Evidence map›Paper›PMID 41332690›Full record

ArticlebioRxiv : the preprint server for biology2025

Microsecond Time-Resolved Cryo-EM Based on Jet Vitrification.

Michal Haubner, Harry M Williams, Jakub Hruby, Monique S Straub, Albert Guskov, Kirill Kovalev, Marcel Drabbels, Ulrich J Lorenz

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Michal HaubnerEcole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH- 1015 Lausanne, Switzerland.ORCID 0000-0002-7320-240X
Harry M WilliamsEcole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH- 1015 Lausanne, Switzerland.ORCID 0000-0001-9108-9933
Jakub HrubyEcole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH- 1015 Lausanne, Switzerland.ORCID 0000-0002-5837-9119
Monique S StraubEcole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH- 1015 Lausanne, Switzerland.ORCID 0000-0002-7721-5048
Albert GuskovGroningen Institute for Biomolecular Sciences and Biotechnology, University of Groningen, 9747AG, Groningen, the Netherlands.ORCID 0000-0003-2340-2216
Kirill KovalevEuropean Molecular Biology Laboratory, EMBL Hamburg c/o DESY, 22607, Hamburg, Germany.ORCID 0000-0002-2229-181X
Marcel DrabbelsEcole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH- 1015 Lausanne, Switzerland.ORCID 0000-0001-8611-2684
Ulrich J LorenzEcole Polytechnique Fédérale de Lausanne (EPFL), Laboratory of Molecular Nanodynamics, CH- 1015 Lausanne, Switzerland.ORCID 0000-0002-8869-5999

Funding

Project 3 - Dynamics of latent HIV-1 reservoirs: High resolution antigenic mapping and strategies to block reboundU54AI170752 · NIAID · DUKE UNIVERSITY · PI Priyamvada Acharya · 2022 to 2026
$32.0M
NIAID NIH HHS U54 AI170752
6 · The paper itself

Abstract

Understanding and ultimately predicting the function of proteins is one of the frontiers in structural biology. This will only be possible if it becomes feasible to routinely observe proteins on the fast timescales on which they perform their tasks. Recently, laser flash melting and revitrification experiments have improved the time resolution of cryo-electron microscopy (cryo-EM) to microseconds, rendering it fast enough to observe the domain motions of proteins that are frequently linked to function. However, observations have been limited to a time window of just a few hundred microseconds. Here, we introduce time-resolved cryo-EM experiments based on jet vitrification that combine microsecond resolution with an observation window of up to seconds. We use a short laser pulse to initiate protein dynamics, and as they unfold, vitrify the sample with a jet of a liquid cryogen to arrest the dynamics at that point in time. We demonstrate that our approach affords near-atomic spatial resolution and a time resolution of 21 µs. This allows us to observe the photoinduced dynamics of the light-driven sodium pump

Identifiers

PMID41332690
PMCPMC12667775

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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.