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Microcrystal electron diffraction sample preparation workflow
Microcrystal electron diffraction (MicroED) enables fast, high-resolution, structural determination of small molecules and proteins. Atomic details can be extracted from individual nanocrystals (<200 nm in depth), even in a heterogeneous mixture. Data is acquired by cryo-TEM, using electrons as the incident beam. Since MicroED is a diffraction technique, samples need to be crystallized. Sample preparation for MicroED varies between small molecule and protein samples. Protein crystal can be prepared using the same methods that are found in X-ray crystallography. Learn more about our MicroED sample preparation workflows and solutions below.
Protein sample preparation for MicroED
- Step 1: Protein expression
- Step 2: Protein purification
- Step 3: Vitrification
- Step 4: Milling
Protein expression
Using the right protein expression system for cryo-EM is critical to success. Consider protein solubility, functionality, purification speed, and yield when choosing an expression system. We offer a wide selection of protein expression systems to suit your research needs. Check out our protein expression system tool to find the right products for your research work.
Microcrystal electron diffraction small molecule preparation
Small molecule crystals are usually dry and can often be prepared at room temperature. Mechanical grinding can easily be used to reduce the size of large crystals, or the molecules can simply be crystallized spontaneously out of solution using evaporation. MicroED necessitates thin crystals (<200 nm) but samples can be cut or milled from larger crystals using a focused ion beam (FIB), if necessary. Note that crystals thicker than 200 nm have increased secondary scattering, which convolutes the data.
Microcrystal electron diffraction sample preparation resources
For Research Use Only. Not for use in diagnostic procedures.