Multi-state Ensemble Refinement for Occupancy Statistics (MEROS) in Time-Resolved X-ray Crystallography
Preprint
Abstract
Accurate determination of state occupancies is essential for interpreting the structural heterogeneity inherent in time-resolved crystallography. However, in cases of high spatial overlap between states, as commonly observed in time-resolved crystallography data, the strong correlation between occupancy and atomic displacement parameters (ADPs) can render single point estimates from standard refinement protocols unreliable. We introduce MEROS (Multi-state Ensemble Refinement for Occupancy Statistics), a pipeline that implements an ensemble refinement approach to assess the post-refinement occupancy–ADP statistics of multiple overlapping states. MEROS utilizes a Monte Carlo sampling of the parameter space, performing independent refinements from randomized starting occupancies and ADP values to empirically characterize the convergence and uncertainty of the solution. The method is implemented as a modular Python pipeline that wraps established refinement programs, ensuring compatibility with existing workflows. We demonstrate its applicability in two case studies: a two-state ligand binding model in T4 lysozyme L99A and a four-state covalent catalysis mechanism in β -lactamase CTX-M-14. MEROS provides occupancy and ADP mean values with standard deviations that directly quantify the informational content of the experimental diffraction data.Keywords
Funding Information
- Bundesministerium für Forschung, Technologie und Raumfahrt (01KI2114)
This publication has 36 references indexed in Scilit:
- Serial synchrotron crystallography for time-resolved structural biologyCurrent Opinion in Structural Biology, 2020
- β-Lactamases and β-Lactamase Inhibitors in the 21st CenturyJournal of Molecular Biology, 2019
- On the Temperature Dependence of Enzyme-Catalyzed RatesBiochemistry, 2016
- Femtosecond X-ray protein nanocrystallographyNature, 2011
- CPMG relaxation dispersion NMR experiments measuring glycine 1Hα and 13Cα chemical shifts in the ‘invisible’ excited states of proteinsJournal of Biomolecular NMR, 2009
- Application of Singular Value Decomposition to the Analysis of Time-Resolved Macromolecular X-Ray DataBiophysical Journal, 2003
- Time-Resolved Biochemical Crystallography: A Mechanistic PerspectiveChemical Reviews, 2001
- Analyzing protein functions in four dimensionsNature Structural & Molecular Biology, 2000
- Potential for biomolecular imaging with femtosecond X-ray pulsesNature, 2000
- Specificity of ligand binding in a buried nonpolar cavity of T4 lysozyme: Linkage of dynamics and structural plasticityBiochemistry, 1995