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TitleUltrathin liquid cells for microsecond time-resolved cryo-EM.
Journal, issue, pagesNat Commun, Vol. 17, Issue 1, Page 1799, Year 2026
Publish dateJan 22, 2026
AuthorsWyatt A Curtis / Jakub Wenz / Constantin R Krüger / Sarah V Barrass / Marcel Drabbels / Ulrich J Lorenz /
PubMed AbstractMicrosecond time-resolved cryo-electron microscopy promises to significantly advance our understanding of protein function by rendering cryo-electron microscopy (cryo-EM) fast enough to observe ...Microsecond time-resolved cryo-electron microscopy promises to significantly advance our understanding of protein function by rendering cryo-electron microscopy (cryo-EM) fast enough to observe proteins at work. This emerging technique involves flash melting a cryo sample with a laser beam to provide a brief time window during which dynamics are initiated. When the laser is switched off, the sample revitrifies, arresting the proteins in their transient configurations. However, observations have so far been limited to tens of microseconds only, due to the instability of the thin liquid film under laser irradiation. Here, we seal samples between two ultrathin, vapor-deposited silicon dioxide membranes to extend the observation window by an order of magnitude. These membranes not only allow for reconstructions with near-atomic spatial resolution, but can also be used to eliminate preferred particle orientation. We showcase our technology by performing a time-resolved temperature jump experiment on the 50S ribosomal subunit that provides new insights into the conformational landscape of the L1 stalk. Our experiments significantly expand the capabilities of microsecond time-resolved cryo-EM and promise to bridge the gap to the millisecond timescale, which can already be addressed with traditional approaches.
External linksNat Commun / PubMed:41571671 / PubMed Central
MethodsEM (single particle)
Resolution1.7 - 2.7 Å
Structure data

EMDB-54058: 1.7 A structure of conventional mouse heavy chain Apoferritin
Method: EM (single particle) / Resolution: 1.7 Å

EMDB-54082: 1.8 A structure of SiO2-sealed and revitrified (210 us) mouse heavy chain Apoferritin
Method: EM (single particle) / Resolution: 1.8 Å

EMDB-54136: 2.5 A structure of the E.coli 50S ribosomal subunit
Method: EM (single particle) / Resolution: 2.4 Å

EMDB-54137: 2.4 A structure of the SiO2-sealed and revitrified (30 us) E.coli 50S ribosomal subunit
Method: EM (single particle) / Resolution: 2.4 Å

EMDB-54138: 2.3 A structure of the SiO2-sealed and revitrified (150 us) E.coli 50S ribosomal subunit
Method: EM (single particle) / Resolution: 2.3 Å

EMDB-54168: 2.7 A structure of the SiO2-sealed and revitrified (300 us) E.coli 50S ribosomal subunit
Method: EM (single particle) / Resolution: 2.7 Å

Source
  • Mus musculus (house mouse)
  • Escherichia coli K-12 (bacteria)

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