Evidence map›Paper›PMID 37727961›Full record

ArticleIUCrJ2023

Micro-structured polymer fixed targets for serial crystallography at synchrotrons and XFELs.

Melissa Carrillo, Thomas J Mason, Agnieszka Karpik, Isabelle Martiel, Michal W Kepa, Katherine E McAuley, John H Beale, Celestino Padeste

Abstract read
In one paragraph

Article in IUCrJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
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  5. Article
  6. Article
  7. Microfluidic Devices for High-Throughput In Situ Serial Crystallography.Advances in biochemical engineering/biotechnology · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
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  15. A snapshot love story: what serial crystallography has done and will do for us.Acta crystallographica. Section D, Structural biology · 2024
    Review
  16. Article
  17. Article
  18. 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.

Melissa CarrilloPaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.ORCID 0000-0002-0744-4486
Thomas J MasonPaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.
Agnieszka KarpikPaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.
Isabelle MartielPaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.
Michal W KepaPaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.
Katherine E McAuleyPaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.
John H BealePaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.ORCID 0000-0003-1171-2428
Celestino PadestePaul Scherrer Institut, Forschungsstrasse 111, 5232 Villigen, Switzerland.ORCID 0000-0001-7577-5781

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fixed targets are a popular form of sample-delivery system used in serial crystallography at synchrotron and X-ray free-electron laser sources. They offer a wide range of sample-preparation options and are generally easy to use. The supports are typically made from silicon, quartz or polymer. Of these, currently, only silicon offers the ability to perform an aperture-aligned data collection where crystals are loaded into cavities in precise locations and sequentially rastered through, in step with the X-ray pulses. The polymer-based fixed targets have lacked the precision fabrication to enable this data-collection strategy and have been limited to directed-raster scans with crystals randomly distributed across the polymer surface. Here, the fabrication and first results from a new polymer-based fixed target, the micro-structured polymer fixed targets (MISP chips), are presented. MISP chips, like those made from silicon, have a precise array of cavities and fiducial markers. They consist of a structured polymer membrane and a stabilization frame. Crystals can be loaded into the cavities and the excess crystallization solution removed through apertures at their base. The fiducial markers allow for a rapid calculation of the aperture locations. The chips have a low X-ray background and, since they are optically transparent, also allow for an a priori analysis of crystal locations. This location mapping could, ultimately, optimize hit rates towards 100%. A black version of the MISP chip was produced to reduce light contamination for optical-pump/X-ray probe experiments. A study of the loading properties of the chips reveals that these types of fixed targets are best optimized for crystals of the order of 25 µm, but quality data can be collected from crystals as small as 5 µm. With the development of these chips, it has been proved that polymer-based fixed targets can be made with the precision required for aperture-alignment-based data-collection strategies. Further work can now be directed towards more cost-effective mass fabrication to make their use more sustainable for serial crystallography facilities and users.

Indexed as

aperturesfixed targetsfree-electron lasersmicro-structured polymer chipssample deliveryserial crystallographytime-resolved studies

Identifiers

PMID37727961
PMCPMC10619457

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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.