Evidence map›Paper›PMID 21575566›Full record

ReviewBiophysical journal2011

Reaching the information limit in cryo-EM of biological macromolecules: experimental aspects.

Robert M Glaeser, Richard J Hall

Abstract readReview
In one paragraph

Review in Biophysical journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed.

  1. Review
  2. Article
  3. Membrane protein structure and dynamics probed by MicroED.Biochemical Society transactions · 2026
    Review
  4. Article
  5. Article
  6. Liquid Phase Biological Electron Microscopy: Many Published Results and Claimed Benefits Are Fantasy, Not Fact.Microscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Cryo-EM of the injectisome and type III secretion systems.Current opinion in structural biology · 2022
    Review
  13. Article
  14. Quantitative Cryo-Electron Tomography.Frontiers in molecular biosciences · 2022
    Review
  15. Review
  16. Progress Towards CryoEM: Negative-Stain Procedures for Biological Samples.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  17. Article
  18. Developments, applications, and prospects of cryo-electron microscopy.Protein science : a publication of the Protein Society · 2020
    Review
  19. Review
  20. Single-particle reconstruction statistics: a diagnostic tool in solving biomolecular structures by cryo-EM.Acta crystallographica. Section F, Structural biology communications · 2019
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Robert M GlaeserLife Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, California, USA. rmglaeser@lbl.gov
Richard J Hall

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although cryo-electron microscopy (cryo-EM) of biological macromolecules has made important advances in the past few years, the level of current technical performance is still well below what the physics of electron scattering would allow. It should be possible, for example, to use cryo-EM to solve protein structures at atomic resolution for particle sizes well below 80 kDa, but currently this has been achieved only for particles at least 10 times larger than that. In this review, we first examine some of the reasons for this large gap in performance. We then give an overview of work that is currently in progress to 1), improve the signal/noise ratio for area detectors; 2), improve the signal transfer between the scattered electrons and the corresponding images; and 3), reduce the extent to which beam-induced movement causes a steep fall-off of signal at high resolution. In each case, there is substantial reason to think that cryo-EM can indeed be made to approach the estimated physical limits.

Indexed as

Cryoelectron MicroscopyFourier AnalysisMacromolecular SubstancesModels, MolecularMotionMacromolecular Substances

Identifiers

PMID21575566
PMCPMC3093552

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.