CCeMMP Seminar Series Dr Max Clabbers – Sept 2023
Recent Advances in Microcrystal Electron Diffraction
Membrane protein crystallography, direct electron detection, and ab initio phasing
Structure determination in membrane protein crystallography is often hampered by failed crystallization attempts that can be notoriously difficult and typically require the use of highly viscous lipidic mesophases to facilitate crystallization by mimicking the native lipid bilayer. This complicates sample handling, the crystals often are only very small, and they are difficult to locate and access from the crystallization matrix they are embedded in. MicroED is a cryo-EM method suitable for structure determination of small microcrystals that are beyond the reach of conventional X-ray crystallography. Here, we demonstrate that fluorescently labeled crystals of a G protein-coupled receptor (GPCR) grown in lipidic cubic phase (LCP) can successfully be localized and machined into thin lamellae using plasma FIB and scanning electron microscopy (pFIB/SEM) with an integrated fluorescence light microscopy (iFLM) module. High-quality MicroED data were collected using electron counting on a direct electron detector, resolving the structure of the human adenosine receptor and revealing the bound ligand. Optimizing the sample preparation was key in deriving a structural model, as well as improvements made in both data quality and resolution employing direct electron detection. Electron counting data collection was feasible after significantly lowering the exposure to ensure a linear response of the camera and minimize coincidence loss. Furthermore, electron counting enabled ab initio phasing of two macromolecular structures, triclinic lysozyme at 0.87 Å and proteinase K at 1.5 Å resolution, and allowed visualization of individual hydrogen atom positions at sub-atomic resolution. Taken together, these advances in MicroED methods open up a new path for routine high-quality structure determination of difficult to crystallize membrane proteins and create novel opportunities for drug discovery.
Dr. Max Clabbers
Howard Hughes Medical Institute
Department of Biological Chemistry
David Geffen School of Medicine