Issue 46, 2023

On-capillary alkylation micro-reactor: a facile strategy for proteo-metabolome profiling in the same single cells

Abstract

Single-cell multi-omics analysis can provide comprehensive insights to study cell-to-cell heterogeneity in normal and disease physiology. However, due to the lack of amplification technique, the measurement of proteome and metabolome in the same cell is challenging. Herein, a novel on-capillary alkylation micro-reactor (OCAM) was developed to achieve proteo-metabolome profiling in the same single cells, by which proteins were first covalently bound to an iodoacetic acid functionalized open-tubular capillary micro-reactor via sulfhydryl alkylation reaction, and metabolites were rapidly eluted, followed by on-column digestion of captured proteins. Compared with existing methods for low-input proteome sample preparation, OCAM exhibited improved efficiency, anti-interference ability and recovery, enabling the identification of an average of 1509 protein groups in single HeLa cells. This strategy was applied to single-cell proteo-metabolome analysis of mouse oocytes at different stages, 3457 protein groups and 171 metabolites were identified in single oocytes, which is the deepest coverage of proteome and metabolome from single mouse oocytes to date, achieving complementary characterization of metabolic patterns during oocyte maturation.

Graphical abstract: On-capillary alkylation micro-reactor: a facile strategy for proteo-metabolome profiling in the same single cells

Supplementary files

Article information

Article type
Edge Article
Submitted
26 Sep 2023
Accepted
02 Nov 2023
First published
14 Nov 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2023,14, 13495-13502

On-capillary alkylation micro-reactor: a facile strategy for proteo-metabolome profiling in the same single cells

Y. He, H. Yuan, Y. Liang, X. Liu, X. Zhang, Y. Ji, B. Zhao, K. Yang, J. Zhang, S. Zhang, Y. Zhang and L. Zhang, Chem. Sci., 2023, 14, 13495 DOI: 10.1039/D3SC05047E

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