Evidence map›Paper›PMID 41984843›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

In situ and real-time monitoring of intracellular activities in single live cells using a nanopore probe.

Xiaobin Huang, Ziyi Li, Yanling Huang, Ke Zhou, Lei Liu, Hai-Chen Wu

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 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
–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

6 authors.

Xiaobin HuangBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Ziyi LiBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Yanling HuangLaboratory of Bio-inspired Materials and Interfacial Science, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Ke ZhouBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Lei LiuCollege of Food and Bioengineering, Xihua University, Chengdu 610039, China.
Hai-Chen WuBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.ORCID 0000-0002-4934-8521

Funding

MOST | National Natural Science Foundation of China (NSFC) 22025407; 22427807MOST | National Natural Science Foundation of China (NSFC) 22374151
6 · The paper itself

Abstract

Monitoring molecular activities within single live cells is vital for understanding cellular differentiation, senescence, heterogeneity, and disease progression. However, conventional single-cell analyses often rely on micromanipulation or extraction followed by downstream measurements, which cannot capture in situ real-time dynamics. Fluorescent labeling and electrochemical methods provide temporal resolution but face limitations in labeling, substrate scope, and multiplexing. Here, we present a nanopore probe that enables real-time, multiplexed monitoring of intracellular activities in single live cells. The device integrates an aluminum oxide nanostraw membrane for molecular extraction and a glass nanopore membrane for single-channel electrical detection. Using a hippocampal neuron model of ischemia-hypoxia, we simultaneously tracked dynamic changes in intracellular glutamate, ascorbic acid, and adenosine triphosphate-three key molecules involved in oxygen-glucose deprivation-induced neuronal edema. Our findings establish this nanopore probe as a powerful platform for real-time, label-free molecular profiling at the single-cell level, opening opportunities for studying disease mechanisms and therapeutic responses.

Indexed as

NanoporesNeuronsSingle-Cell AnalysisAdenosine TriphosphateAnimalsAscorbic AcidGlutamic AcidHippocampusAdenosine TriphosphateAscorbic AcidGlutamic Acidmultiplexed detectionnanopore sensingreal-time monitoringsingle-cell analysis

Identifiers

PMID41984843
PMCPMC13099677

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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.