Functionalized Metal–Organic Framework UiO-66-NH-BQB for Selective Detection of Hydrogen Sulfide and Cysteine
Source abstract
Abstract
Hydrogen sulfide (H2S) is an important signaling molecule related to many diseases. Thus, H2S has a great impact on the pathological and physiological processes in biological systems. Cysteine (l-Cys) is a building block for proteins and important metabolites. To understand their roles in the physiological metabolic procedures, the measurement of the H2S level and identifying cysteine in the biological system is significant. In this study, through the functionalization of UiO-66-NH2 by 4-(2,2-dicyanoethenyl)benzoic acid (BQB), a novel UiO-66-NH-BQB is successfully synthesized and used as a fluorescence probe to recognize and detect H2S and l-Cys. The fluorescence signals of the probe are enhanced great when it is exposed to H2S or cysteine molecules; thus, it is able to determine quantificationally the H2S concentration in an aqueous solution. The detection limitation of the UiO-66-NH-BQB to H2S concentration is found to be as low as 1.74 μM. The developed fluorescent probe based on UiO-66-NH-BQB displays a high selectivity and excellent biocompatibility, which is very promising for recognition and sensing of biothiols in organisms.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Sulfur Compounds in Biology · Metal-Organic Frameworks: Synthesis and Applications · Molecular Sensors and Ion Detection
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Shanghai Key Laboratory of Green Chemistry and Chemical Processes, Department of Chemistry, East China Normal University, Dongchuan Road 500, Shanghai 200241, China
Funding
Ministry of Education of the People's Republic of China · National Natural Science Foundation of China
References (52)
Show source-provided references
1. 10.1021/ja408909h10.1021/ja408909h ↗
2. 10.1146/annurev.neuro.26.041002.13104710.1146/annurev.neuro.26.041002.131047 ↗
3. 10.1523/jneurosci.16-03-01066.199610.1523/jneurosci.16-03-01066.1996 ↗
4. 10.1177/109158181038488210.1177/1091581810384882 ↗
5. 10.1021/ja303261d10.1021/ja303261d ↗
6. 10.1016/j.bbrc.2009.01.05910.1016/j.bbrc.2009.01.059 ↗
7. 10.1002/hep.2081710.1002/hep.20817 ↗
8. 10.1002/anie.20110423610.1002/anie.201104236 ↗
9. 10.1021/jacs.6b1253610.1021/jacs.6b12536 ↗
10. 10.1016/j.talanta.2010.10.04710.1016/j.talanta.2010.10.047 ↗
11. 10.1007/s10895-018-2269-510.1007/s10895-018-2269-5 ↗
12. 10.1038/s41598-018-38132-y10.1038/s41598-018-38132-y ↗
13. 10.1021/ac010541m10.1021/ac010541m ↗
14. 10.1016/j.nlm.2013.05.00610.1016/j.nlm.2013.05.006 ↗
15. 10.1038/srep0436610.1038/srep04366 ↗
16. 10.1016/j.snb.2019.01.14810.1016/j.snb.2019.01.148 ↗
17. 10.1039/c8dt04350g10.1039/c8dt04350g ↗
18. 10.1016/j.jssc.2017.07.02710.1016/j.jssc.2017.07.027 ↗
19. 10.1002/smll.20170382210.1002/smll.201703822 ↗
20. 10.1039/c2cc33909a10.1039/c2cc33909a ↗
21. 10.1039/b916476f10.1039/b916476f ↗
22. 10.1039/c6ce00032k10.1039/c6ce00032k ↗
23. 10.1002/adts.20180017010.1002/adts.201800170 ↗
24. 10.1002/anie.20190273810.1002/anie.201902738 ↗
25. 10.1039/c8nj06362a10.1039/c8nj06362a ↗
26. 10.1021/ja508360210.1021/ja5083602 ↗
27. 10.1002/anie.20180793510.1002/anie.201807935 ↗
28. 10.1016/j.seppur.2015.03.02010.1016/j.seppur.2015.03.020 ↗
29. 10.1016/j.micromeso.2018.08.00310.1016/j.micromeso.2018.08.003 ↗
30. 10.1021/acs.inorgchem.8b0236010.1021/acs.inorgchem.8b02360 ↗
31. 10.1016/j.ccr.2019.03.00510.1016/j.ccr.2019.03.005 ↗
32. 10.1016/j.ccr.2019.02.00110.1016/j.ccr.2019.02.001 ↗
33. 10.1166/jnn.2018.1537310.1166/jnn.2018.15373 ↗
34. 10.1016/j.cej.2017.03.00810.1016/j.cej.2017.03.008 ↗
35. 10.1039/c6tb03379b10.1039/c6tb03379b ↗
36. 10.1039/c8ta02794c10.1039/c8ta02794c ↗
37. 10.1002/smll.20170444010.1002/smll.201704440 ↗
38. 10.1039/c7nr08892b10.1039/c7nr08892b ↗
39. 10.1016/j.ccr.2019.02.03210.1016/j.ccr.2019.02.032 ↗
40. 10.1021/ja805795310.1021/ja8057953 ↗
41. 10.1021/jacs.6b1124010.1021/jacs.6b11240 ↗
42. 10.1039/c8cc01593g10.1039/c8cc01593g ↗
43. 10.1016/j.matlet.2018.12.12310.1016/j.matlet.2018.12.123 ↗
44. 10.1016/j.bios.2016.11.02110.1016/j.bios.2016.11.021 ↗
45. 10.1016/j.snb.2017.06.12010.1016/j.snb.2017.06.120 ↗
46. 10.1039/c0cc04092d10.1039/c0cc04092d ↗
47. 10.1002/adfm.20160598510.1002/adfm.201605985 ↗
48. 10.1039/c6cc02578a10.1039/c6cc02578a ↗
49. 10.1016/j.materresbull.2017.10.03810.1016/j.materresbull.2017.10.038 ↗
50. 10.1016/j.molcata.2015.06.01810.1016/j.molcata.2015.06.018 ↗
51. 10.1021/acsami.7b0909110.1021/acsami.7b09091 ↗
52. 10.1021/acs.inorgchem.6b0059810.1021/acs.inorgchem.6b00598 ↗