Julolidine-based small molecular probes for fluorescence imaging of RNA in live cells

0576478 - ÚOCHB 2024 RIV GB eng J - Journal Article
Mondal, I. C. - Rawat, P. - Galkin, Maksym - Deka, S. - Karmakar, A. - Mondal, P. - Ghosh, S.
Julolidine-based small molecular probes for fluorescence imaging of RNA in live cells.
Organic & Biomolecular Chemistry. Roč. 21, č. 38 (2023), s. 7831-7840. ISSN 1477-0520. E-ISSN 1477-0539
Institutional support: RVO:61388963
Keywords : aggregation-induced emission * graphene quantum dots * living cells
OECD category: Organic chemistry
Impact factor: 3.2, year: 2022
Method of publishing: Limited access
https://doi.org/10.1039/D3OB01314F

Intracellular RNA imaging with organic small molecular probes has been an intense topic, although the number of such reported dyes, particularly dyes with high quantum yields and long wavelength excitation/emission, is quite limited. The present work reports the design and synthesis of three cationic julolidine-azolium conjugates (OX-JLD, BTZ-JLD and SEZ-JLD) as turn-on fluorescent probes with appreciably high quantum yields and brightness upon interaction with RNA. A structure-efficiency relationship has been established for their potential for the interaction and imaging of intracellular RNA. Given their chemical structure, the free rotation between the donor and the acceptor gets restricted when the probes bind with RNA resulting in strong fluorescence emission towards a higher wavelength upon photoexcitation. A detailed investigation revealed that the photophysical properties and the optical responses of two probes, viz. BTZ-JLD and SEZ-JLD, towards RNA are very promising and qualify them to be suitable candidates for biological studies, particularly for cellular imaging applications. The probes allow imaging of intracellular RNA with prominent staining of nucleoli in live cells under a range of physiological conditions. The results of the cellular digest test established the appreciable RNA selectivity of BTZ-JLD and SEZ-JLD inside the cellular environment. Moreover, a comparison between the relative intensity profile of SEZ-JLD before and after the RNA-digestion test inside the cellular environment indicated that the interference of cellular viscosity in fluorescence enhancement is insignificant, and hence, SEZ-JLD can be used as a cell membrane permeable cationic molecular probe for deep-red imaging of intracellular RNA with a good degree of selectivity.
Permanent Link: https://hdl.handle.net/11104/0346040


Research data: CCDC