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Selective recognition of ATP by multivalent nano-assemblies of bisimidazolium amphiphiles through "turn-on" fluorescence response.


ABSTRACT: Bisimidazolium receptors, tagged with chromophoric pyrene at one end and linked to an n-alkyl chain at the other, underwent self-assembly in aqueous media depending on the length of the alkyl segment. The amphiphilic derivatives having n-decyl or longer chains, formed nano-assemblies with cyanic-green emission resulting from the stacked pyrene chromophores in the aggregates. The presence of positive surface charges on the multivalent aggregates led to ATP binding which was accompanied by a significant increase in the excimeric emission intensity. This provided a convenient way of monitoring ATP binding in a "turn-on" mode and an efficient detection of ATP was achieved in aqueous buffer and also in buffer containing 150 mM NaCl at physiological pH value. Furthermore, the multivalent aggregates demonstrated a significant selectivity in ATP detection over ADP, AMP and pyrophosphate.

SUBMITTER: Biswas R 

PROVIDER: S-EPMC7670119 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

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Selective recognition of ATP by multivalent nano-assemblies of bisimidazolium amphiphiles through "turn-on" fluorescence response.

Biswas Rakesh R   Ghosh Surya S   Bhaumik Shubhra Kanti SK   Banerjee Supratim S  

Beilstein journal of organic chemistry 20201110


Bisimidazolium receptors, tagged with chromophoric pyrene at one end and linked to an <i>n</i>-alkyl chain at the other, underwent self-assembly in aqueous media depending on the length of the alkyl segment. The amphiphilic derivatives having <i>n</i>-decyl or longer chains, formed nano-assemblies with cyanic-green emission resulting from the stacked pyrene chromophores in the aggregates. The presence of positive surface charges on the multivalent aggregates led to ATP binding which was accompan  ...[more]

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