菁
化学
合作性
单体
J-骨料
DNA
二聚体
结晶学
离子强度
骨料(复合)
生物物理学
分子
纳米技术
有机化学
生物化学
荧光
聚合物
水溶液
物理
材料科学
量子力学
生物
作者
Miaomiao Wang,Gloria L. Silva,Bruce A. Armitage
摘要
UV−vis and CD spectroscopy reveal that a tricationic cyanine dye spontaneously assembles into a helical J-aggregate in the presence of a double-helical DNA template. The stability of the J-aggregate is strongly dependent on the dye concentration and DNA length in a manner that reflects a high degree of cooperativity in formation of the aggregate. Slight changes in environmental conditions such as temperature and ionic strength result in interconversion between J- and H-aggregates. The aggregate likely consists of dimeric units assembled in an offset, face-to-face orientation within the minor groove of the DNA template, analogous to an earlier report of H-aggregation on DNA by a related cyanine dye. A model is proposed that relates the two aggregate structures by translation of one monomer from a given dimer along the floor of the minor groove. This translation requires adjacent monomers to also translate, leading to the observed cooperativity.
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