Unknown

Dataset Information

0

Dual-Color Photoconvertible Fluorescent Probes Based on Directed Photooxidation Induced Conversion for Bioimaging.


ABSTRACT: We herein present a new concept to produce dual-color photoconvertible probes based on a mechanism called Directed Photooxidation Induced Conversion (DPIC). As a support of this mechanism, styryl-coumarins (SCs) bearing Aromatic Singlet Oxygen Reactive Moieties (ASORMs) like furan and pyrrole have been synthesized. SCs are bright fluorophores, which undergo a hypsochromic conversion upon visible light irradiation due to directed photooxidation of the ASORM that leads to the disruption of conjugation. SC-P, a yellow emitting probe bearing a pyrrole moiety, converts to a stable blue emitting coumarin with a 68 nm shift allowing the photoconversion and tracking of lipid droplet in live cells. This new approach might pave the way to a new generation of photoconvertible dyes for advanced bioimaging applications.

SUBMITTER: Saladin L 

PROVIDER: S-EPMC10107923 | biostudies-literature | 2023 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

Dual-Color Photoconvertible Fluorescent Probes Based on Directed Photooxidation Induced Conversion for Bioimaging.

Saladin Lazare L   Breton Victor V   Dal Pra Ophélie O   Klymchenko Andrey S AS   Danglot Lydia L   Didier Pascal P   Collot Mayeul M  

Angewandte Chemie (International ed. in English) 20221214 4


We herein present a new concept to produce dual-color photoconvertible probes based on a mechanism called Directed Photooxidation Induced Conversion (DPIC). As a support of this mechanism, styryl-coumarins (SCs) bearing Aromatic Singlet Oxygen Reactive Moieties (ASORMs) like furan and pyrrole have been synthesized. SCs are bright fluorophores, which undergo a hypsochromic conversion upon visible light irradiation due to directed photooxidation of the ASORM that leads to the disruption of conjuga  ...[more]

Similar Datasets

| S-EPMC3600594 | biostudies-literature
| S-EPMC4268305 | biostudies-literature
| S-EPMC9104182 | biostudies-literature
| S-EPMC10501358 | biostudies-literature
| S-EPMC3673728 | biostudies-literature
| S-EPMC5597305 | biostudies-literature
| S-EPMC5773255 | biostudies-literature
| S-EPMC6688561 | biostudies-literature
| S-EPMC5485888 | biostudies-literature