Kinetic studies on acridine orange-DNA interaction. A branched mechanism involving intercalation and outside "dimerization".
Kinetic studies on acridine orange-DNA interaction. A branched mechanism involving intercalation and outside "dimerization".
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吖啶橙-DNA相互作用的动力学研究。
DOI:
10.1093/oxfordjournals.jbchem.a129839
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发表时间:
1972
期刊:
影响因子:
--
通讯作者:
K. Akasaka
中科院分区:
文献类型:
--
作者:
M. Sakoda;K. Hiromi;K. Akasaka
The fluorescence stopped-flow technique was applied to kinetic studies on the acridine orange (AO)-DNA interaction. The dynamic process of “dimerization“ of AO on the outside of DNA as well as the process of intercalation was directly followed with this technique. The concentration dependence of the relaxation time τ of each process suggests that both of them are essentially unimolecular processes preceded by a rapid pre-equilibrium of bimolecular nature, which is considered to be a random binding of AO molecules to the outside phosphate groups of DNA. This confirmed. our earlier suggestion of a branched mechanism of interaction: where (AO)xdenotes the bound state ot AO molecule specified by the subscriptx. In addition, a remarkable decrease of 1/τ for dimerization with theP/Dratio was observed. This result suggests that the observed dimerization is brought about by a rearrangement of randomly bound AO molecules, which may be regarded as a one dimensional random walk of AO monomers in an electrostatic potential trough formed by the regular array of DNA-phosphates. On the other hand, a decrease of 1/τ with decreasingP/Dratio was observed for intercalation, which indicates that the process of intercalation is considerably retarded by the presence of bound dimers at lowP/Dratios.