尿液HILIC:临床蛋白质组学中自下而上尿液蛋白质组图谱的自动样品制备。

IF 4 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ireshyn Selvan Govender, Rethabile Mokoena, Stoyan Stoychev, Previn Naicker
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引用次数: 0

摘要

尿液提供了与患者健康状况相关的各种信息来源,由于其易于收集,因此是临床蛋白质组学的理想选择。迄今为止,大多数尿液样本制备方法缺乏分析大型临床队列所需的吞吐量。为此,我们开发了一种新的工作流程,尿液HILIC(uHLC),基于珠上蛋白质捕获、清理和消化,而不需要蛋白质沉淀或离心等瓶颈处理步骤。该工作流程应用于一项急性肾损伤(AKI)试点研究。来自临床样本和合并样本的尿液在KingFisher中进行自动样本制备™ 使用基于MagReSyn®HILIC微球的新型方法的柔性磁性处理站。为了进行基准测试,还使用基于膜上(OM)蛋白质捕获和消化工作流程的已发布方案制备了合并样品。使用耦合到Sciex 5600质谱仪的Dionex Ultimate 3000 UPLC,通过LCMS以数据独立采集(DIA)模式分析肽。数据在Spectronaut中进行了搜索™ 17.两种工作流程在合并样品中显示出相似的肽和蛋白质鉴定。uHLC工作流程更容易设置和完成,与OM方法相比,动手时间更少,手动处理步骤更少。在uHLC技术重复中观察到较低的肽和蛋白质变异系数。经过统计分析,筛选出丰度变化≥8.35倍、独特肽≥2个、错误发现率≤1%的候选蛋白质标记,并揭示了121种显著、差异丰富的蛋白质,其中一些与肾损伤有已知关联。使用这种新的工作流程获得的试点数据提供了AKI患者尿液蛋白质组的信息。有必要使用这种新型高通量方法在更大的队列中进行进一步的探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Urine-HILIC: Automated Sample Preparation for Bottom-Up Urinary Proteome Profiling in Clinical Proteomics.

Urine-HILIC: Automated Sample Preparation for Bottom-Up Urinary Proteome Profiling in Clinical Proteomics.

Urine-HILIC: Automated Sample Preparation for Bottom-Up Urinary Proteome Profiling in Clinical Proteomics.

Urine-HILIC: Automated Sample Preparation for Bottom-Up Urinary Proteome Profiling in Clinical Proteomics.

Urine provides a diverse source of information related to a patient's health status and is ideal for clinical proteomics due to its ease of collection. To date, most methods for the preparation of urine samples lack the throughput required to analyze large clinical cohorts. To this end, we developed a novel workflow, urine-HILIC (uHLC), based on an on-bead protein capture, clean-up, and digestion without the need for bottleneck processing steps such as protein precipitation or centrifugation. The workflow was applied to an acute kidney injury (AKI) pilot study. Urine from clinical samples and a pooled sample was subjected to automated sample preparation in a KingFisher™ Flex magnetic handling station using the novel approach based on MagReSyn® HILIC microspheres. For benchmarking, the pooled sample was also prepared using a published protocol based on an on-membrane (OM) protein capture and digestion workflow. Peptides were analyzed by LCMS in data-independent acquisition (DIA) mode using a Dionex Ultimate 3000 UPLC coupled to a Sciex 5600 mass spectrometer. The data were searched in Spectronaut™ 17. Both workflows showed similar peptide and protein identifications in the pooled sample. The uHLC workflow was easier to set up and complete, having less hands-on time than the OM method, with fewer manual processing steps. Lower peptide and protein coefficient of variation was observed in the uHLC technical replicates. Following statistical analysis, candidate protein markers were filtered, at ≥8.35-fold change in abundance, ≥2 unique peptides and ≤1% false discovery rate, and revealed 121 significant, differentially abundant proteins, some of which have known associations with kidney injury. The pilot data derived using this novel workflow provide information on the urinary proteome of patients with AKI. Further exploration in a larger cohort using this novel high-throughput method is warranted.

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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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