journal article·2019

Visual detection of odorant geraniol enabled by integration of a human olfactory receptor into polydiacetylene/lipid nano-assembly

Taegon Kim, Dongseok Moon, Jin Hyuk Park, Heehong Yang, Seongyeon Cho, Tai Hyun Park, Dong June Ahn

Nanoscale· Volume 11· Issue 16
Publisher page

Abstract

A new polydiacetylene lipid/human olfactory receptor nano-assembly was fabricated for the visual detection of an odorant for the first time. The assembly consisted of phospholipid-mixed polydiacetylenes (PDAs) and human olfactory receptors (hORs) in detergent micelles. To overcome the limitations of bioelectronic noses, hOR-embedded chromatic complexes (PDA/hORs) were developed, introducing PDAs that showed color and fluorescence transitions against various stimuli. The chromatic nanocomplexes reacted with target molecules, showing a fluorescence intensity increase in a dose-dependent manner and target selectivity among various odorants. As a result, a color transition of the assembly from blue to purple occurred, allowing the visual detection of the odorant geraniol. Through circular dichroism (CD) spectroscopy and a tryptophan fluorescence quenching method, the structural and functional properties of the hORs embedded in the complexes were confirmed. Based on this first work, future array devices, integrating multiple nano-assemblies, can be substantiated and utilized in environmental assessment and analysis of food quality.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Polydiacetylene-based materials and applications · Supramolecular Self-Assembly in Materials · Advanced Chemical Sensor Technologies

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

Affiliations

Department of Chemical and Biological Engineering

Korea University

Seoul 02841

Korea

School of Chemical and Biological Engineering

Institute of Chemical Processes, Seoul National University

Seoul 08826

Republic of Korea

KU-KIST School of Converging Science and Technology

Funding

National Research Foundation of Korea · Korea University

References (44)

Show source-provided references
1. Bockaert · EMBO J. · 1999 · 18 · 172310.1093/emboj/18.7.1723 ↗
2. Firestein · Nature · 2001 · 413 · 21110.1038/35093026 ↗
3. Yoon · Angew. Chem., Int. Ed. · 2009 · 48 · 275510.1002/anie.200805171 ↗
4. Kim · Adv. Mater. · 2009 · 21 · 9110.1002/adma.200801435 ↗
5. Jin · Biosens. Bioelectron. · 2012 · 35 · 33510.1016/j.bios.2012.03.012 ↗
6. Yang · Biotechnol. Bioprocess Eng. · 2015 · 20 · 42310.1007/s12257-014-0897-4 ↗
7. Lim · Adv. Healthcare Mater. · 2014 · 3 · 36010.1002/adhm.201300174 ↗
8. Lim · Biosens. Bioelectron. · 2013 · 39 · 24410.1016/j.bios.2012.07.054 ↗
9. Ahn · Sens. Actuators, B · 2015 · 210 · 910.1016/j.snb.2014.12.060 ↗
10. Lee · Biosens. Bioelectron. · 2015 · 71 · 17910.1016/j.bios.2015.04.033 ↗
11. Son · Biotechnol. Bioprocess Eng. · 2017 · 87 · 901
12. Son · Biosens. Bioelectron. · 2015 · 74 · 19910.1016/j.bios.2015.06.053 ↗
13. Daniel · Chem. Rev. · 2004 · 104 · 29310.1021/cr030698+ ↗
14. Miyata · Chem. Soc. Rev. · 2012 · 41 · 256210.1039/C1CS15258K ↗
15. Hasegawa · Chem. Commun. · 2004 · 2004 · 215010.1039/b407409b ↗
16. Kim · Adv. Mater. · 2004 · 16 · 175310.1002/adma.200306664 ↗
17. Jiang · Acc. Chem. Res. · 2018 · 51 · 184010.1021/acs.accounts.8b00242 ↗
18. Miao · Angew. Chem., Int. Ed. · 2018 · 57 · 125610.1002/anie.201710727 ↗
19. Kuwana · Cell · 2002 · 111 · 33110.1016/S0092-8674(02)01036-X ↗
20. Aida · Science · 2012 · 335 · 81310.1126/science.1205962 ↗
21. Lkkala · Science · 2002 · 29 · 2407
22. Plant · Langmuir · 1999 · 15 · 512810.1021/la981662t ↗
23. Otero · Electrochim. Acta · 2012 · 84 · 11210.1016/j.electacta.2012.03.097 ↗
24. Charych · Science · 1993 · 261 · 58510.1126/science.8342021 ↗
25. Berman · Science · 1995 · 269 · 51510.1126/science.269.5223.515 ↗
26. Okada · Acc. Chem. Res. · 1998 · 31 · 22910.1021/ar970063v ↗
27. Ji · Bull. Korean Chem. Soc. · 2002 · 24 · 667
28. Cho · Chem. Lett. · 2003 · 32 · 28210.1246/cl.2003.282 ↗
29. Kim · Macromolecules · 2005 · 38 · 936610.1021/ma051551i ↗
30. Ahn · Acc. Chem. Res. · 2008 · 41 · 80510.1021/ar7002489 ↗
31. Ahn · Adv. Funct. Mater. · 2009 · 19 · 148310.1002/adfm.200801074 ↗
32. Kolusheva · J. Lipid Res. · 2003 · 44 · 6510.1194/jlr.M200136-JLR200 ↗
33. Porat · Biochemistry · 2003 · 42 · 1097110.1021/bi034889i ↗
34. Kolusheva · J. Am. Chem. Soc. · 2005 · 127 · 1000010.1021/ja052436q ↗
35. Friedman · Anal. Chem. · 2008 · 80 · 780410.1021/ac801254v ↗
36. Subramaniam · Langmuir · 2008 · 24 · 1106710.1021/la801835g ↗
37. Akbar · J. Bioenerg. Biomembr. · 2016 · 48 · 24110.1007/s10863-016-9653-0 ↗
38. Vaiana · J. Am. Chem. Soc. · 2003 · 125 · 1456410.1021/ja036082j ↗
39. Marmé · Angew. Chem., Int. Ed. · 2004 · 43 · 379810.1002/anie.200453835 ↗
40. de March · Flavour Fragrance J. · 2015 · 30 · 34210.1002/ffj.3249 ↗
41. Yang · ACS Nano · 2017 · 11 · 1184710.1021/acsnano.7b04992 ↗
42. Chance · J. Chem. Phys. · 1979 · 71 · 20610.1063/1.438117 ↗
43. Kolusheva · Biochemistry · 2000 · 39 · 1585110.1021/bi000570b ↗
44. Helfrich · Phys. Lett. · 1974 · 50 · 11510.1016/0375-9601(74)90899-8 ↗