Photoinduced electron transfer reaction in mitochondria for spatiotemporal selective photo-oxidation of lipids by donor/acceptor linked molecules
Source abstract
Abstract
Donor-acceptor-linked molecules have been synthesized and utilized to induce the rapid and site-selective lipid-oxidation in mitochondria by utilizing a photoinduced intermolecular electron transfer reaction. Two water-soluble donor-acceptor molecules (1 and 2) were designed and synthesized for this purpose. 2 was prepared to modulate its affinity to cell membrane in mitochondria. Confocal laser microscopy experiments revealed that 1 and 2 possess high localization abilities in mitochondria. By the photoinduced electron transfer, 2 exhibited the remarkable oxidation ability of lipids, mainly cardiolipin. In HeLa cells, 2 triggered mitochondrial lipid oxidation, which was followed by apoptotic cell death, under illumination within a few seconds. These results show that the present molecular system is highly promising to utilize the photoinduced intermolecular electron transfer reaction in a precise spatiotemporal manner in a cell by using light.
Source: openalex_inverted_index · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Photochromic and Fluorescence Chemistry · Photoreceptor and optogenetics research · Porphyrin and Phthalocyanine Chemistry
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Integrated Cell-Material Sciences (WPI-iCeMS)
Kyoto University
Kyoto 606-8501
Japan
Research Institute for Electronic Science
Department of Molecular Engineering
Graduate School of Engineering
Kyoto 615-8510
Funding
Japan Society for the Promotion of Science
References (26)
Show source-provided references
1. Brieke · Angew. Chem., Int. Ed. · 2012 · 51 · 844610.1002/anie.201202134 ↗
2. Schweitzer · Chem. Rev. · 2003 · 103 · 168510.1021/cr010371d ↗
3. Spiller · Nature · 2010 · 465 · 73610.1038/nature09232 ↗
4. Numata · J. Am. Chem. Soc. · 2012 · 134 · 609210.1021/ja3007275 ↗
5. Takano · Chem. Sci. · 2016 · 7 · 333110.1039/C5SC04135J ↗
6. Santos · Antioxid. Redox Signaling · 2009 · 11 · 240910.1089/ars.2009.2625 ↗
7. Takagi · J. Cereb. Blood Flow Metab. · 1998 · 18 · 20610.1097/00004647-199802000-00012 ↗
8. Igamberdiev · Physiol. Plant. · 2001 · 111 · 42710.1034/j.1399-3054.2001.1110402.x ↗
9. Willie · Biochemistry · 1992 · 31 · 723710.1021/bi00147a005 ↗
10. Wang · Genes Dev. · 2001 · 15 · 2922
11. Mao · ACS Chem. Biol. · 2016 · 11 · 53010.1021/acschembio.5b00737 ↗
12. Schlame · Prog. Lipid Res. · 2000 · 39 · 25710.1016/S0163-7827(00)00005-9 ↗
13. Pfeiffer · J. Biol. Chem. · 2003 · 278 · 5287310.1074/jbc.M308366200 ↗
14. Orrenius · Nat. Chem. Biol. · 2005 · 1 · 18810.1038/nchembio0905-188 ↗
15. Yin · Free Radical Res. · 2012 · 46 · 95910.3109/10715762.2012.676642 ↗
16. Fukuzumi · J. Am. Chem. Soc. · 2004 · 126 · 160010.1021/ja038656q ↗
17. Erbrich · Histochemistry · 1982 · 74 · 110.1007/BF00495046 ↗
18. Kobayashi · Angew. Chem., Int. Ed. · 2016 · 55 · 1401910.1002/anie.201607419 ↗
19. Chae · ACS Nano · 2010 · 4 · 501110.1021/nn100620d ↗
20. Tyurina · Mol. Pharmacol. · 2006 · 70 · 70610.1124/mol.106.022731 ↗
21. Tsudaka · Chem. – Eur. J. · 2017 · 23 · 130610.1002/chem.201604527 ↗
22. Fukuzumi · J. Am. Chem. Soc. · 2010 · 132 · 1100210.1021/ja105314x ↗
23. Fukuzumi · Phys. Chem. Chem. Phys. · 2008 · 10 · 515910.1039/b809264h ↗
24. Laguerre · Prog. Lipid Res. · 2007 · 46 · 24410.1016/j.plipres.2007.05.002 ↗
25. Shioji · Bioorg. Med. Chem. Lett. · 2010 · 20 · 391110.1016/j.bmcl.2010.05.017 ↗
26. Manders · J. Microsc. · 1993 · 169 · 37510.1111/j.1365-2818.1993.tb03313.x ↗