期刊
JOURNAL OF PHARMACEUTICAL ANALYSIS
卷 13, 期 5, 页码 503-513出版社
ELSEVIER
DOI: 10.1016/j.jpha.2023.04.002
关键词
NaY; Plasma proteomics; Protein corona; Low -abundance proteins
This study synthesized zeolite NaY and developed a method to comprehensively profile plasma proteome using the plasma protein corona formed on zeolite NaY, which is important for the development of novel pharmacodynamic biomarkers.
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 middleand low-abundance proteins increased substantially from 2.54% to 54.41%, and the top 20 highabundance 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. & COPY; 2023 The Author(s). Published by Elsevier B.V. on behalf of Xi'an Jiaotong University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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