Highly Hydrophilic, Two-photon Fluorescent Terpyridine Derivatives Containing Quaternary Ammonium for Specific Recognizing Ribosome RNA in Living Cells
Source abstract
Abstract
A two-photon fluorescent probe (J1) that selectively stains intracellular nucleolar RNA was screened from three water-soluble terpyridine derivatives (J1-J3) with quaternary ammonium groups. The photophysical properties of J1-J3 were systemically investigated both experimentally and theoretically, revealing that J1-J3 possess large Stokes shifts and the two-photon absorption action cross sections range from 38 to 97 GM in the near-infrared region. This indicates that J1 could specifically stain nucleoli by targeting the nucleolar rRNA from the recognition experiments in vitro, the two-photon imaging experiments, and the stimulated emission depletion in vivo. The mechanism of action in which J1 binds to the nucleolar rRNA was researched via both experiments and molecular modeling. The high binding selectivity of J1 to nucleolar RNA over cytosolic RNA made this probe a potential candidate to visualize rRNA probe in the living cells.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced biosensing and bioanalysis techniques · RNA Interference and Gene Delivery · DNA and Nucleic Acid Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, University College London, London WC1H 0AJ, U.K.
School of Chemistry and Chemical Engineering, Huangshan College, Huangshan University, Huangshan 245041, P. R. China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Anhui Province · 2017 Returnees innovation and entrepreneurship key support program · Anhui University Doctor Startup Fund · The Higher Education Revitalization Plan Talent Project (2013)
References (37)
Show source-provided references
1. 10.1126/science.aad280810.1126/science.aad2808 ↗
2. 10.1016/j.biomaterials.2016.04.02610.1016/j.biomaterials.2016.04.026 ↗
3. 10.1039/C6SC01589A10.1039/C6SC01589A ↗
4. 10.1039/C5TB02474A10.1039/C5TB02474A ↗
5. 10.1039/C6TB00319B10.1039/C6TB00319B ↗
6. 10.1021/jacs.5b0145110.1021/jacs.5b01451 ↗
7. 10.1039/C5CC07124K10.1039/C5CC07124K ↗
8. 10.1126/science.106008910.1126/science.1060089 ↗
9. 10.1021/acsami.6b1073710.1021/acsami.6b10737 ↗
10. 10.1016/j.bios.2014.12.05510.1016/j.bios.2014.12.055 ↗
11. 10.1021/ja800892410.1021/ja8008924 ↗
12. 10.1039/C5CC05551B10.1039/C5CC05551B ↗
13. 10.1016/j.biomaterials.2013.11.05210.1016/j.biomaterials.2013.11.052 ↗
14. 10.1038/nprot.2006.48410.1038/nprot.2006.484 ↗
15. 10.1021/ja056303g10.1021/ja056303g ↗
16. 10.1021/cr500442510.1021/cr5004425 ↗
17. 10.1021/ja404422z10.1021/ja404422z ↗
18. 10.1016/j.biomaterials.2015.02.10610.1016/j.biomaterials.2015.02.106 ↗
19. 10.1021/acsami.6b1246910.1021/acsami.6b12469 ↗
20. 10.1021/acsami.6b0325910.1021/acsami.6b03259 ↗
21. 10.1021/acsami.5b0853910.1021/acsami.5b08539 ↗
22. 10.1039/C5SC03956H10.1039/C5SC03956H ↗
23. 10.1021/jacs.6b0162510.1021/jacs.6b01625 ↗
24. 10.1021/cb500927r10.1021/cb500927r ↗
25. 10.1021/cr200359p10.1021/cr200359p ↗
26. 10.1016/j.biomaterials.2013.02.03210.1016/j.biomaterials.2013.02.032 ↗
27. 10.1021/ja311227410.1021/ja3112274 ↗
28. 10.1021/acs.accounts.6b0058310.1021/acs.accounts.6b00583 ↗
29. 10.1016/j.dyepig.2016.12.05210.1016/j.dyepig.2016.12.052 ↗
30. 10.1002/anie.20080525710.1002/anie.200805257 ↗
31. 10.1002/chem.20060068910.1002/chem.200600689 ↗
32. 10.1364/AO.37.00735210.1364/AO.37.007352 ↗
33. 10.1039/C6TB01202G10.1039/C6TB01202G ↗
34. 10.1016/j.dyepig.2016.09.02010.1016/j.dyepig.2016.09.020 ↗
35. 10.1039/c2ra22423b10.1039/c2ra22423b ↗
36. Weaver R. F. · 2011
37. 10.1126/science.aab350010.1126/science.aab3500 ↗