Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry
Single-cell metabolite measurement remains highly challenging due to difficulties related to single cell isolation, metabolite detection, and identification of low levels of metabolites. Here, as a first step of the technological development, we propose a novel strategy integrating spiral inertial m...
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sg-ntu-dr.10356-1593422022-07-22T07:08:33Z Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry Zhang, Leicheng Xu, Tengfei Zhang, Jingtao Wong, Stephen Choong Chee Ritchie, Mark Hou, Han Wei Wang, Yulan Lee Kong Chian School of Medicine (LKCMedicine) School of Mechanical and Aerospace Engineering School of Civil and Environmental Engineering Singapore Phenome Centre Science::Medicine Engineering::Mechanical engineering Cell Culture Ion Mobility Spectrometers Single-cell metabolite measurement remains highly challenging due to difficulties related to single cell isolation, metabolite detection, and identification of low levels of metabolites. Here, as a first step of the technological development, we propose a novel strategy integrating spiral inertial microfluidics and ion mobility mass spectrometry (IM-MS) for single-cell metabolite detection and identification. Cells in methanol suspension are inertially focused into a single stream in the spiral microchannel. This stream of separated cells is delivered to the nanoelectrospray needle to be lysed and ionized and subsequently analyzed in real time by IM-MS. This analytical system enables six to eight single-cell metabolic fingerprints to be collected per minute, including gas-phase collisional cross section (CCS) measurements as an additional molecular descriptor, giving increased confidence in metabolite identification. As a proof of concept, the metabolic profiles of three types of cancer cells (U2OS, HepG2, and HepG2.215) were successfully screened, and 19 distinct lipids species were identified with CCS value filtering. Furthermore, principal component analysis (PCA) showed differentiation of the three cancer cell lines, mainly due to cellular surface phospholipids. Taken together, our technology platform offers a simple and efficient method for single-cell lipid profiling, with additional ion mobility separation of lipids significantly improving the confidence toward identification of metabolites. Nanyang Technological University We acknowledge the financial support from the Lee Kong Chian School of Medicine. 2022-06-15T00:35:57Z 2022-06-15T00:35:57Z 2021 Journal Article Zhang, L., Xu, T., Zhang, J., Wong, S. C. C., Ritchie, M., Hou, H. W. & Wang, Y. (2021). Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry. Analytical Chemistry, 93(30), 10462-10468. https://dx.doi.org/10.1021/acs.analchem.1c00106 0003-2700 https://hdl.handle.net/10356/159342 10.1021/acs.analchem.1c00106 34289696 2-s2.0-85112392092 30 93 10462 10468 en Analytical Chemistry © 2021 American Chemical Society. All rights reserved. |
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Science::Medicine Engineering::Mechanical engineering Cell Culture Ion Mobility Spectrometers Zhang, Leicheng Xu, Tengfei Zhang, Jingtao Wong, Stephen Choong Chee Ritchie, Mark Hou, Han Wei Wang, Yulan Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
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Single-cell metabolite measurement remains highly challenging due to difficulties related to single cell isolation, metabolite detection, and identification of low levels of metabolites. Here, as a first step of the technological development, we propose a novel strategy integrating spiral inertial microfluidics and ion mobility mass spectrometry (IM-MS) for single-cell metabolite detection and identification. Cells in methanol suspension are inertially focused into a single stream in the spiral microchannel. This stream of separated cells is delivered to the nanoelectrospray needle to be lysed and ionized and subsequently analyzed in real time by IM-MS. This analytical system enables six to eight single-cell metabolic fingerprints to be collected per minute, including gas-phase collisional cross section (CCS) measurements as an additional molecular descriptor, giving increased confidence in metabolite identification. As a proof of concept, the metabolic profiles of three types of cancer cells (U2OS, HepG2, and HepG2.215) were successfully screened, and 19 distinct lipids species were identified with CCS value filtering. Furthermore, principal component analysis (PCA) showed differentiation of the three cancer cell lines, mainly due to cellular surface phospholipids. Taken together, our technology platform offers a simple and efficient method for single-cell lipid profiling, with additional ion mobility separation of lipids significantly improving the confidence toward identification of metabolites. |
author2 |
Lee Kong Chian School of Medicine (LKCMedicine) |
author_facet |
Lee Kong Chian School of Medicine (LKCMedicine) Zhang, Leicheng Xu, Tengfei Zhang, Jingtao Wong, Stephen Choong Chee Ritchie, Mark Hou, Han Wei Wang, Yulan |
format |
Article |
author |
Zhang, Leicheng Xu, Tengfei Zhang, Jingtao Wong, Stephen Choong Chee Ritchie, Mark Hou, Han Wei Wang, Yulan |
author_sort |
Zhang, Leicheng |
title |
Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
title_short |
Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
title_full |
Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
title_fullStr |
Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
title_full_unstemmed |
Single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
title_sort |
single cell metabolite detection using inertial microfluidics-assisted ion mobility mass spectrometry |
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2022 |
url |
https://hdl.handle.net/10356/159342 |
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1739837436032188416 |