Evidence map›Paper›PMID 39024453›Full record

ArticleScience (New York, N.Y.)2024

Sculpting conducting nanopore size and shape through de novo protein design.

Samuel Berhanu, Sagardip Majumder, Thomas Müntener, James Whitehouse, Carolin Berner, Asim K Bera, Alex Kang, Binyong Liang, Nasir Khan, Banumathi Sankaran and 6 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Sculpting semisynthetic conducting protein pores by de novo design.Nature structural & molecular biology · 2026
    Article
  2. De novo design of semisynthetic conduction pores.Nature structural & molecular biology · 2026
    Article
  3. Review
  4. Generative design of programmable asymmetric β-barrel nanopores.bioRxiv : the preprint server for biology · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Negative design enables cell-free expression and folding of designed transmembrane β-barrels.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  9. Structures of folding intermediates on BAM show diverse substrates fold by a conserved mechanism.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  10. Review
  11. Review
  12. Review
  13. β-barrels from short macrocyclic peptides.Chemical communications (Cambridge, England) · 2026
    Article
  14. Protein engineering: status report.Protein engineering, design & selection : PEDS · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Samuel Berhanu *Department of Biochemistry, The University of Washington, Seattle, WA, USA.ORCID 0000-0001-6252-1301
Sagardip Majumder *Department of Biochemistry, The University of Washington, Seattle, WA, USA.ORCID 0000-0002-4736-6945
Thomas Müntener *Biozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0001-5508-1117
James Whitehouse *Astbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT.ORCID 0000-0003-0088-4312
Carolin BernerStructural Biology Brussel, Vrije Universiteit Brussel, Brussels, Belgium.
Asim K BeraDepartment of Biochemistry, The University of Washington, Seattle, WA, USA.ORCID 0000-0001-9473-2912
Alex KangDepartment of Biochemistry, The University of Washington, Seattle, WA, USA.ORCID 0000-0001-5487-0499
Binyong LiangDepartment of Molecular Physiology and Biological Physics and Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA, USA.ORCID 0000-0001-9347-4958
Nasir KhanAstbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT.ORCID 0000-0002-1834-2485
Banumathi SankaranMolecular Biophysics and Integrated Bioimaging Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.ORCID 0000-0002-3266-8131
Lukas K TammDepartment of Molecular Physiology and Biological Physics and Center for Membrane and Cell Physiology, University of Virginia, Charlottesville, VA, USA.ORCID 0000-0002-1674-4464
David J BrockwellAstbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT.ORCID 0000-0002-0802-5937
Sebastian HillerBiozentrum, University of Basel, Basel, Switzerland.ORCID 0000-0002-6709-4684
Sheena E RadfordAstbury Centre for Structural Molecular Biology, School of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT.ORCID 0000-0002-3079-8039
David BakerDepartment of Biochemistry, The University of Washington, Seattle, WA, USA.ORCID 0000-0001-7896-6217
Anastassia A VorobievaStructural Biology Brussel, Vrije Universiteit Brussel, Brussels, Belgium.ORCID 0000-0001-5554-1398

Funding

User Training and OutreachP30GM124169 · NIGMS · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI PAUL David ADAMS, Gregory L Hura · 2017 to 2026
$28.6M
Structural Dynamics of the Exocytotic Fusion Machine in Neurons.P01GM072694 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI TAMM, LUKAS K · 2005 to 2021
$17.4M
NIGMS NIH HHS P01 GM072694NIGMS NIH HHS P30 GM124169
6 · The paper itself

Abstract

Transmembrane β-barrels have considerable potential for a broad range of sensing applications. Current engineering approaches for nanopore sensors are limited to naturally occurring channels, which provide suboptimal starting points. By contrast, de novo protein design can in principle create an unlimited number of new nanopores with any desired properties. Here we describe a general approach to designing transmembrane β-barrel pores with different diameters and pore geometries. Nuclear magnetic resonance and crystallographic characterization show that the designs are stably folded with structures resembling those of the design models. The designs have distinct conductances that correlate with their pore diameter, ranging from 110 picosiemens (~0.5 nanometer pore diameter) to 430 picosiemens (~1.1 nanometer pore diameter). Our approach opens the door to the custom design of transmembrane nanopores for sensing and sequencing applications.

Indexed as

NanoporesProtein EngineeringCrystallography, X-RayModels, MolecularNuclear Magnetic Resonance, BiomolecularProtein Conformation, beta-StrandProtein Folding

Identifiers

PMID39024453
PMCPMC11549965

What OpenQuestion holds

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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.