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Selective parallel G-quadruplex recognition by a NIR-to-NIR two-photon squaraine.


ABSTRACT: Fluorescence imaging probes for specific G-quadruplex (G4) conformations are of considerable interest in biomedical research. Herein, we present the synthesis and the binding properties of a new water-soluble near-infrared (NIR) amphiphilic squaraine dye (CAS-C1) which is capable of selective detection of parallel over non-parallel and non G4 topologies. The striking changes in its linear optical response upon binding to parallel G4s give rise to high fluorescence quantum yields (? f ? 0.7) and one-photon molecular brightness in the far-red-NIR region. The outstanding recognition process of CAS-C1 for parallel G4s via end-stacking provides binding constants in the nanomolar regime (K b = 107 to 108 M-1) awarding it as one of the most potent parallel G4 binders currently available. Moreover, the CAS-C1-parallel G4 system exhibits large two-photon absorption (TPA) cross-sections and molecular brightness in the second NIR biological transparency window (? ? 1275 nm), making it an ideal candidate for NIR-to-NIR ultrasensitive two-photon procedures.

SUBMITTER: Grande V 

PROVIDER: S-EPMC6240894 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Selective parallel G-quadruplex recognition by a NIR-to-NIR two-photon squaraine.

Grande Vincenzo V   Shen Chia-An CA   Deiana Marco M   Dudek Marta M   Olesiak-Banska Joanna J   Matczyszyn Katarzyna K   Würthner Frank F  

Chemical science 20180914 44


Fluorescence imaging probes for specific G-quadruplex (G4) conformations are of considerable interest in biomedical research. Herein, we present the synthesis and the binding properties of a new water-soluble near-infrared (NIR) amphiphilic squaraine dye (<b>CAS-C1</b>) which is capable of selective detection of parallel over non-parallel and non G4 topologies. The striking changes in its linear optical response upon binding to parallel G4s give rise to high fluorescence quantum yields (<i>Φ</i>  ...[more]

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