A Unique Type of Pyrrole-Based Cyanine Fluorophores with Turn-on and Ratiometric Fluorescence Signals at Different pH Regions for Sensing pH in Enzymes and Living Cells
Source abstract
Abstract
The development of new functional fluorescent dyes has attracted great attention. Herein we have described a novel strategy to design a unique type of cyanine dyes by attaching two indolium moieties at the α-positions of the pyrrole core. The new type of cyanine dyes is named as PyCy fluorophores. Importantly, PyCy dyes can exhibit an exceptional feature, fluorescence turn-on response at pH varying from acidic to near-neutral conditions, and a ratiometric fluorescence response at pH varying from near-neutral to basic conditions. By taking advantage of the fluorescence turn-on response of PyCy2 at pH varying from acidic to near-neutral conditions and emission properties of PyCy2, we have demonstrated that a small-molecule fluorescent probe can image pH variations in living cells. Furthermore, we have demonstrated that PyCy2 can sense real-time pH changes under alkaline conditions induced by enzymes based on the ratiometric fluorescence response of PyCy2 at pH varying from near-neutral to basic conditions. We expect that the new design strategy for PyCy fluorophores may prompt the development of a wide variety of cyanine derivatives with desirable properties.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Molecular Sensors and Ion Detection · Luminescence and Fluorescent Materials · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, Hunan 410082, P. R. China
Institute of Fluorescent Probes for Biological Imaging, School of Chemistry and Chemical Engineering, School of Biological Science and Technology, University of Jinan, Jinan, Shandong 250022, P. R. China
Funding
National Natural Science Foundation of China · University of Jinan
References (36)
Show source-provided references
1. Boens N. · Chem. Soc. Rev. · 2012 · 41 · 113010.1039/C1CS15132K ↗
2. Wood T. E. · Chem. Rev. · 2007 · 107 · 183110.1021/cr050052c ↗
3. Zhang X. · ACS Appl. Mater. Interfaces · 2014 · 6 · 1237210.1021/am503849c ↗
4. Glayden, J.; Greeves, N.; Warren, S.; Wother, P.Organic Chemistry;Oxford University Press:Cary, NC, 2000; p203and p 1164.
5. CAS registry numbers 5919-26-6 and 114536-31-1 fromhttps://scifinder.cas.org/scifinder/view/scifinder/scifinderExplore.jsf.
6. Chen S. · J. Am. Chem. Soc. · 2013 · 135 · 492610.1021/ja400337p ↗
7. Chen Y. · Angew. Chem., Int. Ed. · 2013 · 52 · 168810.1002/anie.201207701 ↗
8. Huang X. · Chem. Commun. · 2012 · 48 · 1219510.1039/c2cc37094h ↗
9. Zheng H. · Chem. Commun. · 2012 · 48 · 224310.1039/c2cc17388c ↗
10. Feng X. J. · Org. Lett. · 2010 · 12 · 219410.1021/ol100474b ↗
11. Yang L. · ACS Appl. Mater. Interfaces · 2013 · 5 · 131710.1021/am303152w ↗
12. Varadi A. · Endocrinology · 2004 · 145 · 454010.1210/en.2004-0241 ↗
13. Ohkuma S. · Proc. Natl. Acad. Sci. U. S. A. · 1978 · 75 · 332710.1073/pnas.75.7.3327 ↗
14. Ishaque A. · J. Immunol. Methods · 1998 · 221 · 4310.1016/S0022-1759(98)00166-5 ↗
15. Pérez-Sala D. · J. Biol. Chem. · 1995 · 270 · 623510.1074/jbc.270.11.6235 ↗
16. Gardner A. · Curr. Psychiatry Rev. · 2005 · 1 · 25510.2174/157340005774575064 ↗
17. Lesnefsky E. J. · J. Mol. Cell Cardiol. · 2001 · 33 · 106510.1006/jmcc.2001.1378 ↗
18. Krulwich T. A. · Annu. Rev. Microbiol. · 1989 · 43 · 43510.1146/annurev.mi.43.100189.002251 ↗
19. Ito S. · Extremophiles · 1997 · 1 · 6110.1007/s007920050015 ↗
20. Yang Y. · Chem. Rev. · 2013 · 113 · 19210.1021/cr2004103 ↗
21. Cheng X. · ACS Appl. Mater. Interfaces · 2012 · 4 · 438710.1021/am3010412 ↗
22. Lu X. · ACS Appl. Mater. Interfaces · 2012 · 4 · 365710.1021/am300751p ↗
23. Han J. · Chem. Rev. · 2010 · 110 · 270910.1021/cr900249z ↗
24. Peng X. · J. Am. Chem. Soc. · 2005 · 127 · 417010.1021/ja043413z ↗
25. Tang B. · J. Am. Chem. Soc. · 2009 · 131 · 301610.1021/ja809149g ↗
26. Ke G. · ACS Appl. Mater. Interfaces · 2014 · 6 · 1532910.1021/am503818n ↗
27. Knizhnikov V. A. · Russ. J. Org. Chem. · 2007 · 43 · 85510.1134/S1070428007060097 ↗
28. Zimmermann T. · J. Heterocycl. Chem. · 2004 · 41 · 10310.1002/jhet.5570410117 ↗
29. Magde D. · Photochem. Photobiol. · 1999 · 70 · 73710.1111/j.1751-1097.1999.tb08277.x ↗
30. Oushiki D. · J. Am. Chem. Soc. · 2010 · 132 · 279510.1021/ja910090v ↗
31. Whitaker J. E. · Anal. Biochem. · 1991 · 194 · 33010.1016/0003-2697(91)90237-N ↗
32. Hoye A. T. · Acc. Chem. Res. · 2008 · 41 · 8710.1021/ar700135m ↗
33. Soltoff S. P. · J. Membr. Biol. · 1986 · 94 · 15310.1007/BF01871195 ↗
34. Vijayvergiya C. · Biochemistry · 2004 · 43 · 1529610.1021/bi048745v ↗
35. Catrina I. · J. Am. Chem. Soc. · 2007 · 129 · 576010.1021/ja069111+ ↗
36. Jia L. · Chem. Commun. · 2010 · 46 · 716610.1039/c0cc01244k ↗