Evidence map›Paper›PMID 32651368›Full record

ArticleNature communications2020

Modular microfluidics enables kinetic insight from time-resolved cryo-EM.

Märt-Erik Mäeots, Byungjin Lee, Andrea Nans, Seung-Geun Jeong, Mohammad M N Esfahani, Shan Ding, Daniel J Smith, Chang-Soo Lee, Sung Sik Lee, Matthias Peter and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
10.6field-weighted citation impact, top 2% 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

55 citing papers in PubMed, 103 citations in OpenAlex.

  1. Article
  2. Article
  3. A Plug-and-Play Volume Minimizing Micromixer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Microfluidic Devices for High-Throughput In Situ Serial Crystallography.Advances in biochemical engineering/biotechnology · 2026
    Review
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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

11 authors at 4 institutions in 3 countries.

Märt-Erik Mäeots *Institute of Biochemistry, Department of Biology, ETH Zurich, Otto-Stern-Weg 3, 8093, Zurich, Switzerland.
Byungjin Lee *Department of Chemical Engineering and Applied Chemistry, Chungnam National University, Yuseong-Gu, Daejeon, 305-764, Republic of Korea.
Andrea NansStructural Biology Scientific Technology Platform, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK.ORCID http://orcid.org/0000-0002-3791-2447
Seung-Geun JeongDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Yuseong-Gu, Daejeon, 305-764, Republic of Korea.ORCID http://orcid.org/0000-0003-1968-4468
Mohammad M N EsfahaniThe Visual Biochemistry Laboratory, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK.
Shan DingThe Visual Biochemistry Laboratory, The Francis Crick Institute, 1 Midland Road, NW1 1AT, London, UK.
Daniel J SmithInstitute of Biochemistry, Department of Biology, ETH Zurich, Otto-Stern-Weg 3, 8093, Zurich, Switzerland.
Chang-Soo LeeDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Yuseong-Gu, Daejeon, 305-764, Republic of Korea. rhadum@cnu.ac.kr.ORCID http://orcid.org/0000-0003-3789-2412
Sung Sik LeeInstitute of Biochemistry, Department of Biology, ETH Zurich, Otto-Stern-Weg 3, 8093, Zurich, Switzerland. leesu@ethz.ch.ORCID http://orcid.org/0000-0001-9267-232X
Matthias PeterInstitute of Biochemistry, Department of Biology, ETH Zurich, Otto-Stern-Weg 3, 8093, Zurich, Switzerland. matthias.peter@bc.biol.ethz.ch.ORCID http://orcid.org/0000-0002-2160-6824
Radoslav I EnchevInstitute of Biochemistry, Department of Biology, ETH Zurich, Otto-Stern-Weg 3, 8093, Zurich, Switzerland. radoslav.enchev@crick.ac.uk.ORCID http://orcid.org/0000-0003-1873-0880
The Francis Crick Institute · GBChungnam National University · KRETH Zurich · CHUniversity of Zurich · CH

Funding

Cancer Research UK FC001597Medical Research Council FC001597Wellcome Trust FC001597
6 · The paper itself

Abstract

Mechanistic understanding of biochemical reactions requires structural and kinetic characterization of the underlying chemical processes. However, no single experimental technique can provide this information in a broadly applicable manner and thus structural studies of static macromolecules are often complemented by biophysical analysis. Moreover, the common strategy of utilizing mutants or crosslinking probes to stabilize intermediates is prone to trapping off-pathway artefacts and precludes determining the order of molecular events. Here we report a time-resolved sample preparation method for cryo-electron microscopy (trEM) using a modular microfluidic device, featuring a 3D-mixing unit and variable delay lines that enables automated, fast, and blot-free sample vitrification. This approach not only preserves high-resolution structural detail but also substantially improves sample integrity and protein distribution across the vitreous ice. We validate the method by visualising reaction intermediates of early RecA filament growth across three orders of magnitude on sub-second timescales. The trEM method reported here is versatile, reproducible, and readily adaptable to a broad spectrum of fundamental questions in biology.

Indexed as

BiophysicsCryoelectron MicroscopyKineticsMicrofluidicsMicroscopy, Fluorescence

Identifiers

PMID32651368
PMCPMC7351747
OpenAlexW3042080880

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.