bioRxivBiochemistryPreprint
Structure of active methyl-CoM reductase, Earth's main methane producer
Christopher J. OhmeriD, Macon J. AbernathyiD, Darya Marchany‐RiveraiD, David G. Villareal, Philipp S. SimoniD, Artem Y. LyubimoviD, Asmit BhowmickiD, Kuntal ChatterjeeiD, Hiroki MakitaiD, Vandana TiwariiD, Medhanjali DasguptaiD, Stephen J. KeableiD, David MoreauiD, Daniel W. Paley⧓iD, Nigel W. MoriartyiD, Humberto S. SancheziD, Daniel J. RosenbergiD, Leland Bruce GeeiD, Roberto Alonso‐MoriiD, Nicholas K. SauteriD, Aaron S. BrewsteriD, Uwe BergmanniD, Vittal K. YachandraiD, Aina E. CoheniD, Junko YanoiD, , Stephen Wiley RagsdaleiD
Abstract
Our work reveals the structure of the active state of Methyl-Coenzyme M Reductase (MCR), the key and rate-limiting enzyme in biological methane formation. We find large differences between the active Ni(I) and inactive Ni(II) proteins and provide insight into how nature makes and breaks the C-H bond of methane. The Ni(II)-F430 center in inactive MCR contains four planar nitrogen ligands, a lower axial glutamine oxo, and an upper axial thiolate. The Ni(I)-enzyme replaces the axial ligands with a single water. The one-electron redox change results in movement of the Ni ion and upward swing of the {beta}-lactam ring in the tetrapyrrole coupled to a domino-like protein quake through second sphere residues, inter-subunit interactions, a substrate tunnel, affecting even the dimensions of the unit cell. These structural changes lead Ni(I)-MCR to release a charge clamp that, in the Ni(II) state, locks down substrate Coenzyme B. Determining the Ni(I)-MCR structure required development of rigorous anaerobic crystallographic techniques. Validation of the MCR redox state was accomplished by in-line and parallel spectroscopic and unit cell analyses. This structure has large implications for developing technologies to limit methane emissions and efficiently produce biofuels. Methodology described here will enhance structural biology for other oxygen-sensitive enzymes.
- Citations
- 3
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Structural dynamics of the methyl-coenzyme M reductase active site are influenced by coenzyme F430 modifications
M. D. Poleto, K. D. Allen, J. A. Lemkul·bioRxiv·Jan 7, 2024
- Nickel-Sulfonate Mode of Substrate Binding for Forward and Reverse Reactions of Methyl-SCoM Reductase Suggest a Radical Mechanism Involving Long Range Electron Transfer
A. Patwardhan, R. Sarangi, … S. W. Ragsdale·bioRxiv·Jan 25, 2021
- McrD binds asymmetrically to methyl-coenzyme M reductase improving active site accessibility during assembly
G. L. Chadwick, A. M. Joiner, … D. D. Nayak·bioRxiv·Feb 1, 2023
- Methane and ethane production rates by methyl-coenzyme M reductase in cell extracts from different methanogens
V. P. T. Nguyen, S. Keller, S. Scheller·bioRxiv·Jan 8, 2024
- Atomic resolution structures of the methane-activating enzyme in anaerobic methanotrophy reveal extensive post-translational modifications.
Marie-C. Müller, Martijn Wissink, … Tristan Wagner·Nature CommunicationsPeer-reviewed·Sep 5, 2025
- Component A2 is a redox-sensitive archaeal ATPase activated by methyl-coenzyme M reductase
Sophia A. Adler, Dipti D. Nayak·Current BiologyPeer-reviewed·Jul 1, 2026