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High-throughput proteomic analysis of extracellular vesicles from saliva by chemical probe-based array.
Shen, Ao; Feng, Xin; Wang, Dongxue; Liu, Yuanyuan; Zhang, Kaifu; Wang, Jiliang; Li, Yanan; Ali, Muhammad Mujahid; Hu, Lianghai.
Afiliação
  • Shen A; Center for Supramolecular Chemical Biology, State Key Laboratory of Supramolecular Structure and Materials, School of Life Sciences, Jilin University, Changchun, 130012, China.
  • Feng X; Center for Supramolecular Chemical Biology, State Key Laboratory of Supramolecular Structure and Materials, School of Life Sciences, Jilin University, Changchun, 130012, China.
  • Wang D; Beijing Proteome Research Center, National Center for Protein Sciences, Beijing, China; The π-HuB Project Infrastructure, International Academy of Phronesis Medicine, Guangzhou, China.
  • Liu Y; Beijing Proteome Research Center, National Center for Protein Sciences, Beijing, China; The π-HuB Project Infrastructure, International Academy of Phronesis Medicine, Guangzhou, China.
  • Zhang K; Center for Supramolecular Chemical Biology, State Key Laboratory of Supramolecular Structure and Materials, School of Life Sciences, Jilin University, Changchun, 130012, China.
  • Wang J; Center for Supramolecular Chemical Biology, State Key Laboratory of Supramolecular Structure and Materials, School of Life Sciences, Jilin University, Changchun, 130012, China.
  • Li Y; Department of Pediatrics Children's Medical Center, The First Hospital of Jilin University, Changchun, 130021, China. Electronic address: ynli@jlu.edu.cn.
  • Ali MM; State Key Laboratory of Bioelectronics, National Demonstration Center for Experimental Biomedical Engineering Education, Southeast University, Nanjing, 210096, China. Electronic address: mujahidali93@gmail.com.
  • Hu L; Center for Supramolecular Chemical Biology, State Key Laboratory of Supramolecular Structure and Materials, School of Life Sciences, Jilin University, Changchun, 130012, China. Electronic address: lianghaihu@jlu.edu.cn.
Anal Chim Acta ; 1309: 342699, 2024 Jun 22.
Article em En | MEDLINE | ID: mdl-38772652
ABSTRACT
Extracellular vesicles (EVs) are cell-released, nucleus-free particles with a double-membrane structure that effectively prevents degradation of internal components by a variety of salivary enzymes. Saliva is an easily accessible biofluid that contains a wealth of valuable information for disease diagnosis and monitoring and especially reflect respiratory and digestive tract diseases. However, the lack of efficient and high-throughput methods for proteomic analysis of salivary biomarkers poses a significant challenge. Herein, we designed a salivary EV amphiphile-dendrimer supramolecular probe (SEASP) array which enables efficient enrichment and in situ detection of EVs protein biomarkers. Detergent Tween-20 washing of SEASP arrays removes high abundance of heteroproteins from saliva well. This array shows good analytical performance in the linear range of 10 µL-150 µL (LOD = 0.4 µg protein, or 10 µL saliva), exhibiting a good recovery (80.0 %). Compared to ultracentrifugation (UC), this procedure provides simple and convenient access to high-purity EVs (1.3 × 109 particles per mg protein) with good physiological status and structure. Coupling with mass spectrometry based proteomic analysis, differentially expressed proteins as selected asthma biomarkers have been screened. Then, we validated the proteomics primary screening results through clinical samples (100 µL each) using the SEASP array. Utilizing the dual antibody fluorescence technology, SEASP enables the simultaneous high-throughput detection of two proteins. Therefore, the EVs marker protein CD81 could be used as an internal standard to normalize the number of EVs, which was stably expressed in EVs. Proteomics and array results suggested that HNRNPU (P = 4.9 * 10-6) and MUC5B (P = 4.7 * 10-11) are promising protein biomarkers for infantile asthma. HNRNPU and MUC5B may be associated with disease onset and subtypes. The SEASP arrays provide a significant advancement in the field of salivary biomarker. The array enables high-throughput in situ protein detection for highly viscous and complex biological samples. It provides a rapid, low-cost, highly specific screening procedure and experimental basis for early disease screening and diagnosis in the field of liquid biopsy.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saliva / Proteômica / Vesículas Extracelulares Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Saliva / Proteômica / Vesículas Extracelulares Idioma: En Ano de publicação: 2024 Tipo de documento: Article