Research group Hongyi Xu forskargrupp
Knowing the 3D atomic structures of materials and biomolecules is crucial for understanding their functions. X-ray diffraction is currently the most important technique for determination of 3D atomic structures, but requires large crystals which are often difficult to obtain
Due to the strong interactions between electrons and matter, crystals that are considered as powder in X-ray crystallography can be treated as single crystals by 3D electron diffraction methods. This enables structure determination of materials and organic molecules from micron- to nanometer-sized 3D crystals that are too small for conventional X-ray diffraction.
Over the past decades, a number of 3D ED methods have been developed for structure determination. Thanks to the recent advancement in CMOS and hybrid detector technology, it is now feasible to collect diffraction data in movie mode while continuously rotating the crystal (continuous rotation election diffraction, cRED, also known as MicroED in structural biology). Benefiting from these technological advances, structure determination can now be accomplished within few hours. Recently, fully automated serial rotation electron diffraction data collection and processing have been realized by our group. By using 3D ED and MicroED methods, we have solved more than 180 novel crystal structures of small inorganic compounds (including zeolite, MOF, COF and minerals) and organic molecules (pharmaceuticals, small organic molecules, peptides and proteins) in the past 6 years. We aim to further develop new electron crystallography methods and more importantly spread them to labs around the world.
Group members
Group managers
Hongyi Xu
Researcher
