Evidence map›Paper›PMID 37500774›Full record

ArticleNature nanotechnology2023

Enzyme-less nanopore detection of post-translational modifications within long polypeptides.

Pablo Martin-Baniandres, Wei-Hsuan Lan, Stephanie Board, Mercedes Romero-Ruiz, Sergi Garcia-Manyes, Yujia Qing, Hagan Bayley

Open access · hybridAbstract read
In one paragraph

Article in Nature nanotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
13.4field-weighted citation impact, top 1% 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

60 citing papers in PubMed, 122 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Biosensing With Nanofluidics.Exploration (Beijing, China) · 2026
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Proteoforms as the true units of physiological function.European journal of applied physiology · 2026
    Review
  13. Review
  14. Article
  15. Nanopore-Based Detection of Protein Posttranslational Modifications.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  16. Engineering a Monomeric Nanopore Scaffold for Multiplexed Protein Detection.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  17. Expression and Purification of CytK Nanopores.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Pablo Martin-Baniandres *Department of Chemistry, University of Oxford, Oxford, UK.
Wei-Hsuan Lan *Department of Chemistry, University of Oxford, Oxford, UK.
Stephanie BoardDepartment of Physics, Randall Centre for Cell and Molecular Biophysics and London Centre for Nanotechnology, King's College London, London, UK.ORCID 0000-0002-1189-8173
Mercedes Romero-RuizDepartment of Chemistry, University of Oxford, Oxford, UK.ORCID 0000-0002-3362-9468
Sergi Garcia-ManyesDepartment of Physics, Randall Centre for Cell and Molecular Biophysics and London Centre for Nanotechnology, King's College London, London, UK.ORCID 0000-0001-5140-2606
Yujia QingDepartment of Chemistry, University of Oxford, Oxford, UK. yujia.qing@chem.ox.ac.uk.ORCID 0000-0002-2110-4269
Hagan BayleyDepartment of Chemistry, University of Oxford, Oxford, UK. hagan.bayley@chem.ox.ac.uk.ORCID 0000-0003-2499-6116
University of Oxford · GBKing's College London · GB

Funding

Wellcome Trust FC001002
6 · The paper itself

Abstract

Means to analyse cellular proteins and their millions of variants at the single-molecule level would uncover substantial information previously unknown to biology. Nanopore technology, which underpins long-read DNA and RNA sequencing, holds potential for full-length proteoform identification. We use electro-osmosis in an engineered charge-selective nanopore for the non-enzymatic capture, unfolding and translocation of individual polypeptides of more than 1,200 residues. Unlabelled thioredoxin polyproteins undergo transport through the nanopore, with directional co-translocational unfolding occurring unit by unit from either the C or N terminus. Chaotropic reagents at non-denaturing concentrations accelerate the analysis. By monitoring the ionic current flowing through the nanopore, we locate post-translational modifications deep within the polypeptide chains, laying the groundwork for compiling inventories of the proteoforms in cells and tissues.

Indexed as

NanoporesDNAPeptidesProtein Processing, Post-TranslationalDNAPeptides

Identifiers

PMID37500774
PMCPMC10656283
OpenAlexW4385302448

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.