Evidence map›Paper›PMID 23385768›Full record

ArticleActa crystallographica. Section F, Structural biology and crystallization communications2013

Some practical guidelines for UV imaging in the protein crystallization laboratory.

Sebastien Desbois, Shane A Seabrook, Janet Newman

Abstract read
In one paragraph

Article in Acta crystallographica. Section F, Structural biology and crystallization communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Review
  3. Moving beyond MARCO.PloS one · 2023
    Article
  4. Inexpensive robotic system for standard and fluorescent imaging of protein crystals.Acta crystallographica. Section F, Structural biology communications · 2019
    Article
  5. Strategies for sample delivery for femtosecond crystallography.Acta crystallographica. Section D, Structural biology · 2019
    Review
  6. Improved protein-crystal identification by using 2,2,2-trichloroethanol as a fluorescence enhancer.Acta crystallographica. Section F, Structural biology communications · 2018
    Article
  7. Transmission electron microscopy for the evaluation and optimization of crystal growth.Acta crystallographica. Section D, Structural biology · 2016
    Article
  8. Article
  9. Identifying, studying and making good use of macromolecular crystals.Acta crystallographica. Section F, Structural biology communications · 2014
    Article
  10. Use of transmission electron microscopy to identify nanocrystals of challenging protein targets.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  11. Approaches to automated protein crystal harvesting.Acta crystallographica. Section F, Structural biology communications · 2014
    Article
  12. Introduction to protein crystallization.Acta crystallographica. Section F, Structural biology communications · 2014
    Review
  13. An overview of biological macromolecule crystallization.International journal of molecular sciences · 2013
    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

3 authors.

Sebastien DesboisCSIRO Materials, Science and Engineering, 343 Royal Parade, Parkville, VIC 3052, Australia.
Shane A Seabrook
Janet Newman

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput imaging of protein crystallization experiments with ultraviolet (UV) light has recently become commercially available and can enable crystallographers to differentiate between crystals of protein and those of salt, as the visualization of protein crystals is based on intrinsic tryptophan fluorescence. Unfortunately, UV imaging is not a panacea, as some protein crystals will not fluoresce under UV excitation and some salt crystals are UV-fluorescently active. As a new technology, there is little experience within the general community on how to use this technology effectively and what caveats to look out for. Here, an attempt is made to identify some of the common problems that may arise using UV-imaging technology by examining test proteins, common crystallization reagents and a range of proteins by assessing their UV-Vis absorbance spectra. Some pointers are offered as to which systems may not be appropriate for this methodology.

Indexed as

Ultraviolet RaysBuffersCrystallizationDNAFluorescenceLaboratoriesProteinsSpectrophotometry, UltravioletTryptophanBuffersDNAProteinsTryptophanUV imaging

Identifiers

PMID23385768
PMCPMC3564629

What OpenQuestion holds

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Registered trials

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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.