journal article·2018-04-25

Cationic Organochalcogen with Monomer/Excimer Emissions for Dual-Color Live Cell Imaging and Cell Damage Diagnosis

Xi-Juan Chao, Kang-Nan Wang, Li-Li Sun, Qian Cao, Zhuo-Feng Ke, Du-Xia Cao, Zong-Wan Mao

ACS Applied Materials & Interfaces· Volume 10· Issue 16
Publisher page

Abstract

Studies on the development of fluorescent organic molecules with different emission colors for imaging of organelles and their biomedical application are gaining lots of focus recently. Here, we report two cationic organochalcogens 1 and 2, both of which exhibit very weak green emission (Φ1 = 0.12%; Φ2 = 0.09%) in dilute solution as monomers, but remarkably enhanced green emission upon interaction with nucleic acids and large red-shifted emission in aggregate state by the formation of excimers at high concentration. More interestingly, the monomer emission and excimer-like emission can be used for dual color imaging of different organelles. Upon passively diffusing into cells, both probes selectively stain nucleoli with strong green emission upon 488 nm excitation, whereas upon 405 nm excitation, a completely different stain pattern by staining lysosomes (for 1) or mitochondria (for 2) with distinct red emission is observed because of the highly concentrated accumulation in these organelles. Studies on the mechanism of the accumulation in lysosomes (for 1) or mitochondria (for 2) found that the accumulations of the probes are dependent on the membrane permeabilization, which make the probes have great potential in diagnosing cell damage by sensing lysosomal or mitochondrial membrane permeabilization. The study is demonstrative, for the first time, of two cationic molecules for dual-color imaging nucleoli and lysosomes (1)/mitochondria (2) simultaneously in live cell based on monomer and excimer-like emission, respectively, and more importantly, for diagnosing cell damage.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Molecular Sensors and Ion Detection · Photochromic and Fluorescence Chemistry

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry, Sun Yat-Sen University, Guangzhou 510275, China

School of Materials Science and Engineering, University of Jinan, Jinan 250022 Shandong, China

College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China

Funding

Ministry of Science and Technology of the People's Republic of China · Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Guangdong Province · the Fundamental Research Funds for the Central Universities

References (60)

Show source-provided references
1. 10.1038/nrc143010.1038/nrc1430 ↗
2. 10.1002/anie.20140889710.1002/anie.201408897 ↗
3. 10.1126/science.106008910.1126/science.1060089 ↗
4. 10.1038/3501407810.1038/35014078 ↗
5. 10.1002/jcb.1073510.1002/jcb.10735 ↗
6. 10.1002/(sici)1096-9896(200006)191:2<181::aid-path607>3.0.co;2-v10.1002/(sici)1096-9896(200006)191:2<181::aid-path607>3.0.co;2-v ↗
7. 10.1038/onc.2008.31010.1038/onc.2008.310 ↗
8. 10.1038/nrm356510.1038/nrm3565 ↗
9. 10.1038/nrm243410.1038/nrm2434 ↗
10. 10.1021/ja310324q10.1021/ja310324q ↗
11. 10.1021/acs.analchem.5b0280710.1021/acs.analchem.5b02807 ↗
12. 10.1021/jacs.5b1042510.1021/jacs.5b10425 ↗
13. 10.1021/acsami.6b1073710.1021/acsami.6b10737 ↗
14. 10.1039/c6cc03746a10.1039/c6cc03746a ↗
15. 10.1016/j.biomaterials.2013.11.05210.1016/j.biomaterials.2013.11.052 ↗
16. 10.1021/cb500927r10.1021/cb500927r ↗
17. 10.1016/j.biomaterials.2013.05.02010.1016/j.biomaterials.2013.05.020 ↗
18. 10.1016/j.bios.2014.12.05510.1016/j.bios.2014.12.055 ↗
19. 10.1021/acsami.7b0457610.1021/acsami.7b04576 ↗
20. 10.1021/acs.analchem.5b0084710.1021/acs.analchem.5b00847 ↗
21. 10.1002/anie.20140574210.1002/anie.201405742 ↗
22. 10.1039/c6sc04322d10.1039/c6sc04322d ↗
23. 10.1039/c7sc03321d10.1039/c7sc03321d ↗
24. 10.1002/asia.20170034010.1002/asia.201700340 ↗
25. 10.1039/c6tb00319b10.1039/c6tb00319b ↗
26. 10.1002/cmdc.20130026210.1002/cmdc.201300262 ↗
27. 10.1021/acs.chemrev.5b0026310.1021/acs.chemrev.5b00263 ↗
28. 10.1021/acsami.6b1137310.1021/acsami.6b11373 ↗
29. 10.1021/ja400337p10.1021/ja400337p ↗
30. 10.1021/acsami.5b1102310.1021/acsami.5b11023 ↗
31. 10.1021/ja403593910.1021/ja4035939 ↗
32. 10.1021/bc300249f10.1021/bc300249f ↗
33. 10.1039/c5sc03909f10.1039/c5sc03909f ↗
34. 10.1039/c4cc05999a10.1039/c4cc05999a ↗
35. 10.1039/c6nr02137a10.1039/c6nr02137a ↗
36. 10.1021/ja800892410.1021/ja8008924 ↗
37. 10.1021/ol901607g10.1021/ol901607g ↗
38. 10.1002/anie.20140690910.1002/anie.201406909 ↗
39. 10.1039/c5cc02389k10.1039/c5cc02389k ↗
40. 10.1002/anie.20100537510.1002/anie.201005375 ↗
41. 10.1039/b820397k10.1039/b820397k ↗
42. 10.1002/anie.20141054810.1002/anie.201410548 ↗
43. 10.1016/j.bmcl.2012.09.10910.1016/j.bmcl.2012.09.109 ↗
44. 10.1021/jo500604x10.1021/jo500604x ↗
45. 10.1021/ol403475v10.1021/ol403475v ↗
46. 10.1021/ja110401410.1021/ja1104014 ↗
47. 10.1021/acsami.6b0067510.1021/acsami.6b00675 ↗
48. 10.1016/j.dyepig.2011.10.00510.1016/j.dyepig.2011.10.005 ↗
49. 10.1021/jp020877f10.1021/jp020877f ↗
50. 10.1002/anie.20130813510.1002/anie.201308135 ↗
51. 10.1021/ja800570d10.1021/ja800570d ↗
52. 10.1038/nchem.12010.1038/nchem.120 ↗
53. 10.1021/ja511177e10.1021/ja511177e ↗
54. 10.1016/j.chembiol.2006.04.00710.1016/j.chembiol.2006.04.007 ↗
55. 10.1039/c7dt02273e10.1039/c7dt02273e ↗
56. 10.1038/212425a010.1038/212425a0 ↗
57. 10.1016/j.tox.2008.02.01810.1016/j.tox.2008.02.018 ↗
58. 10.1042/bj356054910.1042/bj3560549 ↗
59. 10.1002/jcb.2027710.1002/jcb.20277 ↗
60. 10.1016/j.freeradbiomed.2015.10.42510.1016/j.freeradbiomed.2015.10.425 ↗