A highly selective AIE fluorogen for lipid droplet imaging in live cells and green algae
Source abstract
Abstract
Lipid droplets (LDs) are subcellular organelles for energy storage and lipid metabolism regulation. Here we report an aggregation-induced emission-active fluorogen, TPE-AmAl, for specific LD imaging. TPE-AmAl is cell-permeable: upon entering the live cells, the dye molecules can selectively accumulate in the LDs and turn on the fluorescence. TPE-AmAl possesses twisted intramolecular charge transfer properties as well: the emission colour in the hydrophobic LDs is blue-shifted by >100 nm than that in aqueous buffers. Compared with the commercial lipid droplet dye, TPE-AmAl demonstrates the advantages of low background, short staining time, high selectivity, excellent biocompatibility, and good photostability. The utilization of TPE-AmAl for LD staining in green algae is also demonstrated, indicating their potential application in the high-throughput screening of high-value microalgae as a preferential biofuel source.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Lipid metabolism and biosynthesis · Photosynthetic Processes and Mechanisms · Mass Spectrometry Techniques and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
HKUST-Shenzhen Research Institute
Shenzhen, China
Department of Chemistry
Division of Biomedical Engineering
Division of Life Science, State Key laboratory of Molecular Neuroscience, Institute of Molecular Functional Materials and Institute for Advanced Study
References (56)
Show source-provided references
1. Murphy · Prog. Lipid Res. · 2001 · 40 · 32510.1016/S0163-7827(01)00013-3 ↗
2. Zehmer · Proteomics · 2009 · 9 · 91410.1002/pmic.200800584 ↗
3. Kernohan · J. Dairy Res. · 1969 · 36 · 17710.1017/S002202990001267X ↗
4. Martin · Nat. Rev. Mol. Cell Biol. · 2006 · 7 · 37310.1038/nrm1912 ↗
5. Jiang · Proc. Natl. Acad. Sci. U. S. A. · 1992 · 89 · 785610.1073/pnas.89.17.7856 ↗
6. Wolins · J. Biol. Chem. · 2001 · 276 · 510110.1074/jbc.M006775200 ↗
7. Zhang · J. Proteome Res. · 2011 · 10 · 475710.1021/pr200553c ↗
8. Atheenstaedt · J. Bacteriol. · 1999 · 181 · 644110.1128/JB.181.20.6441-6448.1999 ↗
9. Blanchette-Mackie · J. Lipid Res. · 1995 · 36 · 121110.1016/S0022-2275(20)41129-0 ↗
10. Cohen · Diabetes · 2004 · 53 · 126110.2337/diabetes.53.5.1261 ↗
11. Bascom · Mol. Biol. Cell · 2003 · 14 · 93910.1091/mbc.E02-10-0633 ↗
12. Alberti · Lancet · 2005 · 366 · 105910.1016/S0140-6736(05)67402-8 ↗
13. Boulant · J. Gen. Virol. · 2007 · 88 · 220410.1099/vir.0.82898-0 ↗
14. Miyanari · Nat. Cell Biol. · 2007 · 9 · 108910.1038/ncb1631 ↗
15. Liang · Curr. Neurol. Neurosci. Rep. · 2011 · 11 · 9710.1007/s11910-010-0154-y ↗
