Konstantinos Kalogeropoulos, Aleksander Moldt Haack, Elizabeta Madzharova, Antea Di Lorenzo, Rawad Hanna, Erwin M Schoof, Ulrich Auf dem Keller
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引用次数: 0
摘要
定位蛋白质组学方法改变了蛋白酶研究,并将基于质谱(MS)的降解组学研究带入了蛋白酶表征和蛋白酶信号全系统检测的前沿。液相色谱(LC)-MS/MS 仪器在灵敏度和处理量方面的巨大进步,使我们能够生成大量的位置蛋白质组学数据集,这些数据集包括蛋白酶底物裂解后的天然和蛋白质末端及新末端。然而,在数据分析和后处理步骤方面却没有取得同等程度的进展,这可以说是定位蛋白质组学工作流程中最大的瓶颈。在这里,我们介绍一种计算工具 CLIPPER 2.0,它建立在之前为基于 MS 的蛋白质端点分析开发的算法基础上,促进了肽水平的注释和数据分析。CLIPPER 2.0 可与多种样品制备工作流程和蛋白质组学搜索算法配合使用,实现快速自动的数据库信息检索、统计和网络分析,以及术语组数据集的可视化。我们通过分析 HeLa 裂解液中 GluC 和 MMP9 的裂解情况,展示了我们工具的适用性。CLIPPER 2.0 可在 https://github.com/UadKLab/CLIPPER-2.0 上获取。
CLIPPER 2.0: Peptide-Level Annotation and Data Analysis for Positional Proteomics.
Positional proteomics methodologies have transformed protease research, and have brought mass spectrometry (MS)-based degradomics studies to the forefront of protease characterization and system-wide interrogation of protease signaling. Considerable advancements in both sensitivity and throughput of liquid chromatography (LC)-MS/MS instrumentation enable the generation of enormous positional proteomics datasets of natural and protein termini and neo-termini of cleaved protease substrates. However, concomitant progress has not been observed to the same extent in data analysis and post-processing steps, arguably constituting the largest bottleneck in positional proteomics workflows. Here, we present a computational tool, CLIPPER 2.0, that builds on prior algorithms developed for MS-based protein termini analysis, facilitating peptide-level annotation and data analysis. CLIPPER 2.0 can be used with several sample preparation workflows and proteomics search algorithms and enables fast and automated database information retrieval, statistical and network analysis, as well as visualization of terminomic datasets. We demonstrate the applicability of our tool by analyzing GluC and MMP9 cleavages in HeLa lysates. CLIPPER 2.0 is available at https://github.com/UadKLab/CLIPPER-2.0.
期刊介绍:
The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action.
The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data.
Scope:
-Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights
-Novel experimental and computational technologies
-Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes
-Pathway and network analyses of signaling that focus on the roles of post-translational modifications
-Studies of proteome dynamics and quality controls, and their roles in disease
-Studies of evolutionary processes effecting proteome dynamics, quality and regulation
-Chemical proteomics, including mechanisms of drug action
-Proteomics of the immune system and antigen presentation/recognition
-Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease
-Clinical and translational studies of human diseases
-Metabolomics to understand functional connections between genes, proteins and phenotypes