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Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY
Proteomic characterization of plasma is critical for the development of novel pharmacodynamic biomarkers. However, the vast dynamic range renders the profiling of proteomes extremely challenging. Here, we synthesized zeolite NaY and developed a simple and rapid method to achieve comprehensive and de...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Xi'an Jiaotong University
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257194/ https://www.ncbi.nlm.nih.gov/pubmed/37305782 http://dx.doi.org/10.1016/j.jpha.2023.04.002 |
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author | Ma, Congcong Li, Yanwei Li, Jie Song, Lei Chen, Liangyu Zhao, Na Li, Xueping Chen, Ning Long, Lixia Zhao, Jin Hou, Xin Ren, Li Yuan, Xubo |
author_facet | Ma, Congcong Li, Yanwei Li, Jie Song, Lei Chen, Liangyu Zhao, Na Li, Xueping Chen, Ning Long, Lixia Zhao, Jin Hou, Xin Ren, Li Yuan, Xubo |
author_sort | Ma, Congcong |
collection | PubMed |
description | Proteomic characterization of plasma is critical for the development of novel pharmacodynamic biomarkers. However, the vast dynamic range renders the profiling of proteomes extremely challenging. Here, we synthesized zeolite NaY and developed a simple and rapid method to achieve comprehensive and deep profiling of the plasma proteome using the plasma protein corona formed on zeolite NaY. Specifically, zeolite NaY and plasma were co-incubated to form plasma protein corona on zeolite NaY (NaY-PPC), followed by conventional protein identification using liquid chromatography-tandem mass spectrometry. NaY was able to significantly enhance the detection of low-abundance plasma proteins, minimizing the “masking” effect caused by high-abundance proteins. The relative abundance of middle- and low-abundance proteins increased substantially from 2.54% to 54.41%, and the top 20 high-abundance proteins decreased from 83.63% to 25.77%. Notably, our method can quantify approximately 4000 plasma proteins with sensitivity up to pg/mL, compared to only about 600 proteins identified from untreated plasma samples. A pilot study based on plasma samples from 30 lung adenocarcinoma patients and 15 healthy subjects demonstrated that our method could successfully distinguish between healthy and disease states. In summary, this work provides an advantageous tool for the exploration of plasma proteomics and its translational applications. |
format | Online Article Text |
id | pubmed-10257194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Xi'an Jiaotong University |
record_format | MEDLINE/PubMed |
spelling | pubmed-102571942023-06-11 Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY Ma, Congcong Li, Yanwei Li, Jie Song, Lei Chen, Liangyu Zhao, Na Li, Xueping Chen, Ning Long, Lixia Zhao, Jin Hou, Xin Ren, Li Yuan, Xubo J Pharm Anal Original Article Proteomic characterization of plasma is critical for the development of novel pharmacodynamic biomarkers. However, the vast dynamic range renders the profiling of proteomes extremely challenging. Here, we synthesized zeolite NaY and developed a simple and rapid method to achieve comprehensive and deep profiling of the plasma proteome using the plasma protein corona formed on zeolite NaY. Specifically, zeolite NaY and plasma were co-incubated to form plasma protein corona on zeolite NaY (NaY-PPC), followed by conventional protein identification using liquid chromatography-tandem mass spectrometry. NaY was able to significantly enhance the detection of low-abundance plasma proteins, minimizing the “masking” effect caused by high-abundance proteins. The relative abundance of middle- and low-abundance proteins increased substantially from 2.54% to 54.41%, and the top 20 high-abundance proteins decreased from 83.63% to 25.77%. Notably, our method can quantify approximately 4000 plasma proteins with sensitivity up to pg/mL, compared to only about 600 proteins identified from untreated plasma samples. A pilot study based on plasma samples from 30 lung adenocarcinoma patients and 15 healthy subjects demonstrated that our method could successfully distinguish between healthy and disease states. In summary, this work provides an advantageous tool for the exploration of plasma proteomics and its translational applications. Xi'an Jiaotong University 2023-05 2023-04-12 /pmc/articles/PMC10257194/ /pubmed/37305782 http://dx.doi.org/10.1016/j.jpha.2023.04.002 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Ma, Congcong Li, Yanwei Li, Jie Song, Lei Chen, Liangyu Zhao, Na Li, Xueping Chen, Ning Long, Lixia Zhao, Jin Hou, Xin Ren, Li Yuan, Xubo Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY |
title | Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY |
title_full | Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY |
title_fullStr | Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY |
title_full_unstemmed | Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY |
title_short | Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY |
title_sort | comprehensive and deep profiling of the plasma proteome with protein corona on zeolite nay |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257194/ https://www.ncbi.nlm.nih.gov/pubmed/37305782 http://dx.doi.org/10.1016/j.jpha.2023.04.002 |
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