Laue Diffractometer

Mission Statement
Biochemistry, biotechnology and drug design at the atomic scale
Neutron macromolecular crystallography (NMX) provides unparalleled insight into the molecular mechanisms of biological macromolecules, resolving fundamental questions about enzyme catalysis and enabling new strategies for rational drug design. As the only experimental technique capable of directly determining the positions of hydrogen atoms in biomacromolecules, NMX reveals critical details of hydrogen bonding, protonation states, and proton transfer that underpin biochemical reactions and molecular recognition. With its high-resolution capabilities, IMAGINE-X will enable researchers to investigate proteins, nucleic acids, and their complexes at an unprecedented level of functional detail. These studies will elucidate enzyme mechanisms, guide the engineering of improved industrial enzymes, reveal the molecular basis of disease, and accelerate the development of next-generation therapeutics, vaccines, and other structure-based drug design strategies.
Instrument Description
CG-4D’s IMAGINE-X instrument is a state-of-the-art single-crystal diffractometer that provides atomic resolution information on inorganic, organic, metallo-organic, and macromolecular single crystals that enables their chemical, physical, and biological structure and function to be understood. IMAGINE-X benefits communities with interest in pharmaceuticals, minerals and materials, small molecules, molecular organo-metallic complexes and metal-organic frameworks and enables the neutron crystal structure of oligonucleotides and proteins to be determined at near atomic resolutions (1.5 Å).
The instrument has undergone significant upgrade with the design and installation of a new continuously operating dynamic nuclear polarization (DNP) system for nuclear polarization, a new suite of 74 silicon photo multiplier (SiPM) Anger camera detectors suite and new polarized optics and spin-flipper to control the spin state of each event. The new DNP system enables tunable control of hydrogen neutron scattering cross sections in situ within biological crystals during experiments, which will provide order of magnitude enhancements in data collection and in the visibility of hydrogen atoms in the resulting protein structures. The polarized incident beam option also provides enhanced sensitivity for probing weak magnetic scattering signals from magnetic materials.
Applications
Macromolecular structure and function
- Hydrogen atoms in proteins
- Enzyme mechanisms and enzyme engineering
- Ligand complexes
- Protein-protein and protein-nucleic acid complexes
- Structure-assisted drug design
Supra-Molecular Crystallography
- Single molecule magnets (SMMs)
- Metal-organic-frameworks (MOFs)
- Polyoxometalates (POMs)
- Phase transitions
- Magnetic structures
Sample Environment: Materials under Extreme Environment
- DNP – 5T magnetic field and 1K cryostat
Specifications
| Flux | ~107 n/s/cm2 |
| Cross section | 2.0 x 3.2 mm |
| Wavelengths minimum | 2.0, 2.8, 3.3 Å |
| Wavelengths maximum | 3.0, 4.0, 4.5 Å |
| Detector | 74 silicon photo multiplier (SiPM) Anger cameras |
| Detector size | 2pi opening angle |
| Pixel size | 500 µm |
| Sample-to-detector distance | Variable – 350-600 mm |
| Goniometer | Multi-axis Kappa, Phi, Omega cryo-goniometer operating at 1K |
IMAGINE-X Instrument Team
Please select link below to email the instrument team. Be sure to include your name and email address.
Contact the IMAGINE-X Instrument Team
Andrey Kovalevski – Instrument Scientist
Dean Myles – Instrument Scientist
Flora Meilleur – Instrument Scientist
Yaohua Liu – Instrument Scientist
Zachary Morgan – Computational Instrument Scientist
Malcolm Cochran – Scientific Associate
Emily Kroll – Scientific Associate
Schroder G.C.; Crichlow G.V.; Jablonowski E.; Pantouris G.; Nix J.C.; Chayen N.; Meilleur F.; Lolis E.J. “Identification of a key water molecule involved in the macrophage migration inhibitory factor-catalyzed tautomerization of para-hydroxyphenylpyruvate using neutron crystallography”, Protein Science, 35, e70666, 2026
Fu S.; Li F.; Pierce J.; Giuliano D.; Bolton J.; Leiner J.; Myles D.A.; Jiang C. “A high-efficiency cryogenic neutron spin flipper for IMAGINE-X at the high flux isotope reactor”, Review of Scientific Instruments, 97, 073301, 2026
Gerlits O.; Collins A.; Kovalevsky A. “Structural insights into RNase H catalytic mechanism from room-temperature X-ray and neutron crystallography of apo- and RNA/DNA hybrid-bound enzyme”, Current Research in Structural Biology, 11, 100188, 2026
Drago V.; Phillips R.S.; Kovalevsky A. “Mutation of active site glutamate in serine hydroxymethyltransferase allows trapping a reactive intermediate: a combined neutron and X-ray crystallography study”, RSC Advances, 16, 22600-22609, 2026
Lin J.; Gerlits O.; Kneller D.W.; Weiss K.; Coates L.; Clarke J.L.; Hix M.A.; Effah S.Y.; Kovalevsky A.; Walker A.R.; Wilson M.A. “Environmental Contributions to Proton Sharing in Protein Low-Barrier Hydrogen Bonds”, Biochemistry, 65, 764–778, 2026
Drago V.; Blakeley M.P.; Phillips R.S.; Kovalevsky A. “Neutron diffraction reveals protonation states in pyridoxal-5′-phosphate-free and glycine external aldimine-bound serine hydroxymethyltransferase”, FEBS Journal, 293, 582-597, 2026
Yurov M.; Pierce J. “The Dynamic Nuclear Polarization Program at ORNL”, 2024
Drago V.; Devos J.M.; Blakeley M.P.; Forsyth V.T.; Parks J.M.; Kovalevsky A.; Mueser T.C. “Neutron diffraction from a microgravity-grown crystal reveals the active site hydrogens of the internal aldimine form of tryptophan synthase”, Cell Reports Physical Science, 5, 101827, 2024
Drago V.; Campos C.; Hooper M.; Collins A.; Gerlits O.; Weiss K.; Blakeley M.P.; Phillips R.S.; Kovalevsky A. “Revealing protonation states and tracking substrate in serine hydroxymethyltransferase with room-temperature X-ray and neutron crystallography”, Communications Chemistry, 6, 162, 2023

Capabilities of the IMAGINE-X Instrument
Macromolecular crystallography
- Unit cell dimension < 150 Å
- Crystal volume > 0.1 mm3
- Resolution ≥ 1.4 Å
- Room temperature data collection
- DNP data collection at 5T and 1K.
Instrument Status
The IMAGINE instrument was decommissioned in June 2025.
The dynamic nuclear polarization (DNP)-enhanced single crystal diffractometer, IMAGINE-X, is under construction.
Related Research Highlights
December 1, 2020
Mapping Hydrogen Atoms in SARS-CoV-2 Main Protease
April 2, 2020
De novo Design of a Homo-Trimeric
January 17, 2020
Low-Barrier Hydrogen Bonds Improve Enzyme Interaction