Interaction of nitrite with ferric protoglobin from Methanosarcina acetivorans – an interesting model for spectroscopic studies of the haem–ligand interaction. Issue 10 (18th January 2023)
- Record Type:
- Journal Article
- Title:
- Interaction of nitrite with ferric protoglobin from Methanosarcina acetivorans – an interesting model for spectroscopic studies of the haem–ligand interaction. Issue 10 (18th January 2023)
- Main Title:
- Interaction of nitrite with ferric protoglobin from Methanosarcina acetivorans – an interesting model for spectroscopic studies of the haem–ligand interaction
- Authors:
- Sgammato, Roberta
Van Brempt, Niels
Aerts, Roy
Van Doorslaer, Sabine
Dewilde, Sylvia
Herrebout, Wouter
Johannessen, Christian - Abstract:
- Abstract : Advanced spectroscopic analysis shows that ferric M. acetivorans protoglobin selectively binds nitric oxide under nitrite-rich conditions in which many ferric globins show nitrite coordination and haem greening, highlighting its resilience to RNS. Abstract : Protoglobin from Methanosarcina acetivorans ( Ma Pgb) is a dimeric globin belonging to the same lineage of the globin superfamily as globin-coupled sensors. A putative role in the scavenging of reactive nitrogen and oxygen species has been suggested as a possible adaptation mechanism of the host organism to different gaseous environments in the course of evolution. A combination of optical absorption, electronic circular dichroism (ECD), resonance Raman (rRaman), and electron paramagnetic resonance (EPR) reveal the unusual in vitro reaction of ferric Ma Pgb with nitrite. In contrast to other globins, a large excess of nitrite did not induce the formation of a nitriglobin form in Ma Pgb. Surprisingly, the addition of nitrite in mildly acidic pH led to the formation of a stable nitric-oxide ligated ferric form of the protein ( Ma Pgb–NO). Furthermore, the 300–700 nm ECD spectrum of ferric Ma Pgb is for the first time reported and discussed, showing strong differences in the Soret and Q ellipticity compared to ferric myoglobin, in line with the unusually strongly ruffled haem group of Ma Pgb and the related quantum-mechanical admixture of the S = 5/2 and S = 3/2 state of its ferric form. The Soret and QAbstract : Advanced spectroscopic analysis shows that ferric M. acetivorans protoglobin selectively binds nitric oxide under nitrite-rich conditions in which many ferric globins show nitrite coordination and haem greening, highlighting its resilience to RNS. Abstract : Protoglobin from Methanosarcina acetivorans ( Ma Pgb) is a dimeric globin belonging to the same lineage of the globin superfamily as globin-coupled sensors. A putative role in the scavenging of reactive nitrogen and oxygen species has been suggested as a possible adaptation mechanism of the host organism to different gaseous environments in the course of evolution. A combination of optical absorption, electronic circular dichroism (ECD), resonance Raman (rRaman), and electron paramagnetic resonance (EPR) reveal the unusual in vitro reaction of ferric Ma Pgb with nitrite. In contrast to other globins, a large excess of nitrite did not induce the formation of a nitriglobin form in Ma Pgb. Surprisingly, the addition of nitrite in mildly acidic pH led to the formation of a stable nitric-oxide ligated ferric form of the protein ( Ma Pgb–NO). Furthermore, the 300–700 nm ECD spectrum of ferric Ma Pgb is for the first time reported and discussed, showing strong differences in the Soret and Q ellipticity compared to ferric myoglobin, in line with the unusually strongly ruffled haem group of Ma Pgb and the related quantum-mechanical admixture of the S = 5/2 and S = 3/2 state of its ferric form. The Soret and Q ellipticity change strongly upon formation of Ma Pgb–NO, revealing a significant effect of the nitric-oxide ligation on the haem group and pocket. The related changes in the asymmetric pyrrole half-ring stretching vibration modes observed in the rRaman spectra give experimental support to earlier theoretical models, in which an important role of the in-plane breathing modes of the haem was predicted for the stabilization of the binding of diatomic gases to Ma Pgb. … (more)
- Is Part Of:
- Dalton transactions. Volume 52:Issue 10(2023)
- Journal:
- Dalton transactions
- Issue:
- Volume 52:Issue 10(2023)
- Issue Display:
- Volume 52, Issue 10 (2023)
- Year:
- 2023
- Volume:
- 52
- Issue:
- 10
- Issue Sort Value:
- 2023-0052-0010-0000
- Page Start:
- 2976
- Page End:
- 2987
- Publication Date:
- 2023-01-18
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2dt03252j ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26120.xml