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机构地区:[1]Changchun Center of Mass Spectrometry,Changehun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun,Jilin 130022,China [2]Graduate School of the Chinese Academy of Sciences,Beijing 100039,China [3]Changchun University of Chinese Medicine,Changchun,Jilin 130117,China
出 处:《Chinese Journal of Chemistry》2012年第7期1433-1438,共6页中国化学(英文版)
基 金:Acknowledgement This work was supported by the National Natural Science Foundation of China (No. 28073137).
摘 要:In this study, electrospray ionization mass spectrometry (ESI-MS) was used to investigate interaction of 21 flavonoids (10 aglycones and 11 glycosides) with the parallel quadruplex structure [d(TGGGGT)]4. Relative binding affinities of flavonoids toward [d(TGGGGT)]4 were estimated based on the fraction of bound DNA. It was found that [d(TGGGGT)]4 showed a binding preference to the flavonoid glycosides over flavonoid aglycones. It was d duced that glycosylation played a key role for the [d(TGGGGT)]a-binding properties of flavonoid glycosides. Upon collision-induced dissociation, complexes of flavonoid/[d(TGGGGT)]4 underwent the loss of flavonoids, suggesting an end-stacking binding mode. The current work demonstrates that ESI-MS is a powerful tool in the study of irheraction between drugs and nucleic acids.In this study, electrospray ionization mass spectrometry (ESI-MS) was used to investigate interaction of 21 flavonoids (10 aglycones and 11 glycosides) with the parallel quadruplex structure [d(TGGGGT)]4. Relative binding affinities of flavonoids toward [d(TGGGGT)]4 were estimated based on the fraction of bound DNA. It was found that [d(TGGGGT)]4 showed a binding preference to the flavonoid glycosides over flavonoid aglycones. It was d duced that glycosylation played a key role for the [d(TGGGGT)]a-binding properties of flavonoid glycosides. Upon collision-induced dissociation, complexes of flavonoid/[d(TGGGGT)]4 underwent the loss of flavonoids, suggesting an end-stacking binding mode. The current work demonstrates that ESI-MS is a powerful tool in the study of irheraction between drugs and nucleic acids.
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