Progressive DNA bending is made possible by gradual changes in the torsion angle of the glycosyl bond

被引:9
作者
Pardo, L
Pastor, N
Weinstein, H
机构
[1] CUNY Mt Sinai Sch Med, Dept Physiol & Biophys, New York, NY 10029 USA
[2] Univ Autonoma Barcelona, Fac Med, Unidad Bioestadist, Lab Med Computac, Bellaterra 08193, Barcelona, Spain
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(98)77928-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Structural comparisons have led to the suggestion that the conformational rearrangement that would be required to change A-DNA into the TA-DNA form of DNA observed in the complex with the TATA box binding protein (TBP) could be completed by modifying only the value of the glycosyl bond chi by similar to 45 degrees. The lack of a high number of crystal structures of this type makes it difficult to conclude whether a smooth transition from A-DNA to TA-DNA can occur without disrupting at any point either the Watson-Crick base pairing or the A-DNA conformation of the backbone. To explore the possibility of such a smooth transition, constrained molecular dynamics simulations were carried out for the double-stranded dodecamer d(GGTATATAAAAC), in which a transition from A-DNA to TA-DNA was induced by modifying only the chi angle values. The results demonstrate the feasibility of a continuous path in the A-DNA to TA-DNA transition. Varying extents of DNA curvature are also attainable, by maintaining the A-DNA backbone structure and Watson-Crick hydrogen bonding while changing the chi angle value smoothly from that in A-DNA to one corresponding to B-DNA.
引用
收藏
页码:2191 / 2198
页数:8
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