Proteomics Methodologies: The Search of Protein Biomarkers Using Microfluidic Systems Coupled to Mass Spectrometry.

IF 4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Isabel De Figueiredo, Bernard Bartenlian, Guillaume Van der Rest, Antoine Pallandre, Frédéric Halgand
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Abstract

Protein biomarkers have been the subject of intensive studies as a target for disease diagnostics and monitoring. Indeed, biomarkers have been extensively used for personalized medicine. In biological samples, these biomarkers are most often present in low concentrations masked by a biologically complex proteome (e.g., blood) making their detection difficult. This complexity is further increased by the needs to detect proteoforms and proteome complexity such as the dynamic range of compound concentrations. The development of techniques that simultaneously pre-concentrate and identify low-abundance biomarkers in these proteomes constitutes an avant-garde approach to the early detection of pathologies. Chromatographic-based methods are widely used for protein separation, but these methods are not adapted for biomarker discovery, as they require complex sample handling due to the low biomarker concentration. Therefore, microfluidics devices have emerged as a technology to overcome these shortcomings. In terms of detection, mass spectrometry (MS) is the standard analytical tool given its high sensitivity and specificity. However, for MS, the biomarker must be introduced as pure as possible in order to avoid chemical noise and improve sensitivity. As a result, microfluidics coupled with MS has become increasingly popular in the field of biomarker discovery. This review will show the different approaches to protein enrichment using miniaturized devices and the importance of their coupling with MS.

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蛋白质组学方法:利用微流体系统耦合质谱法寻找蛋白质生物标志物。
作为疾病诊断和监测的靶点,蛋白质生物标志物一直是人们深入研究的主题。事实上,生物标志物已被广泛用于个性化医疗。在生物样品中,这些生物标志物通常以低浓度存在,被生物复杂的蛋白质组(例如血液)所掩盖,使其检测变得困难。由于需要检测蛋白质形态和蛋白质组的复杂性(如化合物浓度的动态范围),这种复杂性进一步增加。同时预先浓缩和识别这些蛋白质组中低丰度生物标志物的技术的发展构成了早期检测病理的前卫方法。基于色谱的方法被广泛用于蛋白质分离,但这些方法不适合生物标志物的发现,因为它们需要复杂的样品处理,因为生物标志物浓度低。因此,微流体装置作为一种克服这些缺点的技术而出现。在检测方面,质谱(MS)具有高灵敏度和特异性,是标准的分析工具。然而,对于MS,为了避免化学噪声和提高灵敏度,必须尽可能纯净地引入生物标志物。因此,微流体与质谱结合在生物标志物发现领域越来越受欢迎。这篇综述将展示利用小型化设备进行蛋白质富集的不同方法以及它们与质谱耦合的重要性。
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来源期刊
Proteomes
Proteomes Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
6.50
自引率
3.00%
发文量
37
审稿时长
11 weeks
期刊介绍: Proteomes (ISSN 2227-7382) is an open access, peer reviewed journal on all aspects of proteome science. Proteomes covers the multi-disciplinary topics of structural and functional biology, protein chemistry, cell biology, methodology used for protein analysis, including mass spectrometry, protein arrays, bioinformatics, HTS assays, etc. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of papers. Scope: -whole proteome analysis of any organism -disease/pharmaceutical studies -comparative proteomics -protein-ligand/protein interactions -structure/functional proteomics -gene expression -methodology -bioinformatics -applications of proteomics
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