DNA bending by asymmetrically tethered cations: influence of tether flexibility

被引:20
作者
Hardwidge, PR
Lee, DK
Prakash, TP
Iglesias, B
Den, RB
Switzer, C [1 ]
Maher, LJ
机构
[1] Mayo Clin & Mayo Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
来源
CHEMISTRY & BIOLOGY | 2001年 / 8卷 / 10期
关键词
DNA bending; DNA curvature; electrophoresis; cations; asymmetric neutralization; phosphate; base analogs;
D O I
10.1016/S1074-5521(01)00065-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: We have been studying the proposal that laterally asymmetric charge neutralization along the DNA double helix can induce collapse toward the neutralized surface. Results of previous experiments implied that such a phenomenon can occur, suggesting a role for local interphosphate repulsive forces in DNA shape and rigidity. Results: We now show that, whereas six ammonium ions tethered to one DNA face on flexible propyl chains can induce detectable DNA curvature, tethering of ammonium ions on rigid propynyl tethers does not induce DNA curvature. Molecular modeling indicates differing propensities for phosphate salt bridge formation between propyl- and propynyl-tethered ammonium ions. Conclusions: Ammonium ion localization is suggested as a key factor in induced bending. Rigidification of the double helix by stacking of propyne groups cannot be excluded. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:967 / 980
页数:14
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