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High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip
Global quantification of protein abundances in single cells could provide direct information on cellular phenotypes and complement transcriptomics measurements. However, single-cell proteomics is still immature and confronts many technical challenges. Herein we describe a nested nanoPOTS (N2) chip t...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556371/ https://www.ncbi.nlm.nih.gov/pubmed/34716329 http://dx.doi.org/10.1038/s41467-021-26514-2 |
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author | Woo, Jongmin Williams, Sarah M. Markillie, Lye Meng Feng, Song Tsai, Chia-Feng Aguilera-Vazquez, Victor Sontag, Ryan L. Moore, Ronald J. Hu, Dehong Mehta, Hardeep S. Cantlon-Bruce, Joshua Liu, Tao Adkins, Joshua N. Smith, Richard D. Clair, Geremy C. Pasa-Tolic, Ljiljana Zhu, Ying |
author_facet | Woo, Jongmin Williams, Sarah M. Markillie, Lye Meng Feng, Song Tsai, Chia-Feng Aguilera-Vazquez, Victor Sontag, Ryan L. Moore, Ronald J. Hu, Dehong Mehta, Hardeep S. Cantlon-Bruce, Joshua Liu, Tao Adkins, Joshua N. Smith, Richard D. Clair, Geremy C. Pasa-Tolic, Ljiljana Zhu, Ying |
author_sort | Woo, Jongmin |
collection | PubMed |
description | Global quantification of protein abundances in single cells could provide direct information on cellular phenotypes and complement transcriptomics measurements. However, single-cell proteomics is still immature and confronts many technical challenges. Herein we describe a nested nanoPOTS (N2) chip to improve protein recovery, operation robustness, and processing throughput for isobaric-labeling-based scProteomics workflow. The N2 chip reduces reaction volume to <30 nL and increases capacity to >240 single cells on a single microchip. The tandem mass tag (TMT) pooling step is simplified by adding a microliter droplet on the nested nanowells to combine labeled single-cell samples. In the analysis of ~100 individual cells from three different cell lines, we demonstrate that the N2 chip-based scProteomics platform can robustly quantify ~1500 proteins and reveal membrane protein markers. Our analyses also reveal low protein abundance variations, suggesting the single-cell proteome profiles are highly stable for the cells cultured under identical conditions. |
format | Online Article Text |
id | pubmed-8556371 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85563712021-11-15 High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip Woo, Jongmin Williams, Sarah M. Markillie, Lye Meng Feng, Song Tsai, Chia-Feng Aguilera-Vazquez, Victor Sontag, Ryan L. Moore, Ronald J. Hu, Dehong Mehta, Hardeep S. Cantlon-Bruce, Joshua Liu, Tao Adkins, Joshua N. Smith, Richard D. Clair, Geremy C. Pasa-Tolic, Ljiljana Zhu, Ying Nat Commun Article Global quantification of protein abundances in single cells could provide direct information on cellular phenotypes and complement transcriptomics measurements. However, single-cell proteomics is still immature and confronts many technical challenges. Herein we describe a nested nanoPOTS (N2) chip to improve protein recovery, operation robustness, and processing throughput for isobaric-labeling-based scProteomics workflow. The N2 chip reduces reaction volume to <30 nL and increases capacity to >240 single cells on a single microchip. The tandem mass tag (TMT) pooling step is simplified by adding a microliter droplet on the nested nanowells to combine labeled single-cell samples. In the analysis of ~100 individual cells from three different cell lines, we demonstrate that the N2 chip-based scProteomics platform can robustly quantify ~1500 proteins and reveal membrane protein markers. Our analyses also reveal low protein abundance variations, suggesting the single-cell proteome profiles are highly stable for the cells cultured under identical conditions. Nature Publishing Group UK 2021-10-29 /pmc/articles/PMC8556371/ /pubmed/34716329 http://dx.doi.org/10.1038/s41467-021-26514-2 Text en © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Woo, Jongmin Williams, Sarah M. Markillie, Lye Meng Feng, Song Tsai, Chia-Feng Aguilera-Vazquez, Victor Sontag, Ryan L. Moore, Ronald J. Hu, Dehong Mehta, Hardeep S. Cantlon-Bruce, Joshua Liu, Tao Adkins, Joshua N. Smith, Richard D. Clair, Geremy C. Pasa-Tolic, Ljiljana Zhu, Ying High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
title | High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
title_full | High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
title_fullStr | High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
title_full_unstemmed | High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
title_short | High-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
title_sort | high-throughput and high-efficiency sample preparation for single-cell proteomics using a nested nanowell chip |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556371/ https://www.ncbi.nlm.nih.gov/pubmed/34716329 http://dx.doi.org/10.1038/s41467-021-26514-2 |
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