Reinert K E
Biophys Chem. 1981 Feb;13(1):1-14. doi: 10.1016/0301-4622(81)80019-1.
Distamycin A binds strongly/moderately to DNA below/above r = 0.08 molecules bound per DNA phosphate. Titration viscometric measurements for high and low molecular weight DNA yielded the relative changes of DNA persistence length, delta alpha/alpha 0, and contour length, delta L/L0 (Nucl. Acids Res. 7 (1979) 1375). delta L/L0 is negligible/positive in the range below/above r = 0.09 at 0.2 M Na+! A two-line covering of the small groove by ligand molecules explains the increase of contour length. The characteristic delta alpha/alpha 0 drop is quantitatively interpreted by local DNA bending (kinking). The underlying theoretical basis is presented in two appendices and applied, in a third one, to literature data for the DNA-actinomycin system. The angle gamma of local DNA bending as induced by complex formation with different distamycin derivatives is presented for DNA species of different base composition. By means of appropriate model, a length mismatch per dinucleotide of (0.03(2) +/- 0.01)nm [or (0.04(3) +/- 0.01)nm] was derived from the experimentally obtained bending angle per dinucleotide of (1.6 +/- 0.4)0 [or (2.1 +/- 0.05)0], independent of DNA base composition and distamycin chain length.
在每个DNA磷酸上结合的分子数r低于/高于0.08时,Distamycin A与DNA的结合为强/中度结合。对高分子量和低分子量DNA进行的滴定粘度测量得出了DNA持久长度的相对变化量δα/α0和轮廓长度的相对变化量δL/L0(《核酸研究》7 (1979) 1375)。在0.2 M Na+条件下,当r低于/高于0.09时,δL/L0可忽略不计/为正值!配体分子对小沟的双线覆盖解释了轮廓长度的增加。特征性的δα/α0下降通过局部DNA弯曲(扭结)得到了定量解释。两个附录中给出了其理论基础,并在第三个附录中将其应用于DNA-放线菌素系统的文献数据。针对不同碱基组成的DNA种类,给出了与不同Distamycin衍生物形成复合物所诱导的局部DNA弯曲角度γ。通过合适的模型,从实验得到的每个二核苷酸的弯曲角度(1.6±0.4)° [或(2.1±0.05)°]推导出每个二核苷酸的长度错配为(0.03(2)±0.01)nm [或(0.04(3)±0.01)nm],这与DNA碱基组成和Distamycin链长无关。