Multimodal atlas of single neuron metabolic electrophysiological coupling uncovers circadian rewiring.
Paper
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The authors' code
R · 22 lines · 637 B · no license
- elec <- data.frame(elec)
- colnames(elec) <- c("Iamp","Tr","Td","Iauc","Freq")
- elec$Cluster <- as.factor(cluster)
- y_mean <- matrix(0,ncol(elec),length(clu))
- x_mean <- matrix(0,ncol(t(data)),length(clu))
- for(i in 1:length(clu)){
- y_mean[,i] <- apply(elec[cluster==clu[i],],2,function(x){mean(x)})
- x_mean[,i] <- apply(t(data)[cluster==clu[i],],2,function(x){mean(x)})
- }
- pheatmap::pheatmap(t(scale(t(y_mean))),cluster_cols = F,border_color = 'white',
- cluster_rows = F)
- x_y_mean_cor <- psych::corr.test(t(x_mean),t(y_mean))[['r']]
- x_y_mean_p <- psych::corr.test(t(x_mean),t(y_mean))[['p']]
correlation.R at commit dfb43e1, no license · at the source
Overview
- Department of Neurology, The First Affiliated Hospital of USTC, Center for Advanced Interdisciplinary Science and Biomedicine of IHM, State Key Laboratory of Eye Health, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230001, China
- Anhui Province Key Laboratory of Biomedical Imaging and Intelligent Processing, Institute of Artificial Intelligence, Hefei Comprehensive National Science Center, Hefei 230088, China
Abstract
Neuronal metabolism fundamentally modulates synaptic activity, yet how single-cell metabolic architecture aligns with electrophysiological diversity remains elusive. By integrating patch-clamp electrophysiology with single-neuron mass spectrometry (SNMS), we resolve metabolomic heterogeneity across suprachiasmatic nucleus (SCN) neurons, revealing six metabolic states with distinct synaptic dynamics, from lipid-enriched SCN1 exhibiting high-frequency presynaptic activity to quiescent SCN6. Pathway analysis linked metabolic state-specific signatures to sulfur metabolism, glutathione regulation, and citrate cycle dynamics. Machine learning and correlation networks mapped metabolites to functional parameters: histidine, carnitine, and creatinine regulated neuronal activity, validated by intracellular metabolite delivery experiments. Strikingly, light-dark cycles dynamically reconfigured most of the metabolite-postsynaptic current correlations, including light-induced taurine coupling to synaptic transmission. This multimodal platform establishes cellular metabolism as a tunable factor associated with neuronal heterogeneity and circadian plasticity, suggesting potential therapeutic avenues for circadian disorders.
Reproduced under the paper's license (CC BY-NC), from the paper cited above.
Repository
Its files are read in the Code ↔ Paper reader above.
SNMS-ctrl/SNMS
dfb43e1ff5423454273909425b5d6db1c2ae9c27, 20 February 2026Availability: 1 check, the latest on 27 September 2026: the link answers
- 27 September 2026: the link answers
4 files
- correlation.R, R, 22 lines
- heatmap.R, R, 27 lines
- regression_learning.m, MATLAB, 19 lines
- six_cluster.R, R, 17 lines
The paper's code and data availability statement is in the Data section.
Tracing map
Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.
What the map holds:
- 1 repository of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 4 scripts, each with its path and the digest of its content;
- no match between paragraphs and code yet;
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
No dataset and no data link were found in the paper.
Data and code availability
The raw single-cell mass spectrometry data and electrophysiological data generated in this study have been deposited in the MassIVE database under the accession code MassIVE: MSV000101065 and are publicly available as of the date of publication. The custom codes in this study are uploaded to GitHub (https://
Reproduced under the paper's license (CC BY-NC), from the paper cited above.
Versions
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Version 1, 27 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 3 keywords, 8 funders, 74 references.
Cite
This paper
Yuan, M., Ge, S., Qian, W., Miao, C., Liang, W., Chen, Q., Zhu, H., & Xiong, W. (2026). Multimodal atlas of single neuron metabolic electrophysiological coupling uncovers circadian rewiring. iScience, 29(7), 116337. https://
BibTeX
@article{yuan2026multimo
author = {Yuan, Man and Ge, Siyuan and Qian, Wenwei and Miao, Chenjian and Liang, Wei and Chen, Qi and Zhu, Hongying and Xiong, Wei},
title = {{Multimodal atlas of single neuron metabolic electrophysiological coupling uncovers circadian rewiring}},
journal = {iScience},
year = {2026},
month = jun,
volume = {29},
number = {7},
pages = {116337},
publisher = {Elsevier},
issn = {2589-0042},
doi = {10.1016/
url = {https://
pmid = {42325561},
pmcid = {PMC13276300}
}
RIS
TY - JOUR
AU - Yuan, Man
AU - Ge, Siyuan
AU - Qian, Wenwei
AU - Miao, Chenjian
AU - Liang, Wei
AU - Chen, Qi
AU - Zhu, Hongying
AU - Xiong, Wei
TI - Multimodal atlas of single neuron metabolic electrophysiological coupling uncovers circadian rewiring
T2 - iScience
J2 - iScience
PY - 2026
DA - 2026/
VL - 29
IS - 7
SP - 116337
SN - 2589-0042
PB - Elsevier
DO - 10.1016/
UR - https://
LA - en
ER -
CSL-JSON
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