16. Calore · Exp. Toxicol. Pathol. · 1999 · 51 · 2710.1016/S0940-2993(99)80054-2 ↗
17. Vermaak · Nat. Prod. Rep. · 2011 · 28 · 149310.1039/c1np00035g ↗
18. Davis · PLoS One · 2013 · 8 · e6763110.1371/journal.pone.0067631 ↗
19. Yonezawa · Mol. BioSyst. · 2011 · 7 · 9110.1039/C0MB00099J ↗
20. Chapman · Gut · 2002 · 51 · 910.1136/gut.51.1.9 ↗
21. Skelly · J. Hepatol. · 2001 · 35 · 19510.1016/S0168-8278(01)00094-0 ↗
22. Wijffels · Science · 2010 · 329 · 79610.1126/science.1189003 ↗
23. Ding · Nat. Protoc. · 2012 · 8 · 4310.1038/nprot.2012.142 ↗
24. Borisov · Chem. Rev. · 2008 · 108 · 42310.1021/cr068105t ↗
25. Greenspan · J. Cell Biol. · 1985 · 100 · 96510.1083/jcb.100.3.965 ↗
26. Jones · Nutr. Metab. · 2008 · 5 · 2310.1186/1743-7075-5-23 ↗
27. Spandl · Traffic · 2009 · 10 · 157910.1111/j.1600-0854.2009.00980.x ↗
28. Ohsaki · Histochem. Cell Biol. · 2010 · 133 · 47710.1007/s00418-010-0678-x ↗
29. Gocze · Cytometry · 1994 · 17 · 15110.1002/cyto.990170207 ↗
30. Loudet · Chem. Rev. · 2007 · 107 · 489110.1021/cr078381n ↗
31. O'Rourke · Cell Metab. · 2009 · 10 · 43010.1016/j.cmet.2009.10.002 ↗
32. Yen · PLoS One · 2010 · 5 · e1281010.1371/journal.pone.0012810 ↗
33. Förster · Z. Phys. Chem. · 1954 · 1 · 27510.1524/zpch.1954.1.5_6.275 ↗
34. Luo · Chem. Commun. · 2001 · 174010.1039/b105159h ↗
35. Dong · Chem. Commun. · 2007 · 325510.1039/b704794k ↗
36. Li · J. Phys. Chem. B · 2005 · 109 · 1006110.1021/jp0503462 ↗
37. Zeng · Chem. Commun. · 2007 · 7010.1039/B613522F ↗
38. Hong · Chem. Commun. · 2009 · 433210.1039/b904665h ↗
39. Liu · Chem. Rev. · 2009 · 109 · 579910.1021/cr900149d ↗
40. Hong · Chem. Soc. Rev. · 2011 · 40 · 536110.1039/c1cs15113d ↗
41. Zhao · J. Mater. Chem. · 2012 · 22 · 2372610.1039/c2jm31949g ↗
42. Leung · J. Am. Chem. Soc. · 2013 · 135 · 6210.1021/ja310324q ↗
43. Zhao · J. Mater. Chem. C · 2013 · 1 · 464010.1039/c3tc30759j ↗
44. Chen · J. Am. Chem. Soc. · 2013 · 135 · 492610.1021/ja400337p ↗
45. Wang · J. Am. Chem. Soc. · 2012 · 135 · 823810.1021/ja312581r ↗
46. Kim · Chem. Commun. · 2012 · 48 · 233110.1039/c2cc17496k ↗
47. Lee · Mol. BioSyst. · 2013 · 9 · 95210.1039/c2mb25479d ↗
48. Lee · Chem. Sci. · 2013 · 4 · 328210.1039/c3sc51344k ↗
49. Hong · J. Am. Chem. Soc. · 2012 · 134 · 168010.1021/ja208720a ↗
50. Chen · Chem. Sci. · 2012 · 3 · 180410.1039/c2sc01108e ↗
51. Rettlg · J. Phys. Chem. · 1982 · 86 · 197010.1021/j100208a013 ↗
52. Koenig · Chem. Sci. · 2013 · 4 · 250210.1039/c3sc50290b ↗
53. Grabowski · Chem. Rev. · 2003 · 103 · 389910.1021/cr940745l ↗
54. Fujimoto · Biol. Pharm. Bull. · 2006 · 29 · 217410.1248/bpb.29.2174 ↗
55. Zhao · J. Mater. Chem. · 2012 · 22 · 1512810.1039/c2jm31368e ↗
56. Hu · J. Mater. Chem. · 2012 · 22 · 23210.1039/C1JM13556B ↗