Stepwise nitrosylation of the nonheme iron site in an engineered azurin and a molecular basis for nitric oxide signaling mediated by nonheme iron proteins. Issue 19 (16th April 2021)
- Record Type:
- Journal Article
- Title:
- Stepwise nitrosylation of the nonheme iron site in an engineered azurin and a molecular basis for nitric oxide signaling mediated by nonheme iron proteins. Issue 19 (16th April 2021)
- Main Title:
- Stepwise nitrosylation of the nonheme iron site in an engineered azurin and a molecular basis for nitric oxide signaling mediated by nonheme iron proteins
- Authors:
- Tian, Shiliang
Fan, Ruixi
Albert, Therese
Khade, Rahul L.
Dai, Huiguang
Harnden, Kevin A.
Hosseinzadeh, Parisa
Liu, Jing
Nilges, Mark J.
Zhang, Yong
Moënne-Loccoz, Pierre
Guo, Yisong
Lu, Yi - Abstract:
- Abstract : Stepwise nitrosylation from Fe(ii ) to {FeNO} 7, {FeNO} 8 and then to {Fe(NO)2 } 9 is reported for the first time in the same protein scaffold, providing deeper understanding of the detailed mechanism of dinitrosyl iron complex formation. Abstract : Mononitrosyl and dinitrosyl iron species, such as {FeNO} 7, {FeNO} 8 and {Fe(NO)2 } 9, have been proposed to play pivotal roles in the nitrosylation processes of nonheme iron centers in biological systems. Despite their importance, it has been difficult to capture and characterize them in the same scaffold of either native enzymes or their synthetic analogs due to the distinct structural requirements of the three species, using redox reagents compatible with biomolecules under physiological conditions. Here, we report the realization of stepwise nitrosylation of a mononuclear nonheme iron site in an engineered azurin under such conditions. Through tuning the number of nitric oxide equivalents and reaction time, controlled formation of {FeNO} 7 and {Fe(NO)2 } 9 species was achieved, and the elusive {FeNO} 8 species was inferred by EPR spectroscopy and observed by Mössbauer spectroscopy, with complemental evidence for the conversion of {FeNO} 7 to {Fe(NO)2 } 9 species by UV-Vis, resonance Raman and FT-IR spectroscopies. The entire pathway of the nitrosylation process, Fe(ii ) → {FeNO} 7 → {FeNO} 8 → {Fe(NO)2 } 9, has been elucidated within the same protein scaffold based on spectroscopic characterization and DFTAbstract : Stepwise nitrosylation from Fe(ii ) to {FeNO} 7, {FeNO} 8 and then to {Fe(NO)2 } 9 is reported for the first time in the same protein scaffold, providing deeper understanding of the detailed mechanism of dinitrosyl iron complex formation. Abstract : Mononitrosyl and dinitrosyl iron species, such as {FeNO} 7, {FeNO} 8 and {Fe(NO)2 } 9, have been proposed to play pivotal roles in the nitrosylation processes of nonheme iron centers in biological systems. Despite their importance, it has been difficult to capture and characterize them in the same scaffold of either native enzymes or their synthetic analogs due to the distinct structural requirements of the three species, using redox reagents compatible with biomolecules under physiological conditions. Here, we report the realization of stepwise nitrosylation of a mononuclear nonheme iron site in an engineered azurin under such conditions. Through tuning the number of nitric oxide equivalents and reaction time, controlled formation of {FeNO} 7 and {Fe(NO)2 } 9 species was achieved, and the elusive {FeNO} 8 species was inferred by EPR spectroscopy and observed by Mössbauer spectroscopy, with complemental evidence for the conversion of {FeNO} 7 to {Fe(NO)2 } 9 species by UV-Vis, resonance Raman and FT-IR spectroscopies. The entire pathway of the nitrosylation process, Fe(ii ) → {FeNO} 7 → {FeNO} 8 → {Fe(NO)2 } 9, has been elucidated within the same protein scaffold based on spectroscopic characterization and DFT calculations. These results not only enhance the understanding of the dinitrosyl iron complex formation process, but also shed light on the physiological roles of nitric oxide signaling mediated by nonheme iron proteins. … (more)
- Is Part Of:
- Chemical science. Volume 12:Issue 19(2021)
- Journal:
- Chemical science
- Issue:
- Volume 12:Issue 19(2021)
- Issue Display:
- Volume 12, Issue 19 (2021)
- Year:
- 2021
- Volume:
- 12
- Issue:
- 19
- Issue Sort Value:
- 2021-0012-0019-0000
- Page Start:
- 6569
- Page End:
- 6579
- Publication Date:
- 2021-04-16
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1sc00364j ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 17289.xml