Evidence map›Paper›PMID 24914149›Full record

ArticlePhilosophical transactions of the Royal Society of London. Series B, Biological sciences2014

Microcrystallization techniques for serial femtosecond crystallography using photosystem II from Thermosynechococcus elongatus as a model system.

Christopher Kupitz, Ingo Grotjohann, Chelsie E Conrad, Shatabdi Roy-Chowdhury, Raimund Fromme, Petra Fromme

Abstract read
In one paragraph

Article in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

  1. Review
  2. Article
  3. Preparing for successful protein crystallization experiments.Acta crystallographica. Section F, Structural biology communications · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Serial femtosecond crystallography.Nature reviews. Methods primers · 2022
    Article
  12. Ultrafast isolated molecule imaging without crystallization.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Homogeneous batch micro-crystallization of proteins from ammonium sulfate.Acta crystallographica. Section D, Structural biology · 2021
    Article
  15. Macromolecular phasing using diffraction from multiple crystal forms.Acta crystallographica. Section A, Foundations and advances · 2021
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Strategies for sample delivery for femtosecond crystallography.Acta crystallographica. Section D, Structural biology · 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

6 authors.

Christopher KupitzDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85281, USA.
Ingo GrotjohannDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85281, USA.
Chelsie E ConradDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85281, USA.
Shatabdi Roy-ChowdhuryDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85281, USA.
Raimund FrommeDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85281, USA.
Petra FrommeDepartment of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85281, USA petra.fromme@asu.edu.

Funding

Center for the Rational Design of Membrane Protein CrystallographyU54GM094599 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI FROMME, PETRA · 2010 to 2014
$6.8M
Femtosecond nano-crystallography of membrane proteinsR01GM095583 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI FROMME, PETRA · 2010 to 2023
$4.3M
NIGMS NIH HHS R01 GM095583NIGMS NIH HHS U54 GM094599
6 · The paper itself

Abstract

Serial femtosecond crystallography (SFX) is a new emerging method, where X-ray diffraction data are collected from a fully hydrated stream of nano- or microcrystals of biomolecules in their mother liquor using high-energy, X-ray free-electron lasers. The success of SFX experiments strongly depends on the ability to grow large amounts of well-ordered nano/microcrystals of homogeneous size distribution. While methods to grow large single crystals have been extensively explored in the past, method developments to grow nano/microcrystals in sufficient amounts for SFX experiments are still in their infancy. Here, we describe and compare three methods (batch, free interface diffusion (FID) and FID centrifugation) for growth of nano/microcrystals for time-resolved SFX experiments using the large membrane protein complex photosystem II as a model system.

Indexed as

ElectronsLasersCrystallizationCrystallography, X-RayCyanobacteriaNanoparticlesPhotosystem II Protein ComplexProtein ConformationX-Ray DiffractionPhotosystem II Protein Complexcrystallizationfemtosecond crystallographyfree-electron lasernanocrystalsphotosystem II

Identifiers

PMID24914149
PMCPMC4052858

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.