Independent Generation and Time‐Resolved Detection of 2′‐Deoxyguanosin‐N2‐yl Radicals. (2nd June 2020)
- Record Type:
- Journal Article
- Title:
- Independent Generation and Time‐Resolved Detection of 2′‐Deoxyguanosin‐N2‐yl Radicals. (2nd June 2020)
- Main Title:
- Independent Generation and Time‐Resolved Detection of 2′‐Deoxyguanosin‐N2‐yl Radicals
- Authors:
- Zheng, Liwei
Dai, Xiaojuan
Su, Hongmei
Greenberg, Marc M. - Abstract:
- Abstract: Guanine radicals are important reactive intermediates in DNA damage. Hydroxyl radical (HO . ) has long been believed to react with 2′‐deoxyguanosine (dG) generating 2′‐deoxyguanosin‐N1‐yl radical (dG(N1‐H) . ) via addition to the nucleobase π‐system and subsequent dehydration. This basic tenet was challenged by an alternative mechanism, in which the major reaction of HO . with dG was proposed to involve hydrogen atom abstraction from the N2‐amine. The 2′‐deoxyguanosin‐N2‐yl radical (dG(N2‐H) . ) formed was proposed to rapidly tautomerize to dG(N1‐H) . . We report the first independent generation of dG(N2‐H) . in high yield via photolysis of 1 . dG(N2‐H) . is directly observed upon nanosecond laser flash photolysis (LFP) of 1 . The absorption spectrum of dG(N2‐H) . is corroborated by DFT studies, and anti ‐ and syn ‐dG(N2‐H) . are resolved for the first time. The LFP experiments showed no evidence for tautomerization of dG(N2‐H) . to dG(N1‐H) . within hundreds of microseconds. This observation suggests that the generation of dG(N1‐H) . via dG(N2‐H) . following hydrogen atom abstraction from dG is unlikely to be a major pathway when HO . reacts with dG. Abstract : Guanine oxidation produces two major tautomeric 2′‐deoxyguanosin‐yl radicals—dG(N2‐H) . and dG(N1‐H) . . dG(N2‐H) . was independently generated from 1 . dG(N2‐H) . reacts significantly more slowly with thiol reducing agents than alkyl radicals. Contrary to previous reports, there is no evidence thatAbstract: Guanine radicals are important reactive intermediates in DNA damage. Hydroxyl radical (HO . ) has long been believed to react with 2′‐deoxyguanosine (dG) generating 2′‐deoxyguanosin‐N1‐yl radical (dG(N1‐H) . ) via addition to the nucleobase π‐system and subsequent dehydration. This basic tenet was challenged by an alternative mechanism, in which the major reaction of HO . with dG was proposed to involve hydrogen atom abstraction from the N2‐amine. The 2′‐deoxyguanosin‐N2‐yl radical (dG(N2‐H) . ) formed was proposed to rapidly tautomerize to dG(N1‐H) . . We report the first independent generation of dG(N2‐H) . in high yield via photolysis of 1 . dG(N2‐H) . is directly observed upon nanosecond laser flash photolysis (LFP) of 1 . The absorption spectrum of dG(N2‐H) . is corroborated by DFT studies, and anti ‐ and syn ‐dG(N2‐H) . are resolved for the first time. The LFP experiments showed no evidence for tautomerization of dG(N2‐H) . to dG(N1‐H) . within hundreds of microseconds. This observation suggests that the generation of dG(N1‐H) . via dG(N2‐H) . following hydrogen atom abstraction from dG is unlikely to be a major pathway when HO . reacts with dG. Abstract : Guanine oxidation produces two major tautomeric 2′‐deoxyguanosin‐yl radicals—dG(N2‐H) . and dG(N1‐H) . . dG(N2‐H) . was independently generated from 1 . dG(N2‐H) . reacts significantly more slowly with thiol reducing agents than alkyl radicals. Contrary to previous reports, there is no evidence that dG(N2‐H) . rearranges to dG(N1‐H) . on the sub‐millisecond timescale. … (more)
- Is Part Of:
- Angewandte Chemie. Volume 132:Number 32(2020)
- Journal:
- Angewandte Chemie
- Issue:
- Volume 132:Number 32(2020)
- Issue Display:
- Volume 132, Issue 32 (2020)
- Year:
- 2020
- Volume:
- 132
- Issue:
- 32
- Issue Sort Value:
- 2020-0132-0032-0000
- Page Start:
- 13508
- Page End:
- 13515
- Publication Date:
- 2020-06-02
- Subjects:
- DNA -- guanine oxidation -- laser flash photolysis -- oxidative stress -- radicals
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ange.202005300 ↗
- Languages:
- English
- ISSNs:
- 0044-8249
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0902.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24585.xml