Nanofluidic chips for cryo-EM structure determination from picoliter sample volumes

Elife. 2022 Jan 21:11:e72629. doi: 10.7554/eLife.72629.

Abstract

Cryogenic electron microscopy has become an essential tool for structure determination of biological macromolecules. In practice, the difficulty to reliably prepare samples with uniform ice thickness still represents a barrier for routine high-resolution imaging and limits the current throughput of the technique. We show that a nanofluidic sample support with well-defined geometry can be used to prepare cryo-EM specimens with reproducible ice thickness from picoliter sample volumes. The sample solution is contained in electron-transparent nanochannels that provide uniform thickness gradients without further optimisation and eliminate the potentially destructive air-water interface. We demonstrate the possibility to perform high-resolution structure determination with three standard protein specimens. Nanofabricated sample supports bear potential to automate the cryo-EM workflow, and to explore new frontiers for cryo-EM applications such as time-resolved imaging and high-throughput screening.

Keywords: MEMS; cryo-EM; molecular biophysics; nanofluidics; none; specimen preparation; structural biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cryoelectron Microscopy / instrumentation
  • Cryoelectron Microscopy / methods*
  • Microfluidics / instrumentation*
  • Microfluidics / methods*
  • Proteasome Endopeptidase Complex
  • Protein Array Analysis / methods*
  • Specimen Handling / instrumentation*
  • Specimen Handling / methods*
  • Water / chemistry

Substances

  • Water
  • Proteasome Endopeptidase Complex

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.