Ability of the Putative Decomposition Products of 2, 3‐dioxetanes of Indoles to Photosensitize Cyclobutane Pyrimidine Dimer (CPD) Formation and its Implications for the "Dark" (Chemisensitized) Pathway to CPDs in Melanocytes†. (11th October 2021)
- Record Type:
- Journal Article
- Title:
- Ability of the Putative Decomposition Products of 2, 3‐dioxetanes of Indoles to Photosensitize Cyclobutane Pyrimidine Dimer (CPD) Formation and its Implications for the "Dark" (Chemisensitized) Pathway to CPDs in Melanocytes†. (11th October 2021)
- Main Title:
- Ability of the Putative Decomposition Products of 2, 3‐dioxetanes of Indoles to Photosensitize Cyclobutane Pyrimidine Dimer (CPD) Formation and its Implications for the "Dark" (Chemisensitized) Pathway to CPDs in Melanocytes†
- Authors:
- Wang, Yanjing
Cacchillo, Elena M.
Niedzwiedzki, Dariusz M.
Taylor, John‐Stephen - Abstract:
- Abstract: The formation of cyclobutane pyrimidine dimers (CPDs) by a "dark" pathway in melanocytes has been attributed to chemisensitization by dioxetanes produced from peroxynitrite oxidation of melanin or melanin precursors. These dioxetanes are proposed to decompose to triplet state compounds which sensitize CPD formation by triplet–triplet energy transfer. To determine whether such compounds are capable of sensitizing CPD formation, the putative decomposition products of 2, 3‐dioxetanes of variously substituted indoles were synthesized and their triplet state energies determined at 77 K. Their ability to photosensitize CPD formation was determined by an enzyme‐coupled gel electrophoresis assay in comparison with norfloxacin (NFX) which has the lowest triplet energy known to sensitize CPD formation. The decomposition products of 2, 3‐dioxetanes of 5‐hydroxy and 5, 6‐dimethoxy indoles used as models for melanin precursors had lower triplet energies and were incapable of photosensitizing CPD formation. Theoretical calculations suggest that the decomposition products of the 2, 3‐dioxetanes of melanin precursors DHI and DHICA will have similarly low triplet energies. Decomposition products of the 2, 3‐dioxetanes of indoles lacking oxygen substituents had higher triplet energies than NFX and were capable of photosensitizing CPD formation, suggesting that peroxynitrite oxidation of tryptophan could play a hitherto unrecognized role in the dark pathway to CPDs. Abstract :Abstract: The formation of cyclobutane pyrimidine dimers (CPDs) by a "dark" pathway in melanocytes has been attributed to chemisensitization by dioxetanes produced from peroxynitrite oxidation of melanin or melanin precursors. These dioxetanes are proposed to decompose to triplet state compounds which sensitize CPD formation by triplet–triplet energy transfer. To determine whether such compounds are capable of sensitizing CPD formation, the putative decomposition products of 2, 3‐dioxetanes of variously substituted indoles were synthesized and their triplet state energies determined at 77 K. Their ability to photosensitize CPD formation was determined by an enzyme‐coupled gel electrophoresis assay in comparison with norfloxacin (NFX) which has the lowest triplet energy known to sensitize CPD formation. The decomposition products of 2, 3‐dioxetanes of 5‐hydroxy and 5, 6‐dimethoxy indoles used as models for melanin precursors had lower triplet energies and were incapable of photosensitizing CPD formation. Theoretical calculations suggest that the decomposition products of the 2, 3‐dioxetanes of melanin precursors DHI and DHICA will have similarly low triplet energies. Decomposition products of the 2, 3‐dioxetanes of indoles lacking oxygen substituents had higher triplet energies than NFX and were capable of photosensitizing CPD formation, suggesting that peroxynitrite oxidation of tryptophan could play a hitherto unrecognized role in the dark pathway to CPDs. Abstract : Decomposition products of oxygen‐substituted 2, 3‐dioxetanes of indoles related to melanin implicated in the dark pathway to CPDs were found to have triplet states below the threshold for sensitizing CPD formation and were unable to photosensitize CPD formation. In contrast, unsubstituted products related to tryptophan had higher triplet energies and were able to photosensitize CPD formation, suggesting a role for tryptophan in the dark pathway. … (more)
- Is Part Of:
- Photochemistry and photobiology. Volume 98:Number 2(2022)
- Journal:
- Photochemistry and photobiology
- Issue:
- Volume 98:Number 2(2022)
- Issue Display:
- Volume 98, Issue 2 (2022)
- Year:
- 2022
- Volume:
- 98
- Issue:
- 2
- Issue Sort Value:
- 2022-0098-0002-0000
- Page Start:
- 442
- Page End:
- 454
- Publication Date:
- 2021-10-11
- Subjects:
- Photochemistry -- Periodicals
Light -- Physiological effect -- Periodicals
541.35 - Journal URLs:
- http://www.blackwellpublishing.com/journal.asp?ref=0031-8655&site=1 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/php.13529 ↗
- Languages:
- English
- ISSNs:
- 0031-8655
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6465.985000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 20765.xml