Evidence map›Paper›PMID 42542535›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Nanopore-Based Detection of Protein Posttranslational Modifications.

Meng-Yin Li, Yan Gao, Jie Jiang, Yi-Tao Long

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Article in Methods in molecular biology (Clifton, N.J.), 2026. 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
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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

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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

4 authors.

Meng-Yin LiSchool of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China. mengyinli@nju.edu.cn.
Yan GaoSchool of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China.
Jie JiangSchool of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China.
Yi-Tao LongSchool of Chemistry and Chemical Engineering, Nanjing University, Nanjing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Posttranslational modifications (PTMs) are crucial regulators of protein functions, localization, and interactions, contributing to nearly all aspects of cellular physiology. Conventional analytical approaches, such as mass spectrometry (MS), have achieved high sensitivity and coverage, yet they often require complex sample preparation, enrichment, and high-end instrumentation. Nanopore has emerged as a promising single-molecule approach for PTM detection, offering label-free, high-throughput, and potentially portable analysis capabilities. Despite remarkable progress in nucleic acid sequencing with nanopores, its application to PTM detection in proteins remains at an early stage, hindered by challenges in protein capture, controlled unfolding, the interplay of sequence and structural heterogeneity, and diverse PTM chemistries. In this chapter, we summarize the current landscape of nanopore-based PTM identification and describe two experimental strategies that represent the most feasible near-term workflows for translating nanopore technology into practical protein PTM analysis.

Indexed as

NanoporesProtein Processing, Post-TranslationalProteinsAnimalsHumansProteinsAerolysinElectrochemistryNanoporeSingle-moleculeSulfation

Identifiers

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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.