmed that DNA bending (approximately 20.7 +/- 4 degrees) is induced by asymmetric incorporation of six uncharged racemic methylphosphonate analogs partially neutralizing one face of GC-rich duplex DNA. We have now analyzed DNA duplexes with similar patches of methylphosphonate linkages in an AT-rich sequence context and again observe bending toward the neutralized face, to an extent (20 +/- 0.6 degrees) comparable to that observed for neutral patches in GC-rich DNA. The similar induced bend angles in AT-rich and GC-rich contexts does not reveal increased flexibility in AT-rich sequences, or a particular propensity of A-T base pairs to roll toward the minor groove in the tested sequences.
在蛋白质使DNA弯曲所涉及的众多作用力中,我们重点关注了由于双链DNA带负电荷的磷酸骨架与靠近的蛋白质的阳离子氨基酸之间的相互作用而导致的不对称磷酸中和的可能作用。沿双链DNA产生的不平衡电荷分布被认为会促使双螺旋向中和表面坍塌。先前的研究证实,通过不对称掺入六个不带电荷的外消旋甲基膦酸酯类似物部分中和富含GC的双链DNA的一个面,可诱导DNA弯曲(约20.7±4度)。我们现在分析了在富含AT的序列背景下具有类似甲基膦酸酯连接片段的DNA双链体,再次观察到向中和面的弯曲,弯曲程度(20±0.6度)与在富含GC的DNA中观察到的中性片段相当。在富含AT和富含GC的背景下相似的诱导弯曲角度并未显示出富含AT的序列具有更高的灵活性,也未显示出在测试序列中A - T碱基对向小沟滚动的特定倾向。