Comprehensive and deep profiling of the plasma proteome with protein corona on zeolite NaY

被引:3
|
作者
Ma, Congcong [1 ]
Li, Yanwei [2 ]
Li, Jie [3 ]
Song, Lei [3 ]
Chen, Liangyu [3 ]
Zhao, Na [3 ]
Li, Xueping [1 ]
Chen, Ning [1 ]
Long, Lixia [1 ]
Zhao, Jin [1 ]
Hou, Xin [1 ]
Ren, Li [4 ]
Yuan, Xubo [1 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin Key Lab Composite & Funct Mat, Tianjin 300350, Peoples R China
[2] Tianjin Med Univ Canc Inst & Hosp, Dept Integrat Oncol, Tianjin 300060, Peoples R China
[3] Tianjin Key Lab Clin Multi, Dept Prote, Tianjin 300308, Peoples R China
[4] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Tianjins Clin Res Ctr Canc, Dept Clin Lab,Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
基金
中国国家自然科学基金;
关键词
NaY; Plasma proteomics; Protein corona; Low -abundance proteins; OF-THE-ART; MASS-SPECTROMETRY; BIOMARKER DISCOVERY; ABUNDANCE PROTEINS; ADSORPTION; DEPLETION; CHROMATOGRAPHY; ENRICHMENT; STRATEGY; WORKFLOW;
D O I
10.1016/j.jpha.2023.04.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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/).
引用
收藏
页码:503 / 513
页数:11
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