Evidence map›Paper›PMID 32148849›Full record

ArticleIUCrJ2020

3D-MiXD: 3D-printed X-ray-compatible microfluidic devices for rapid, low-consumption serial synchrotron crystallography data collection in flow.

Diana C F Monteiro, David von Stetten, Claudia Stohrer, Marta Sans, Arwen R Pearson, Gianluca Santoni, Peter van der Linden, Martin Trebbin

Abstract read
In one paragraph

Article in IUCrJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Microfluidic Devices for High-Throughput In Situ Serial Crystallography.Advances in biochemical engineering/biotechnology · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Status of macromolecular crystallography beamlines at SSRF.Journal of synchrotron radiation · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Quid Pro Flow.Journal of the American Chemical Society · 2023
    Review
  16. Article
  17. Article
  18. Article
  19. Serial femtosecond crystallography.Nature reviews. Methods primers · 2022
    Article
  20. Article
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

8 authors.

Diana C F MonteiroThe Hamburg Centre for Ultrafast Imaging, Universität Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.ORCID https://orcid.org/0000-0002-6318-7306
David von StettenEuropean Molecular Biology Laboratory, Notkestrasse 85, 22607 Hamburg, Germany.ORCID https://orcid.org/0000-0001-7906-9788
Claudia StohrerThe Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, England.ORCID https://orcid.org/0000-0001-9053-7722
Marta SansThe Hamburg Centre for Ultrafast Imaging, Universität Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.ORCID https://orcid.org/0000-0002-0102-8190
Arwen R PearsonThe Hamburg Centre for Ultrafast Imaging, Universität Hamburg, Luruper Chaussee 149, 22761 Hamburg, Germany.ORCID https://orcid.org/0000-0001-8499-7490
Gianluca SantoniEuropean Synchrotron Radiation Facility, 71 Avenue des Martyrs, CS 40220, 38043 Grenoble, France.ORCID https://orcid.org/0000-0001-6215-998X
Peter van der LindenPartnership for Soft Condensed Matter, European Synchrotron Radiation Facility, 71 Avenue des Martyrs, CS 40220, 38043 Grenoble, France.ORCID https://orcid.org/0000-0002-3481-0787
Martin TrebbinHauptman-Woodward Medical Research Institute, 700 Ellicott Street, Buffalo, NY 14203, USA.ORCID https://orcid.org/0000-0001-8278-5865

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Serial crystallography has enabled the study of complex biological questions through the determination of biomolecular structures at room temperature using low X-ray doses. Furthermore, it has enabled the study of protein dynamics by the capture of atomically resolved and time-resolved molecular movies. However, the study of many biologically relevant targets is still severely hindered by high sample consumption and lengthy data-collection times. By combining serial synchrotron crystallography (SSX) with 3D printing, a new experimental platform has been created that tackles these challenges. An affordable 3D-printed, X-ray-compatible microfluidic device (3D-MiXD) is reported that allows data to be collected from protein microcrystals in a 3D flow with very high hit and indexing rates, while keeping the sample consumption low. The miniaturized 3D-MiXD can be rapidly installed into virtually any synchrotron beamline with only minimal adjustments. This efficient collection scheme in combination with its mixing geometry paves the way for recording molecular movies at synchrotrons by mixing-triggered millisecond time-resolved SSX.

Indexed as

3D microfabrication3D-MiXD3D printingmicrofluidicsserial synchrotron crystallographystructure determination

Identifiers

PMID32148849
PMCPMC7055382

What OpenQuestion holds

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LicenceCC BY
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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.