Molecular mechanisms and kinetics between DNA and DNA binding ligands

被引:145
作者
Sischka, A
Toensing, K
Eckel, R
Wilking, SD
Sewald, N
Ros, R
Anselmetti, D
机构
[1] Univ Bielefeld, Fak Phys, Dept Phys, D-33615 Bielefeld, Germany
[2] Univ Bielefeld, Dept Chem, D-33615 Bielefeld, Germany
关键词
D O I
10.1529/biophysj.103.036293
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Mechanical properties of single double-stranded DNA ( dsDNA) in the presence of different binding ligands were analyzed in optical-tweezers experiments with subpiconewton force resolution. The binding of ligands to DNA changes the overall mechanic response of the dsDNA molecule. This fundamental property can be used for discrimination and identification of different binding modes and, furthermore, may be relevant for various processes like nucleosome packing or applications like cancer therapy. We compared the effects of the minor groove binder distamycin-A, a major groove binding alpha-helical peptide, the intercalators ethidium bromide, YO-1, and daunomycin as well as the bisintercalator YOYO-1 on lambda-DNA. Binding of molecules to the minor and major groove of dsDNA induces distinct changes in the molecular elasticity compared to the free dsDNA detectable as a shift of the overstretching transition to higher forces. Intercalating molecules affect the molecular mechanics by a complete disappearance of the B-S transition and an associated increase in molecular contour length. Significant force hysteresis effects occurring during stretching/relaxation cycles with velocities >10 nm/s for YOYO-1 and >1000 nm/s for daunomycin. These indicate structural changes in the timescale of minutes for the YOYO-DNA and of seconds for the daunomycin-DNA complexes, respectively.
引用
收藏
页码:404 / 411
页数:8
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