Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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
_version_ 1784764750567047168
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
work_keys_str_mv AT caixue highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT xuezhangzhi highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT wuchunlong highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT sunrui highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT qianliujia highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT yueliang highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT geweigang highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT yixiao highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT liuwei highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT chenchen highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT gaohuanhuan highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT yujing highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT xuluang highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT zhuyi highthroughputproteomicsamplepreparationusingpressurecyclingtechnology
AT guotiannan highthroughputproteomicsamplepreparationusingpressurecyclingtechnology