A Bodipy (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) derivative has been conceived and synthesized starting from L-aspartic acid, as a selective turn-off sensor of Cu2 + ions. Its acid–base properties were determined to study the formation of metal/sensor complex species by titration of solutions each containing a different metal ion, such as Cu2 +, Ca2 +, Zn2 +, Pb2 + and Hg2 + and different metal/sensor ratios. The speciation models allowed us to simulate the distribution of the metal/sensor complex species at the normal concentrations of the corresponding metals present in biological fluids. The distribution diagrams, obtained by varying the concentration of sensor 1, clearly indicate that sensor 1 responds selectively to Cu2 + at micromolar concentrations, even in the presence of other more abundant metal cations Ca2 +. Finally, we analyzed the cellular uptake of sensor 1 on human erythrocytes and its ability to chelate Cu2 + in the cellular environment. Results indicate that it crosses the plasmatic membrane and colors the cells of a bright fluorescent red. Exposing the fluorescent cells to Cu2 + results in a complete cellular photobleaching of the red fluorescence, indicating that sensor 1 is able to detect metal changes in the cytosolic environment.

Sequestering ability to Cu2 + of a new bodipy-based dye and its behavior as in vitro fluorescent sensor

PAPALIA, teresa;BARATTUCCI, Anna;BARRECA, Davide;BELLOCCO, Ersilia Santa;BONACCORSI, Paola Maria;NICOLO', MARCO SEBASTIANO;FOTI, Claudia
2017-01-01

Abstract

A Bodipy (4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) derivative has been conceived and synthesized starting from L-aspartic acid, as a selective turn-off sensor of Cu2 + ions. Its acid–base properties were determined to study the formation of metal/sensor complex species by titration of solutions each containing a different metal ion, such as Cu2 +, Ca2 +, Zn2 +, Pb2 + and Hg2 + and different metal/sensor ratios. The speciation models allowed us to simulate the distribution of the metal/sensor complex species at the normal concentrations of the corresponding metals present in biological fluids. The distribution diagrams, obtained by varying the concentration of sensor 1, clearly indicate that sensor 1 responds selectively to Cu2 + at micromolar concentrations, even in the presence of other more abundant metal cations Ca2 +. Finally, we analyzed the cellular uptake of sensor 1 on human erythrocytes and its ability to chelate Cu2 + in the cellular environment. Results indicate that it crosses the plasmatic membrane and colors the cells of a bright fluorescent red. Exposing the fluorescent cells to Cu2 + results in a complete cellular photobleaching of the red fluorescence, indicating that sensor 1 is able to detect metal changes in the cytosolic environment.
2017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3104866
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