Evidence map›Paper›PMID 27241728›Full record

ArticleLab on a chip2016

Graphene-based microfluidics for serial crystallography.

Shuo Sui, Yuxi Wang, Kristopher W Kolewe, Vukica Srajer, Robert Henning, Jessica D Schiffman, Christos Dimitrakopoulos, Sarah L Perry

Open access · hybridAbstract readComparative StudyValidation Study
In one paragraph

Article in Lab on a chip, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.4field-weighted citation impact, top 4% of its field
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

26 citing papers in PubMed, 62 citations in OpenAlex.

  1. Microfluidic Devices for High-Throughput In Situ Serial Crystallography.Advances in biochemical engineering/biotechnology · 2026
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  18. Strategies for sample delivery for femtosecond crystallography.Acta crystallographica. Section D, Structural biology · 2019
    Review
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  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 at 3 institutions in 1 country.

Shuo SuiDepartment of Chemical Engineering, The University of Massachusetts Amherst, Amherst, MA 01003, USA. perrys@engin.umass.edu.
Yuxi WangDepartment of Chemical Engineering, The University of Massachusetts Amherst, Amherst, MA 01003, USA. perrys@engin.umass.edu.
Kristopher W KoleweDepartment of Chemical Engineering, The University of Massachusetts Amherst, Amherst, MA 01003, USA. perrys@engin.umass.edu.
Vukica SrajerBioCARS Center for Advanced Radiation Sources, The University of Chicago, Argonne, IL 60439, USA.
Robert HenningBioCARS Center for Advanced Radiation Sources, The University of Chicago, Argonne, IL 60439, USA.
Jessica D SchiffmanDepartment of Chemical Engineering, The University of Massachusetts Amherst, Amherst, MA 01003, USA. perrys@engin.umass.edu.
Christos DimitrakopoulosDepartment of Chemical Engineering, The University of Massachusetts Amherst, Amherst, MA 01003, USA. perrys@engin.umass.edu.
Sarah L PerryDepartment of Chemical Engineering, The University of Massachusetts Amherst, Amherst, MA 01003, USA. perrys@engin.umass.edu.
Amherst College · USPrimary Source · USUniversity of Massachusetts Amherst · US

Funding

CHEMISTRY-BIOLOGY INTERFACE PREDOCTORAL TRAINING GRANTST32GM008515 · NIGMS · UNIVERSITY OF MASSACHUSETTS AMHERST · PI THOMPSON, LYNMARIE K. · 1995 to 2020
$4.3M
BioCARS: A Synchrotron Structure Biology ResourceR24GM111072 · NIGMS · UNIVERSITY OF CHICAGO · PI MOFFAT, JOHN KEITH · 2013 to 2016
$2.3M
NIGMS NIH HHS R24 GM111072NIGMS NIH HHS T32 GM008515
6 · The paper itself

Abstract

Microfluidic strategies to enable the growth and subsequent serial crystallographic analysis of micro-crystals have the potential to facilitate both structural characterization and dynamic structural studies of protein targets that have been resistant to single-crystal strategies. However, adapting microfluidic crystallization platforms for micro-crystallography requires a dramatic decrease in the overall device thickness. We report a robust strategy for the straightforward incorporation of single-layer graphene into ultra-thin microfluidic devices. This architecture allows for a total material thickness of only ∼1 μm, facilitating on-chip X-ray diffraction analysis while creating a sample environment that is stable against significant water loss over several weeks. We demonstrate excellent signal-to-noise in our X-ray diffraction measurements using a 1.5 μs polychromatic X-ray exposure, and validate our approach via on-chip structure determination using hen egg white lysozyme (HEWL) as a model system. Although this work is focused on the use of graphene for protein crystallography, we anticipate that this technology should find utility in a wide range of both X-ray and other lab on a chip applications.

Indexed as

Lab-On-A-Chip DevicesCrystallographyEquipment DesignGraphiteMicrofluidicsMicroscopy, Atomic ForceMuramidaseProtein ConformationProtein StabilitySurface PropertiesX-Ray DiffractionGraphitehen egg lysozymeMuramidase

Identifiers

PMID27241728
PMCPMC4970872
OpenAlexW2401597693

What OpenQuestion holds

Textmetadata
LicenceTDM
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.