Protein and peptide profiling as a tool for biomarker discovery in depression

IF 2.5 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Khaled AlAwam, Ed Dudley, Rossen Donev, Johannes Thome
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引用次数: 22

Abstract

This study sought to determine whether protein and/or peptide profiles from serum were able to distinguish patients suffering from depression from healthy control subjects and thereby act as biomarker candidates with potential diagnostic value. Serum samples were collected from patients (n = 39) and controls (n = 30). A C8 magnetic bead protocol was used to prepare serum proteins, while a microextraction C18 packed tip was used to isolate serum peptides. Both protein and peptide profiles were recorded by MALDI-MS and the data were exported for further analysis. No protein signals differentiated patients from controls and principle component analysis of the entire peptide profile did not allow for distinct clustering of the two groups. Further analysis of individual peptides however identified three peptide signals whose intensities were significantly different between patients and control subjects. The efficacy of these potential biomarker candidates to identify the patients was therefore studied using a receiver operating characteristic (ROC) curve and the combined use of all three candidates together offered the most specific and sensitive identification of true positive cases of depression.

蛋白质和肽谱分析作为发现抑郁症生物标志物的工具
本研究旨在确定血清中的蛋白质和/或肽谱是否能够区分抑郁症患者和健康对照者,从而作为具有潜在诊断价值的生物标志物候选物。收集患者(n = 39)和对照组(n = 30)的血清样本。采用C8磁珠制备血清蛋白,采用微萃取C18包装尖端分离血清肽。用MALDI-MS记录蛋白质和肽谱,并导出数据供进一步分析。没有蛋白质信号将患者与对照组区分开来,整个肽谱的主成分分析不允许两组的明显聚类。然而,对单个肽的进一步分析确定了三种肽信号,其强度在患者和对照组之间存在显著差异。因此,使用受试者工作特征(ROC)曲线研究了这些潜在的候选生物标志物识别患者的功效,并将所有三种候选生物标志物结合使用,提供了对真阳性抑郁症病例最具体和最敏感的识别。
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来源期刊
ELECTROPHORESIS
ELECTROPHORESIS 生物-分析化学
CiteScore
6.30
自引率
13.80%
发文量
244
审稿时长
1.9 months
期刊介绍: ELECTROPHORESIS is an international journal that publishes original manuscripts on all aspects of electrophoresis, and liquid phase separations (e.g., HPLC, micro- and nano-LC, UHPLC, micro- and nano-fluidics, liquid-phase micro-extractions, etc.). Topics include new or improved analytical and preparative methods, sample preparation, development of theory, and innovative applications of electrophoretic and liquid phase separations methods in the study of nucleic acids, proteins, carbohydrates natural products, pharmaceuticals, food analysis, environmental species and other compounds of importance to the life sciences. Papers in the areas of microfluidics and proteomics, which are not limited to electrophoresis-based methods, will also be accepted for publication. Contributions focused on hyphenated and omics techniques are also of interest. Proteomics is within the scope, if related to its fundamentals and new technical approaches. Proteomics applications are only considered in particular cases. Papers describing the application of standard electrophoretic methods will not be considered. Papers on nanoanalysis intended for publication in ELECTROPHORESIS should focus on one or more of the following topics: • Nanoscale electrokinetics and phenomena related to electric double layer and/or confinement in nano-sized geometry • Single cell and subcellular analysis • Nanosensors and ultrasensitive detection aspects (e.g., involving quantum dots, "nanoelectrodes" or nanospray MS) • Nanoscale/nanopore DNA sequencing (next generation sequencing) • Micro- and nanoscale sample preparation • Nanoparticles and cells analyses by dielectrophoresis • Separation-based analysis using nanoparticles, nanotubes and nanowires.
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