从血浆细胞外囊泡开发生物标志物的最新蛋白质组学分析的挑战和机遇。

IF 3.9 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Proteomics Pub Date : 2025-09-16 DOI:10.1002/pmic.70036
Panshak P Dakup, Ivo Diaz Ludovico, Youngki You, Chaitra Rao, Javier Flores, Lisa M Bramer, Marian Rewers, Bobbie-Jo M Webb-Robertson, Thomas O Metz, Raghavendra G Mirmira, Emily K Sims, Ernesto S Nakayasu
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引用次数: 0

摘要

细胞外囊泡(Extracellular vesicles, EVs)是细胞分泌的膜结合颗粒,在细胞间通讯中起着至关重要的作用。ev的组成可以在应激和疾病条件下发生变化,使其成为优秀的生物标志物候选者。然而,从电动汽车中提取蛋白质信息可能具有挑战性,因为它们在复杂的生物流体中的丰度很低,而且会与污染物蛋白质和颗粒共凝。浓缩电动汽车的技术有其优势和局限性,没有一种技术能够将电动汽车纯化到完全均匀化。这可能会降低恢复速度,增加复杂性,使数据解释变得困难。在这篇观点文章中,我们探讨了更好地表征EV组成,然后在复杂样品中定量EV蛋白的概念,可能是生物标志物开发的更可行途径。尽管样品中有杂质,但质谱仪可以提供可重复的EV蛋白质组的深度覆盖。这种模式的转变为整合先进的生物信息学工具提供了机会,以完善EV蛋白质组景观,识别新的生物标志物,并简化生物标志物开发中的验证过程。通过专注于利用技术而不是实现绝对纯度,这种方法可以改变当前的做法,并为强大的生物标志物发现提供机会。在此,我们强调了实施这一理念的机遇和挑战。摘要:细胞外囊泡(EVs)作为疾病的生物标志物具有巨大的潜力,因为它们可以携带来自它们的细胞的特征和发病过程。生物流体,如血浆,是高度复杂的,并且包含许多具有与电动汽车相似的物理化学性质的成分,这使得获得纯电动汽车馏分具有挑战性。获得纯制剂的挑战是研究电动汽车的主要障碍,其成分是潜在的生物标志物。本文探讨了在复杂样品中研究EV蛋白的概念,讨论了推动这一领域向前发展的机会和需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Challenges and Opportunities in State-of-the-Art Proteomics Analysis for Biomarker Development From Plasma Extracellular Vesicles.

Extracellular vesicles (EVs) are membrane-bound particles secreted by cells, playing crucial roles in intercellular communication. The composition of EVs can undergo changes in response to stress and disease conditions, making them excellent biomarker candidates. However, extracting protein information from EVs can be challenging due to their low abundance in complex biofluids and copurification with contaminant proteins and particles. Techniques to enrich EVs have their strengths and limitations, without one being able to purify EVs to complete homogeneity. This can lead to compromised recovery rates and increased complexity, making data interpretation difficult. In this viewpoint article, we explore the concept that better characterization of EV composition, followed by quantification of EV proteins in complex samples, might be a more viable route for biomarker development. Mass spectrometers can provide reproducible deep coverage of the EV proteome, despite sample impurities. This paradigm shift presents opportunities to integrate advanced bioinformatics tools to refine the EV proteome landscape, identify novel biomarkers, and streamline validation processes in biomarker development. By focusing on leveraging technology rather than achieving absolute purity, this approach can transform current practices and open opportunities for robust biomarker discovery. Herein, we highlight not only such opportunities but also challenges to implement this concept. SUMMARY: Extracellular vesicles (EVs) have enormous potential as biomarkers of diseases, as they can carry signatures of the cells they are derived from and the pathogenesis process. Biofluids, such as blood plasma, are highly complex and contain many components with physicochemical properties similar to those of EVs, making it challenging to obtain pure EV fractions. Challenges in obtaining pure preparations represent a main hurdle for studying EVs, and their components are potential biomarkers. This article explores the concept of studying EV proteins within complex samples, discussing opportunities and needs to move this field forward.

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来源期刊
Proteomics
Proteomics 生物-生化研究方法
CiteScore
6.30
自引率
5.90%
发文量
193
审稿时长
3 months
期刊介绍: PROTEOMICS is the premier international source for information on all aspects of applications and technologies, including software, in proteomics and other "omics". The journal includes but is not limited to proteomics, genomics, transcriptomics, metabolomics and lipidomics, and systems biology approaches. Papers describing novel applications of proteomics and integration of multi-omics data and approaches are especially welcome.
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