Redox manipulation of the manganese metal in human manganese superoxide dismutase for neutron diffraction. Issue 10 (3rd October 2018)
- Record Type:
- Journal Article
- Title:
- Redox manipulation of the manganese metal in human manganese superoxide dismutase for neutron diffraction. Issue 10 (3rd October 2018)
- Main Title:
- Redox manipulation of the manganese metal in human manganese superoxide dismutase for neutron diffraction
- Authors:
- Azadmanesh, Jahaun
Lutz, William E.
Weiss, Kevin L.
Coates, Leighton
Borgstahl, Gloria E. O. - Abstract:
- Abstract : Human mitochondrial manganese superoxide dismutase (MnSOD) is a major player in combating reactive oxygen species in the human body. Methods have been found to control the redox state of the active‐site metal of large perdeuterated MnSOD crystals. Neutron diffraction data from these crystals were collected to study the effect of the redox state on proton location. These methods can be applied to other crystal systems where information on the location of protons in specific chemical states is needed. Abstract : Human manganese superoxide dismutase (MnSOD) is one of the most significant enzymes in preventing mitochondrial dysfunction and related diseases by combating reactive oxygen species (ROS) in the mitochondrial matrix. Mitochondria are the source of up to 90% of cellular ROS generation, and MnSOD performs its necessary bioprotective role by converting superoxide into oxygen and hydrogen peroxide. This vital catalytic function is conducted via cyclic redox reactions between the substrate and the active‐site manganese using proton‐coupled electron transfers. Owing to protons being difficult to detect experimentally, the series of proton transfers that compose the catalytic mechanism of MnSOD are unknown. Here, methods are described to discern the proton‐based mechanism using chemical treatments to control the redox state of large perdeuterated MnSOD crystals and subsequent neutron diffraction. These methods could be applicable to other crystal systems in whichAbstract : Human mitochondrial manganese superoxide dismutase (MnSOD) is a major player in combating reactive oxygen species in the human body. Methods have been found to control the redox state of the active‐site metal of large perdeuterated MnSOD crystals. Neutron diffraction data from these crystals were collected to study the effect of the redox state on proton location. These methods can be applied to other crystal systems where information on the location of protons in specific chemical states is needed. Abstract : Human manganese superoxide dismutase (MnSOD) is one of the most significant enzymes in preventing mitochondrial dysfunction and related diseases by combating reactive oxygen species (ROS) in the mitochondrial matrix. Mitochondria are the source of up to 90% of cellular ROS generation, and MnSOD performs its necessary bioprotective role by converting superoxide into oxygen and hydrogen peroxide. This vital catalytic function is conducted via cyclic redox reactions between the substrate and the active‐site manganese using proton‐coupled electron transfers. Owing to protons being difficult to detect experimentally, the series of proton transfers that compose the catalytic mechanism of MnSOD are unknown. Here, methods are described to discern the proton‐based mechanism using chemical treatments to control the redox state of large perdeuterated MnSOD crystals and subsequent neutron diffraction. These methods could be applicable to other crystal systems in which proton information on the molecule in question in specific chemical states is desired. … (more)
- Is Part Of:
- Acta crystallographica. Volume 74:Issue 10(2018:Oct.)
- Journal:
- Acta crystallographica
- Issue:
- Volume 74:Issue 10(2018:Oct.)
- Issue Display:
- Volume 74, Issue 10 (2018)
- Year:
- 2018
- Volume:
- 74
- Issue:
- 10
- Issue Sort Value:
- 2018-0074-0010-0000
- Page Start:
- 677
- Page End:
- 687
- Publication Date:
- 2018-10-03
- Subjects:
- manganese superoxide dismutase -- neutron diffraction -- perdeuteration -- human -- oxidation -- reduction -- large unit cell
Crystallography -- Periodicals
Crystals -- Periodicals
548 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)2053-230X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1107/S2053230X18011299 ↗
- Languages:
- English
- ISSNs:
- 2053-230X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0612.024200
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 7711.xml