Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Cryo-electron Microscopy01:28

Cryo-electron Microscopy

3.3K
Conventional electron microscopy (EM) involves dehydration, fixation, and staining of biological samples, which distorts the native state of biological molecules and results in several artifacts. Also, the high-energy electron beam damages the sample and makes it difficult to obtain high-resolution images. These issues can be addressed using cryo-EM, which uses frozen samples and gentler electron beams. The technique was developed by Jacques Dubochet, Joachim Frank, and Richard Henderson, for...
3.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Characterization and modulation of human insulin degrading enzyme conformational dynamics to control enzyme activity.

eLife·2026
Same author

A bacteriophytochrome Pr/Pfr heterodimer studied through single-particle time-resolved cryo-electron microscopy.

Communications chemistry·2026
Same author

Characterization Standard for <i>In-situ</i> Cryo-electron Tomography.

bioRxiv : the preprint server for biology·2026
Same author

AreTomoLive: automated reconstruction of comprehensively corrected and denoised cryo-electron tomograms in real time and at high throughput.

Nature methods·2026
Same author

copick: An open dataset interface and toolkit for collaborative annotation and analysis of cryo-electron tomography data.

Protein science : a publication of the Protein Society·2026
Same author

Cryo-EM Structure of Human ATAD2B Reveals a Hexameric Organization Contributes to ATPase Activity and Substrate Coordination.

bioRxiv : the preprint server for biology·2026

Related Experiment Video

Updated: Jul 10, 2025

User-friendly, High-throughput, and Fully Automated Data Acquisition Software for Single-particle Cryo-electron Microscopy
07:56

User-friendly, High-throughput, and Fully Automated Data Acquisition Software for Single-particle Cryo-electron Microscopy

Published on: July 29, 2021

3.6K

Automated pipelines for rapid evaluation during cryoEM data acquisition.

Joshua H Mendez1, Eugene Y D Chua1, Mohammadreza Paraan1

  • 1Simons Electron Microscopy Center, New York Structural Biology Center, New York, NY, USA.

Current Opinion in Structural Biology
|November 21, 2023
PubMed
Summary

On-the-fly data processing in cryo-electron microscopy (cryoEM) speeds up biomolecular structure determination. This review assesses real-time software to enhance data quality and collection efficiency for researchers.

More Related Videos

Strategies for Optimization of Cryogenic Electron Tomography Data Acquisition
08:16

Strategies for Optimization of Cryogenic Electron Tomography Data Acquisition

Published on: March 19, 2021

4.5K
Single Particle Cryo-Electron Microscopy: From Sample to Structure
11:52

Single Particle Cryo-Electron Microscopy: From Sample to Structure

Published on: May 29, 2021

8.6K

Related Experiment Videos

Last Updated: Jul 10, 2025

User-friendly, High-throughput, and Fully Automated Data Acquisition Software for Single-particle Cryo-electron Microscopy
07:56

User-friendly, High-throughput, and Fully Automated Data Acquisition Software for Single-particle Cryo-electron Microscopy

Published on: July 29, 2021

3.6K
Strategies for Optimization of Cryogenic Electron Tomography Data Acquisition
08:16

Strategies for Optimization of Cryogenic Electron Tomography Data Acquisition

Published on: March 19, 2021

4.5K
Single Particle Cryo-Electron Microscopy: From Sample to Structure
11:52

Single Particle Cryo-Electron Microscopy: From Sample to Structure

Published on: May 29, 2021

8.6K

Area of Science:

  • Structural biology
  • Biophysics
  • Biochemistry

Background:

  • Cryo-electron microscopy (cryoEM) is crucial for high-resolution biomolecular structure determination.
  • Data processing in cryoEM is often time-consuming, posing a challenge for new researchers.
  • On-the-fly processing software aims to automate tasks like motion correction and CTF estimation.

Purpose of the Study:

  • To review on-the-fly data processing software for cryoEM.
  • To identify metrics for assessing data quality during data collection.
  • To evaluate the features and performance of ideal on-the-fly processing systems.

Main Methods:

  • Literature review of existing on-the-fly cryoEM data processing software.
  • Definition of minimal metrics for real-time data quality assessment.
  • Comparative analysis of three selected on-the-fly processing software packages.

Main Results:

  • On-the-fly processing significantly improves data collection efficiency and instrument productivity.
  • Software packages vary in performance, computational needs, and automation levels.
  • Key metrics for real-time quality control were identified.

Conclusions:

  • Automated on-the-fly processing is vital for efficient cryoEM data acquisition.
  • Selecting appropriate software requires consideration of performance and computational resources.
  • Standardized quality metrics aid in optimizing cryoEM data collection.