Evidence map›Paper›PMID 42680921›Full record

ArticleNature nanotechnology2026

Nanopore-enabled time-resolved monitoring of catecholamine-related phenylalanine metabolism.

Mingqian Zhang, Ziyi Li, Wenying Hao, Yakun Yi, Ke Zhou, Lei Liu, Hai-Chen Wu

Erratum issuedAbstract read
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In one paragraph

Article in Nature nanotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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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

5 · Who and what money

Authors and funding

7 authors.

Mingqian ZhangBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Ziyi LiBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.ORCID http://orcid.org/0009-0001-6739-2876
Wenying HaoBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.ORCID http://orcid.org/0009-0007-2118-8400
Yakun YiBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.ORCID http://orcid.org/0000-0002-6069-867X
Ke ZhouBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
Lei LiuCollege of Food and Bioengineering, Xihua University, Chengdu, China. liulei@xhu.edu.cn.ORCID http://orcid.org/0000-0003-1410-2254
Hai-Chen WuBeijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China. haichenwu@iccas.ac.cn.ORCID http://orcid.org/0000-0002-4934-8521

Funding

National Natural Science Foundation of China (National Science Foundation of China) 22025407, 22427807National Natural Science Foundation of China (National Science Foundation of China) 22374151
6 · The paper itself

Abstract

Catecholamines, including dopamine, noradrenaline (also known as norepinephrine) and adrenaline (also known as epinephrine), are essential regulators of neural and endocrine function. Although they are synthesized through a branched phenylalanine metabolic pathway, direct and dynamic monitoring of the enzymatic processes governing their production has remained challenging. Here we reconstitute the complete catecholamine biosynthetic pathway from phenylalanine to adrenaline in vitro using purified enzymes and cofactors, and couple this system with nanopore-based single-molecule sensing. By integrating two orthogonal molecular recognition modalities within a single nanopore platform, we achieve highly specific detection of all metabolic intermediates and end products throughout the pathway. Real-time monitoring enables direct observation of pathway progression and regulatory perturbations at single-molecule resolution. Using this approach, we show that 6-methylisothiocyanate disrupts catecholamine biosynthesis, providing mechanistic insight into how iodotyrosine dehalogenase 1 (DEHAL1) deficiency may compromise catecholamine production. Together, this integrated enzymology and label-free nanopore sensing platform enables time-resolved dissection of neurotransmitter metabolism and regulation, and offers a general framework for studying complex biochemical pathways with single-molecule resolution.

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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.