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Mol Cell Proteomics ; 23(6): 100781, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38703894

RESUMO

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.


Assuntos
Peptídeos , Proteômica , Espectrometria de Massas em Tandem , Proteômica/métodos , Humanos , Peptídeos/metabolismo , Peptídeos/análise , Células HeLa , Espectrometria de Massas em Tandem/métodos , Algoritmos , Software , Bases de Dados de Proteínas , Cromatografia Líquida , Anotação de Sequência Molecular , Análise de Dados , Metaloproteinase 9 da Matriz/metabolismo
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