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High-throughput proteomic sample preparation using pressure cycling technology
High-throughput lysis and proteolytic digestion of biopsy-level tissue specimens is a major bottleneck for clinical proteomics. Here we describe a detailed protocol of pressure cycling technology (PCT)-assisted sample preparation for proteomic analysis of biopsy tissues. A piece of fresh frozen or f...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362583/ https://www.ncbi.nlm.nih.gov/pubmed/35931778 http://dx.doi.org/10.1038/s41596-022-00727-1 |
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author | Cai, Xue Xue, Zhangzhi Wu, Chunlong Sun, Rui Qian, Liujia Yue, Liang Ge, Weigang Yi, Xiao Liu, Wei Chen, Chen Gao, Huanhuan Yu, Jing Xu, Luang Zhu, Yi Guo, Tiannan |
author_facet | Cai, Xue Xue, Zhangzhi Wu, Chunlong Sun, Rui Qian, Liujia Yue, Liang Ge, Weigang Yi, Xiao Liu, Wei Chen, Chen Gao, Huanhuan Yu, Jing Xu, Luang Zhu, Yi Guo, Tiannan |
author_sort | Cai, Xue |
collection | PubMed |
description | High-throughput lysis and proteolytic digestion of biopsy-level tissue specimens is a major bottleneck for clinical proteomics. Here we describe a detailed protocol of pressure cycling technology (PCT)-assisted sample preparation for proteomic analysis of biopsy tissues. A piece of fresh frozen or formalin-fixed paraffin-embedded tissue weighing ~0.1–2 mg is placed in a 150 μL pressure-resistant tube called a PCT-MicroTube with proper lysis buffer. After closing with a PCT-MicroPestle, a batch of 16 PCT-MicroTubes are placed in a Barocycler, which imposes oscillating pressure to the samples from one atmosphere to up to ~3,000 times atmospheric pressure. The pressure cycling schemes are optimized for tissue lysis and protein digestion, and can be programmed in the Barocycler to allow reproducible, robust and efficient protein extraction and proteolysis digestion for mass spectrometry-based proteomics. This method allows effective preparation of not only fresh frozen and formalin-fixed paraffin-embedded tissue, but also cells, feces and tear strips. It takes ~3 h to process 16 samples in one batch. The resulting peptides can be analyzed by various mass spectrometry-based proteomics methods. We demonstrate the applications of this protocol with mouse kidney tissue and eight types of human tumors. |
format | Online Article Text |
id | pubmed-9362583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93625832022-08-10 High-throughput proteomic sample preparation using pressure cycling technology Cai, Xue Xue, Zhangzhi Wu, Chunlong Sun, Rui Qian, Liujia Yue, Liang Ge, Weigang Yi, Xiao Liu, Wei Chen, Chen Gao, Huanhuan Yu, Jing Xu, Luang Zhu, Yi Guo, Tiannan Nat Protoc Protocol High-throughput lysis and proteolytic digestion of biopsy-level tissue specimens is a major bottleneck for clinical proteomics. Here we describe a detailed protocol of pressure cycling technology (PCT)-assisted sample preparation for proteomic analysis of biopsy tissues. A piece of fresh frozen or formalin-fixed paraffin-embedded tissue weighing ~0.1–2 mg is placed in a 150 μL pressure-resistant tube called a PCT-MicroTube with proper lysis buffer. After closing with a PCT-MicroPestle, a batch of 16 PCT-MicroTubes are placed in a Barocycler, which imposes oscillating pressure to the samples from one atmosphere to up to ~3,000 times atmospheric pressure. The pressure cycling schemes are optimized for tissue lysis and protein digestion, and can be programmed in the Barocycler to allow reproducible, robust and efficient protein extraction and proteolysis digestion for mass spectrometry-based proteomics. This method allows effective preparation of not only fresh frozen and formalin-fixed paraffin-embedded tissue, but also cells, feces and tear strips. It takes ~3 h to process 16 samples in one batch. The resulting peptides can be analyzed by various mass spectrometry-based proteomics methods. We demonstrate the applications of this protocol with mouse kidney tissue and eight types of human tumors. Nature Publishing Group UK 2022-08-05 2022 /pmc/articles/PMC9362583/ /pubmed/35931778 http://dx.doi.org/10.1038/s41596-022-00727-1 Text en © Springer Nature Limited 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Protocol Cai, Xue Xue, Zhangzhi Wu, Chunlong Sun, Rui Qian, Liujia Yue, Liang Ge, Weigang Yi, Xiao Liu, Wei Chen, Chen Gao, Huanhuan Yu, Jing Xu, Luang Zhu, Yi Guo, Tiannan High-throughput proteomic sample preparation using pressure cycling technology |
title | High-throughput proteomic sample preparation using pressure cycling technology |
title_full | High-throughput proteomic sample preparation using pressure cycling technology |
title_fullStr | High-throughput proteomic sample preparation using pressure cycling technology |
title_full_unstemmed | High-throughput proteomic sample preparation using pressure cycling technology |
title_short | High-throughput proteomic sample preparation using pressure cycling technology |
title_sort | high-throughput proteomic sample preparation using pressure cycling technology |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9362583/ https://www.ncbi.nlm.nih.gov/pubmed/35931778 http://dx.doi.org/10.1038/s41596-022-00727-1 |
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