
Simplified Cryo-EM Structure Determination
Streamline projects with optimized cryo-EM workflows
Cryogenic Electron Microscopy (cryo-EM) uses sophisticated Transmission Electron Microscopes (TEM) to directly visualize biological samples. It is particularly advantageous when studying challenging biological systems, such as macromolecular complexes in different functional states. Cryo-EM can overcome the challenges of traditional methods, providing structural information for samples in near-native states.
With cryo-EM, our structural biologists can answer questions regarding the interactions of small molecules with the chosen target and suggest ways to help design and optimize drug candidates, supporting a structure-based drug design approach.
Our Infrastructure
We have six microscopes across our San Diego and Boston sites, including two Titan Krios and four Glacios instruments. This provides the most comprehensive industrial access in North America. We deploy negative stain and cryogenic techniques along with proprietary vitrification workflows to maximize the chance of success for your structural study.
We support both on-site and co-localized high speed computing resources consisting of more than 500 processing cores, 50 GPUs, and six petabytes of storage space, all located within secure facilities behind multiple high availability firewalls and following NIST security guidelines.

The Imaging Workflow
Sample to Structure in 2 to 4 Weeks

Tailored Cryo-EM Solutions
Epitope Mapping
Gain near-atomic resolution results detailing epitope/paratope interactions of antibody-antigen complexes in as little as 2 weeks.
Off Target hERG Structure Determination
We provide a 3D structure reconstruction of detergent solubilized hERG in complex with your ligand of interest.
Off Target CYP3A4 Structure Determination
We provide a 3D structure reconstruction of CYP3A4 in complex with your ligand of interest.
DMPK Optimization of Human Serum Albumin (HSA) by Structure Determination
We provide a 3D structure reconstruction of HSA in complex with your ligand of interest.
Our Stats
3D structures determined by cryo-EM
of protein structures solved at 3.5 Å or better resolution
Membrane proteins solved
years of cryo-EM experience

