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Excited-state locked amino analogues of the green fluorescent protein chromophore with a giant Stokes shift.


ABSTRACT: We design a novel class of excited-state locked GFP chromophores by introducing an amine group at the double exo-bond and a difluoroboryl bridge. We show that these chromophores intrinsically exhibit a very large Stokes shift of 1 eV. Further tuning through chemical modifications of their aryl substituents makes them environmentally sensitive.

SUBMITTER: Zaitseva SO 

PROVIDER: S-EPMC9076007 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature

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Excited-state locked amino analogues of the green fluorescent protein chromophore with a giant Stokes shift.

Zaitseva Snizhana O SO   Farkhutdinova Dilara A DA   Baleeva Nadezhda S NS   Smirnov Alexander Yu AY   Zagudaylova Marina B MB   Shakhov Aleksander M AM   Astafiev Artyom A AA   Baranov Mikhail S MS   Bochenkova Anastasia V AV  

RSC advances 20191126 66


We design a novel class of excited-state locked GFP chromophores by introducing an amine group at the double <i>exo</i>-bond and a difluoroboryl bridge. We show that these chromophores intrinsically exhibit a very large Stokes shift of 1 eV. Further tuning through chemical modifications of their aryl substituents makes them environmentally sensitive. ...[more]

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